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Browsing by Author "Afshin, Ashkan (57217465455)"

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    Publication
    Burden of diarrhea in the eastern mediterranean region, 1990-2013: Findings from the global burden of disease study 2013
    (2016)
    Khalil, Ibrahim (58255049500)
    ;
    Colombara, Danny V. (37025591000)
    ;
    Forouzanfar, Mohammad Hossein (57202562738)
    ;
    Troeger, Christopher (57195223624)
    ;
    Daoud, Farah (57201079837)
    ;
    Moradi-Lakeh, Maziar (35617421300)
    ;
    El Bcheraoui, Charbel (25027689700)
    ;
    Rao, Puja C. (57191835613)
    ;
    Afshin, Ashkan (57217465455)
    ;
    Charara, Raghid (56514085300)
    ;
    Abate, Kalkidan Hassen (57207943858)
    ;
    Abd El Razek, Mohammed Magdy (57192379650)
    ;
    Abd-Allah, Foad (36503428900)
    ;
    Abu-Elyazeed, Remon (57224428155)
    ;
    Kiadaliri, Aliasghar Ahmad (57199100665)
    ;
    Akanda, Ali Shafqat (35290419100)
    ;
    Akseer, Nadia (57207801968)
    ;
    Alam, Khurshid (57203681299)
    ;
    Alasfoor, Deena (57211114684)
    ;
    Ali, Raghib (57196506541)
    ;
    AlMazroa, Mohammad A. (35572530900)
    ;
    Alomari, Mahmoud A. (57219982609)
    ;
    Salem Al-Raddadi, Rajaa Mohammad (57192371411)
    ;
    Alsharif, Ubai (57211633255)
    ;
    Alsowaidi, Shirina (26867516400)
    ;
    Altirkawi, Khalid A. (57202762923)
    ;
    Alvis-Guzman, Nelson (57210741239)
    ;
    Ammar, Walid (57208159281)
    ;
    Antonio, Carl Abelardo T. (55247644500)
    ;
    Asayesh, Hamid (55334322800)
    ;
    Asghar, Rana Jawad (57209013760)
    ;
    Atique, Suleman (56505419100)
    ;
    Awasthi, Ashish (57200155811)
    ;
    Bacha, Umar (57200173721)
    ;
    Badawi, Alaa (57216776029)
    ;
    Barac, Aleksandra (55550748700)
    ;
    Bedi, Neeraj (57988442200)
    ;
    Bekele, Tolesa (57195086149)
    ;
    Bensenor, Isabela M. (7004830338)
    ;
    Betsu, Balem Demtsu (57196316128)
    ;
    Bhutta, Zulfiqar (24342648300)
    ;
    Abdulhak, Aref A. Bin (57201757922)
    ;
    Butt, Zahid A. (57202522739)
    ;
    Danawi, Hadi (57201079895)
    ;
    Dubey, Manisha (57219898654)
    ;
    Endries, Aman Yesuf (57216324852)
    ;
    Faghmous, Imad M.D.A. (57190290003)
    ;
    Farid, Talha (24824364300)
    ;
    Farvid, Maryam S. (8273562500)
    ;
    Farzadfar, Farshad (57195049611)
    ;
    Fereshtehnejad, Seyed-Mohammad (57202557520)
    ;
    Fischer, Florian (55508208800)
    ;
    Anderson Fitchett, Joseph Robert (57192378614)
    ;
    Gibney, Katherine B. (57202564104)
    ;
    Mohamed Ginawi, Ibrahim Abdelmageem (57192378390)
    ;
    Gishu, Melkamu Dedefo (57190277898)
    ;
    Gugnani, Harish Chander (7005567008)
    ;
    Gupta, Rahul (57204120071)
    ;
    Hailu, Gessessew Bugssa (57219637263)
    ;
    Hamadeh, Randah Ribhi (57202769526)
    ;
    Hamidi, Samer (24366336000)
    ;
    Harb, Hilda L. (57221443122)
    ;
    Hedayati, Mohammad T. (23979915700)
    ;
    Hsairi, Mohamed (57209033943)
    ;
    Husseini, Abdullatif (6603689690)
    ;
    Jahanmehr, Nader (57203122718)
    ;
    Javanbakht, Mehdi (57204619886)
    ;
    Jibat, Tariku (57201181881)
    ;
    Jonas, Jost B. (7202492953)
    ;
    Kasaeian, Amir (57195540738)
    ;
    Khader, Yousef Saleh (55654192600)
    ;
    Khan, Abdur Rahman (55520620000)
    ;
    Khan, Ejaz Ahmad (57218791274)
    ;
    Khan, Gulfaraz (6701635515)
    ;
    Khoja, Tawfik Ahmed Muthafer (7003561381)
    ;
    Kinfu, Yohannes (12770281900)
    ;
    Kissoon, Niranjan (7006364038)
    ;
    Koyanagi, Ai (57197741912)
    ;
    Lal, Aparna (55163011100)
    ;
    Abdul Latif, Asma Abdul (57192380848)
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    Lunevicius, Raimundas (57216165063)
    ;
    Abd El Razek, Hassan Magdy (57195948985)
    ;
    Majeed, Azeem (7102027801)
    ;
    Malekzadeh, Reza (7005197760)
    ;
    Mehari, Alem (57211114616)
    ;
    Mekonnen, Alemayehu B. (57200179648)
    ;
    Melaku, Yohannes Adama (57203122720)
    ;
    Memish, Ziad A. (7005059350)
    ;
    Mendoza, Walter (57216905642)
    ;
    Misganaw, Awoke (57202808713)
    ;
    Ibrahim Mohamed, Layla Abdalla (57192381009)
    ;
    Nachega, Jean B. (6701544088)
    ;
    Nguyen, Quyen Le (57223642100)
    ;
    Nisar, Muhammad Imran (57191774461)
    ;
    Peprah, Emmanuel Kwame (57195257834)
    ;
    Platts-Mills, James A. (8540918800)
    ;
    Pourmalek, Farshad (8309390500)
    ;
    Qorbani, Mostafa (24831040300)
    ;
    Rafay, Anwar (57212263323)
    ;
    Rahimi-Movaghar, Vafa (6507646446)
    ;
    Ur Rahman, Sajjad (15835524800)
    ;
    Rai, Rajesh Kumar (51864423900)
    ;
    Rana, Saleem M. (57204884092)
    ;
    Ranabhat, Chhabi L. (56719695500)
    ;
    Rao, Sowmya R. (15760668600)
    ;
    Refaat, Amany H. (57216641565)
    ;
    Riddle, Mark (7102072160)
    ;
    Roshandel, Gholamreza (14034446800)
    ;
    Ruhago, George Mugambage (50761517500)
    ;
    Saleh, Muhammad Muhammad (57190288485)
    ;
    Sanabria, Juan R. (7006262917)
    ;
    Sawhney, Monika (57217153893)
    ;
    Sepanlou, Sadaf G. (36248136000)
    ;
    Setegn, Tesfaye (37075667700)
    ;
    Sliwa, Karen (57207223988)
    ;
    Sreeramareddy, Chandrashekhar T. (57212263335)
    ;
    Sykes, Bryan L. (57211183396)
    ;
    Tavakkoli, Mohammad (57202524239)
    ;
    Tedla, Bemnet Amare (57211142920)
    ;
    Terkawi, Abdullah S. (57211144258)
    ;
    Ukwaja, Kingsley (57202824584)
    ;
    Uthman, Olalekan A. (23026328100)
    ;
    Westerman, Ronny (57218361023)
    ;
    Wubshet, Mamo (54409732600)
    ;
    Yenesew, Muluken A. (39361108000)
    ;
    Yonemoto, Naohiro (57204947657)
    ;
    Younis, Mustafa Z. (8549393000)
    ;
    Zaidi, Zoubida (57197376721)
    ;
    El Sayed Zaki, Maysaa (57203666922)
    ;
    Al Rabeeah, Abdullah A. (6603625258)
    ;
    Wang, Haidong (16507828100)
    ;
    Naghavi, Mohsen (57207906323)
    ;
    Vos, Theo (57223885848)
    ;
    Lopez, Alan D. (7401455668)
    ;
    Murray, Christopher J. L. (55481130700)
    ;
    Mokdad, Ali H. (7004813962)
    Diarrheal diseases (DD) are leading causes of disease burden, death, and disability, especially in children in low-income settings. DD can also impact a child's potential livelihood through stunted physical growth, cognitive impairment, and other sequelae. As part of the Global Burden of Disease Study, we estimated DD burden, and the burden attributable to specific risk factors and particular etiologies, in the Eastern Mediterranean Region (EMR) between 1990 and 2013. For both sexes and all ages, we calculated disability-adjusted life years (DALYs), which are the sum of years of life lost and years lived with disability. We estimate that over 125,000 deaths (3.6% of total deaths) were due to DD in the EMR in 2013, with a greater burden of DD in low-and middle-income countries. Diarrhea deaths per 100,000 children under 5 years of age ranged from one (95% uncertainty interval [UI] = 0-1) in Bahrain and Oman to 471 (95% UI = 245-763) in Somalia. The pattern for diarrhea DALYs among those under 5 years of age closely followed that for diarrheal deaths. DALYs per 100,000 ranged from 739 (95% UI = 520-989) in Syria to 40,869 (95% UI = 21,540-65,823) in Somalia. Our results highlighted a highly inequitable burden of DD in EMR, mainly driven by the lack of access to proper resources such as water and sanitation. Our findings will guide preventive and treatment interventions which are based on evidence and which follow the ultimate goal of reducing the DD burden. Copyright © 2016 by The American Society of Tropical Medicine and Hygiene.
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    Publication
    Burden of diarrhea in the eastern mediterranean region, 1990-2013: Findings from the global burden of disease study 2013
    (2016)
    Khalil, Ibrahim (58255049500)
    ;
    Colombara, Danny V. (37025591000)
    ;
    Forouzanfar, Mohammad Hossein (57202562738)
    ;
    Troeger, Christopher (57195223624)
    ;
    Daoud, Farah (57201079837)
    ;
    Moradi-Lakeh, Maziar (35617421300)
    ;
    El Bcheraoui, Charbel (25027689700)
    ;
    Rao, Puja C. (57191835613)
    ;
    Afshin, Ashkan (57217465455)
    ;
    Charara, Raghid (56514085300)
    ;
    Abate, Kalkidan Hassen (57207943858)
    ;
    Abd El Razek, Mohammed Magdy (57192379650)
    ;
    Abd-Allah, Foad (36503428900)
    ;
    Abu-Elyazeed, Remon (57224428155)
    ;
    Kiadaliri, Aliasghar Ahmad (57199100665)
    ;
    Akanda, Ali Shafqat (35290419100)
    ;
    Akseer, Nadia (57207801968)
    ;
    Alam, Khurshid (57203681299)
    ;
    Alasfoor, Deena (57211114684)
    ;
    Ali, Raghib (57196506541)
    ;
    AlMazroa, Mohammad A. (35572530900)
    ;
    Alomari, Mahmoud A. (57219982609)
    ;
    Salem Al-Raddadi, Rajaa Mohammad (57192371411)
    ;
    Alsharif, Ubai (57211633255)
    ;
    Alsowaidi, Shirina (26867516400)
    ;
    Altirkawi, Khalid A. (57202762923)
    ;
    Alvis-Guzman, Nelson (57210741239)
    ;
    Ammar, Walid (57208159281)
    ;
    Antonio, Carl Abelardo T. (55247644500)
    ;
    Asayesh, Hamid (55334322800)
    ;
    Asghar, Rana Jawad (57209013760)
    ;
    Atique, Suleman (56505419100)
    ;
    Awasthi, Ashish (57200155811)
    ;
    Bacha, Umar (57200173721)
    ;
    Badawi, Alaa (57216776029)
    ;
    Barac, Aleksandra (55550748700)
    ;
    Bedi, Neeraj (57988442200)
    ;
    Bekele, Tolesa (57195086149)
    ;
    Bensenor, Isabela M. (7004830338)
    ;
    Betsu, Balem Demtsu (57196316128)
    ;
    Bhutta, Zulfiqar (24342648300)
    ;
    Abdulhak, Aref A. Bin (57201757922)
    ;
    Butt, Zahid A. (57202522739)
    ;
    Danawi, Hadi (57201079895)
    ;
    Dubey, Manisha (57219898654)
    ;
    Endries, Aman Yesuf (57216324852)
    ;
    Faghmous, Imad M.D.A. (57190290003)
    ;
    Farid, Talha (24824364300)
    ;
    Farvid, Maryam S. (8273562500)
    ;
    Farzadfar, Farshad (57195049611)
    ;
    Fereshtehnejad, Seyed-Mohammad (57202557520)
    ;
    Fischer, Florian (55508208800)
    ;
    Anderson Fitchett, Joseph Robert (57192378614)
    ;
    Gibney, Katherine B. (57202564104)
    ;
    Mohamed Ginawi, Ibrahim Abdelmageem (57192378390)
    ;
    Gishu, Melkamu Dedefo (57190277898)
    ;
    Gugnani, Harish Chander (7005567008)
    ;
    Gupta, Rahul (57204120071)
    ;
    Hailu, Gessessew Bugssa (57219637263)
    ;
    Hamadeh, Randah Ribhi (57202769526)
    ;
    Hamidi, Samer (24366336000)
    ;
    Harb, Hilda L. (57221443122)
    ;
    Hedayati, Mohammad T. (23979915700)
    ;
    Hsairi, Mohamed (57209033943)
    ;
    Husseini, Abdullatif (6603689690)
    ;
    Jahanmehr, Nader (57203122718)
    ;
    Javanbakht, Mehdi (57204619886)
    ;
    Jibat, Tariku (57201181881)
    ;
    Jonas, Jost B. (7202492953)
    ;
    Kasaeian, Amir (57195540738)
    ;
    Khader, Yousef Saleh (55654192600)
    ;
    Khan, Abdur Rahman (55520620000)
    ;
    Khan, Ejaz Ahmad (57218791274)
    ;
    Khan, Gulfaraz (6701635515)
    ;
    Khoja, Tawfik Ahmed Muthafer (7003561381)
    ;
    Kinfu, Yohannes (12770281900)
    ;
    Kissoon, Niranjan (7006364038)
    ;
    Koyanagi, Ai (57197741912)
    ;
    Lal, Aparna (55163011100)
    ;
    Abdul Latif, Asma Abdul (57192380848)
    ;
    Lunevicius, Raimundas (57216165063)
    ;
    Abd El Razek, Hassan Magdy (57195948985)
    ;
    Majeed, Azeem (7102027801)
    ;
    Malekzadeh, Reza (7005197760)
    ;
    Mehari, Alem (57211114616)
    ;
    Mekonnen, Alemayehu B. (57200179648)
    ;
    Melaku, Yohannes Adama (57203122720)
    ;
    Memish, Ziad A. (7005059350)
    ;
    Mendoza, Walter (57216905642)
    ;
    Misganaw, Awoke (57202808713)
    ;
    Ibrahim Mohamed, Layla Abdalla (57192381009)
    ;
    Nachega, Jean B. (6701544088)
    ;
    Nguyen, Quyen Le (57223642100)
    ;
    Nisar, Muhammad Imran (57191774461)
    ;
    Peprah, Emmanuel Kwame (57195257834)
    ;
    Platts-Mills, James A. (8540918800)
    ;
    Pourmalek, Farshad (8309390500)
    ;
    Qorbani, Mostafa (24831040300)
    ;
    Rafay, Anwar (57212263323)
    ;
    Rahimi-Movaghar, Vafa (6507646446)
    ;
    Ur Rahman, Sajjad (15835524800)
    ;
    Rai, Rajesh Kumar (51864423900)
    ;
    Rana, Saleem M. (57204884092)
    ;
    Ranabhat, Chhabi L. (56719695500)
    ;
    Rao, Sowmya R. (15760668600)
    ;
    Refaat, Amany H. (57216641565)
    ;
    Riddle, Mark (7102072160)
    ;
    Roshandel, Gholamreza (14034446800)
    ;
    Ruhago, George Mugambage (50761517500)
    ;
    Saleh, Muhammad Muhammad (57190288485)
    ;
    Sanabria, Juan R. (7006262917)
    ;
    Sawhney, Monika (57217153893)
    ;
    Sepanlou, Sadaf G. (36248136000)
    ;
    Setegn, Tesfaye (37075667700)
    ;
    Sliwa, Karen (57207223988)
    ;
    Sreeramareddy, Chandrashekhar T. (57212263335)
    ;
    Sykes, Bryan L. (57211183396)
    ;
    Tavakkoli, Mohammad (57202524239)
    ;
    Tedla, Bemnet Amare (57211142920)
    ;
    Terkawi, Abdullah S. (57211144258)
    ;
    Ukwaja, Kingsley (57202824584)
    ;
    Uthman, Olalekan A. (23026328100)
    ;
    Westerman, Ronny (57218361023)
    ;
    Wubshet, Mamo (54409732600)
    ;
    Yenesew, Muluken A. (39361108000)
    ;
    Yonemoto, Naohiro (57204947657)
    ;
    Younis, Mustafa Z. (8549393000)
    ;
    Zaidi, Zoubida (57197376721)
    ;
    El Sayed Zaki, Maysaa (57203666922)
    ;
    Al Rabeeah, Abdullah A. (6603625258)
    ;
    Wang, Haidong (16507828100)
    ;
    Naghavi, Mohsen (57207906323)
    ;
    Vos, Theo (57223885848)
    ;
    Lopez, Alan D. (7401455668)
    ;
    Murray, Christopher J. L. (55481130700)
    ;
    Mokdad, Ali H. (7004813962)
    Diarrheal diseases (DD) are leading causes of disease burden, death, and disability, especially in children in low-income settings. DD can also impact a child's potential livelihood through stunted physical growth, cognitive impairment, and other sequelae. As part of the Global Burden of Disease Study, we estimated DD burden, and the burden attributable to specific risk factors and particular etiologies, in the Eastern Mediterranean Region (EMR) between 1990 and 2013. For both sexes and all ages, we calculated disability-adjusted life years (DALYs), which are the sum of years of life lost and years lived with disability. We estimate that over 125,000 deaths (3.6% of total deaths) were due to DD in the EMR in 2013, with a greater burden of DD in low-and middle-income countries. Diarrhea deaths per 100,000 children under 5 years of age ranged from one (95% uncertainty interval [UI] = 0-1) in Bahrain and Oman to 471 (95% UI = 245-763) in Somalia. The pattern for diarrhea DALYs among those under 5 years of age closely followed that for diarrheal deaths. DALYs per 100,000 ranged from 739 (95% UI = 520-989) in Syria to 40,869 (95% UI = 21,540-65,823) in Somalia. Our results highlighted a highly inequitable burden of DD in EMR, mainly driven by the lack of access to proper resources such as water and sanitation. Our findings will guide preventive and treatment interventions which are based on evidence and which follow the ultimate goal of reducing the DD burden. Copyright © 2016 by The American Society of Tropical Medicine and Hygiene.
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    Publication
    Burden of obesity in the Eastern Mediterranean Region: findings from the Global Burden of Disease 2015 study
    (2018)
    Mokdad, Ali H (7004813962)
    ;
    El Bcheraoui, Charbel (25027689700)
    ;
    Afshin, Ashkan (57217465455)
    ;
    Charara, Raghid (56514085300)
    ;
    Khalil, Ibrahim (58255049500)
    ;
    Moradi-Lakeh, Maziar (35617421300)
    ;
    Kassebaum, Nicholas J (57202562224)
    ;
    Collison, Michael (57202309052)
    ;
    Daoud, Farah (57201079837)
    ;
    Krohn, Kristopher J (57194138806)
    ;
    Chew, Adrienne (57209171085)
    ;
    Biryukov, Stan H (57195296731)
    ;
    Cornaby, Leslie (57191837051)
    ;
    Foreman, Kyle J (57209064414)
    ;
    Kutz, Michael (57195617315)
    ;
    Liu, Patrick (56170368200)
    ;
    Reitsma, Marissa (57208766315)
    ;
    Sur, Patrick (57218360398)
    ;
    Wang, Haidong (16507828100)
    ;
    Zipkin, Ben (57200737130)
    ;
    Ärnlöv, Johan (6602512227)
    ;
    Abbafati, Cristiana (54917122400)
    ;
    Abdulle, Abdishakur M (6603592018)
    ;
    Abu-Rmeileh, Niveen M.E. (57216675148)
    ;
    Ahmed, Muktar Beshir (57207802317)
    ;
    Al-Aly, Ziyad (9738161500)
    ;
    Alam, Khurshid (57203681299)
    ;
    Alizadeh-Navaei, Reza (36024974700)
    ;
    Alkerwi, Ala'a (57197724313)
    ;
    Altirkawi, Khalid A (57202762923)
    ;
    Alvis-Guzman, Nelson (57210741239)
    ;
    Baune, Bernhard T (6603807336)
    ;
    Bedi, Neeraj (57988442200)
    ;
    Bennett, Derrick A (57650836400)
    ;
    Beyene, Addisu S (57209036705)
    ;
    Bhutta, Zulfiqar A (24342648300)
    ;
    Birhanu, Mulugeta M (57195446157)
    ;
    Danawi, Hadi (57201079895)
    ;
    Fereshtehnejad, Seyed-Mohammad (57202557520)
    ;
    Fischer, Florian (55508208800)
    ;
    Gebrehiwot, Tsegaye Tewelde (57216482917)
    ;
    Gill, Paramjit Singh (7202766660)
    ;
    Gona, Philimon N (57219703762)
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    Gupta, Vipin (57199940653)
    ;
    Habtewold, Tesfa Dejenie (57079013900)
    ;
    Hamadeh, Randah Ribhi (57202769526)
    ;
    Hamidi, Samer (24366336000)
    ;
    Hareri, Habtamu Abera (57195292447)
    ;
    Horino, Masako (57195769276)
    ;
    Hsairi, Mohamed (57209033943)
    ;
    Javanbakht, Mehdi (57204619886)
    ;
    John, Denny (57194230095)
    ;
    Jonas, Jost B (7202492953)
    ;
    Joshua, Vasna (57196474987)
    ;
    Kasaeian, Amir (57195540738)
    ;
    Ketema, Ezra B (56866354200)
    ;
    Khader, Yousef Saleh (55654192600)
    ;
    Khan, Ejaz Ahmad (57218791274)
    ;
    Khubchandani, Jagdish (57211720011)
    ;
    Kim, Daniel (57223019104)
    ;
    Kim, Yun Jin (57211086375)
    ;
    Kinfu, Yohannes (12770281900)
    ;
    Kokubo, Yoshihiro (56155004000)
    ;
    Larson, Heidi J (57202559142)
    ;
    Lee, Paul H (57200302692)
    ;
    Lunevicius, Raimundas (57216165063)
    ;
    Abd El Razek, Hassan Magdy (57195948985)
    ;
    Abd El Razek, Mohammed Magdy (57192379650)
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    Malekzadeh, Reza (7005197760)
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    Mate, Kedar K (57209031379)
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    Memish, Ziad A (7005059350)
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    Mengistie, Mubarek Abera (56045752700)
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    Mensah, George A (57196028147)
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    Ogbo, Felix Akpojene (57200737136)
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    Pourmalek, Farshad (8309390500)
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    Rafay, Anwar (57212263323)
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    Qorbani, Mostafa (24831040300)
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    Rahimi-Movaghar, Vafa (6507646446)
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    Rana, Saleem M (57204884092)
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    Rawaf, Salman (6602475959)
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    Renzaho, Andre M.N. (6505786588)
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    Rezaei, Satar (55791003000)
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    Rezai, Mohammad Sadegh (55273796300)
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    Safdarian, Mahdi (57203849024)
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    Sahraian, Mohammad Ali (55886074600)
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    Salamati, Payman (14045860600)
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    Samy, Abdallah M (36973661300)
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    Sanabria, Juan Ramon (7006262917)
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    Santric Milicevic, Milena M. (57211144346)
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    Sartorius, Benn (12788526800)
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    Sepanlou, Sadaf G (36248136000)
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    Shaikh, Masood Ali (57203122601)
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    Shiri, Rahman (57200737050)
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    Silva, Diego Augusto Santos (36985158000)
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    Singh, Jasvinder A (7404421736)
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    Terkawi, Abdullah Sulieman (57211144258)
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    Tiruye, Tenaw Yimer (57194055872)
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    Ukwaja, Kingsley Nnanna (57202824584)
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    Vasankari, Tommi (57200592416)
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    Vlassov, Vasiliy Victorovich (57211633239)
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    Wakayo, Tolassa (57205609717)
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    Werdecker, Andrea (57210505244)
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    Yonemoto, Naohiro (57204947657)
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    Younis, Mustafa Z (8549393000)
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    Zein, Bassel (57195293856)
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    Jumaan, Aisha O (6603612494)
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    Vos, Theo (57223885848)
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    Hay, Simon I (7101875313)
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    Naghavi, Mohsen (57207906323)
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    Murray, Christopher J.L. (55481130700)
    Objectives: We used the Global Burden of Disease (GBD) 2015 study results to explore the burden of high body mass index (BMI) in the Eastern Mediterranean Region (EMR). Methods: We estimated the prevalence of overweight and obesity among children (2–19 years) and adults (≥20 years) in 1980 and 2015. The burden of disease related to high BMI was calculated using the GBD comparative risk assessment approach. Results: The prevalence of obesity increased for adults from 15.1% (95% UI 13.4–16.9) in 1980 to 20.7% (95% UI 18.8–22.8) in 2015. It increased from 4.1% (95% UI 2.9–5.5) to 4.9% (95% UI 3.6–6.4) for the same period among children. In 2015, there were 417,115 deaths and 14,448,548 disability-adjusted life years (DALYs) attributable to high BMI in EMR, which constitute about 10 and 6.3% of total deaths and DALYs, respectively, for all ages. Conclusions: This is the first study to estimate trends in obesity burden for the EMR from 1980 to 2015. We call for EMR countries to invest more resources in prevention and health promotion efforts to reduce this burden. © 2017, The Author(s).
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    Causes of blindness and vision impairment in 2020 and trends over 30 years, and prevalence of avoidable blindness in relation to VISION 2020: The Right to Sight: An analysis for the Global Burden of Disease Study
    (2021)
    Steinmetz, Jaimie D. (57221591053)
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    Bourne, Rupert R.A. (7103377631)
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    Briant, Paul Svitil (57196152334)
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    Flaxman, Seth (35190257400)
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    Taylor, Hugh R. (55550572900)
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    Jonas, Jost B. (7202492953)
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    Abdoli, Amir (59421084100)
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    Abrha, Woldu Aberhe (57210943530)
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    Abualhasan, Ahmed (57211135523)
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    Abu-Gharbieh, Eman (24586714800)
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    Adal, Tadele Girum (57221588673)
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    Afshin, Ashkan (57217465455)
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    Ahmadieh, Hamid (57217239897)
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    Alemayehu, Wondu (6603772848)
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    Alemzadeh, Sayyed Amirpooya (56082872000)
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    Alfaar, Ahmed Samir (55319978300)
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    Alipour, Vahid (56436629300)
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    Androudi, Sofia (6603286512)
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    Arabloo, Jalal (57208760927)
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    Arditi, Aries (57207554001)
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    Aregawi, Brhane Berhe (57221588539)
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    Arrigo, Alessandro (56331647600)
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    Ashbaugh, Charlie (57218878439)
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    Ashrafi, Elham (35267734300)
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    Atnafu, Desta Debalkie (57203502301)
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    Bagli, Eleni (6506528499)
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    Baig, Atif Amin (49460999600)
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    Bärnighausen, Till Winfried (59454576800)
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    Parodi, Maurizio Battaglia (57218664419)
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    Beheshti, Mahya (57208333398)
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    Bhagavathula, Akshaya Srikanth (57217185969)
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    Bhardwaj, Nikha (57221591832)
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    Bhattacharyya, Krittika (57204647266)
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    Braithwaite, Tasanee (55522947000)
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    Bron, Alain M. (7103248039)
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    Nagaraja, Sharath Burugina (46961272800)
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    Butt, Zahid A. (57202522739)
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    Luciano Caetano dos Santos, Florentino (56373058500)
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    Carneiro, Vera L.A. (57213266524)
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    Casson, Robert James (6603840796)
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    Cheng, Ching-Yu (59286970100)
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    Choi, Jee-Young Jasmine (57209706428)
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    Chu, Dinh-Toi (56239816300)
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    Cicinelli, Maria Vittoria (37260895200)
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    Coelho, João M. (57194215965)
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    Congdon, Nathan G. (57217248626)
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    Couto, Rosa A.S. (56132363700)
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    Cromwell, Elizabeth A. (15727546000)
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    Dahlawi, Saad M.A. (57189234459)
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    Dai, Xiaochen (57221591169)
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    Dana, Reza (9436665700)
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    Dandona, Lalit (7007017243)
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    Del Monte, Monte A. (7005134758)
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    Desta, Abebaw Alemayehu (57224144903)
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    Ellwein, Leon B. (7004442455)
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    Golechha, Mahaveer (36006347600)
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    Hamidi, Samer (24366336000)
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    Hammond, Billy Randall (57527028300)
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    Hartnett, Mary Elizabeth R. (59578717600)
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    Hartono, Risky Kusuma (57217642211)
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    Hashi, Abdiwahab (57193562090)
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    Hay, Simon I. (7101875313)
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    Hayat, Khezar (57219918947)
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    Ho, Hung Chak (58753081000)
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    Holla, Ramesh (55270371800)
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    Househ, Mowafa (8667908000)
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    Huang, John J. (56135699200)
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    Ibitoye, Segun Emmanuel (57212027408)
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    Ilic, Irena M. (57210823522)
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    Ilic, Milena D. (7102981394)
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    Ingram, April D. (7005096948)
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    Irvani, Seyed Sina Naghibi (57202975543)
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    Islam, Sheikh Mohammed Shariful (57218355467)
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    Itumalla, Ramaiah (57212472658)
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    Jayaram, Shubha (57221589240)
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    Jha, Ravi Prakash (58586863400)
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    Kahloun, Rim (14119867400)
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    Kalhor, Rohollah (55670548600)
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    Kandel, Himal (57226834655)
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    Kasa, Ayele Semachew (57203538861)
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    Kavetskyy, Taras (57220358576)
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    Kayode, Gbenga A. (53463867400)
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    Kempen, John H. (57216598048)
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    Khairallah, Moncef (7004503022)
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    Khalilov, Rovshan (57193308858)
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    Khan, Ejaz Ahmad (59868841000)
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    Khanna, Rohit C. (14060213400)
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    Khatib, Mahalaqua Nazli (25825057100)
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    Khoja, Tawfik Ahmed Muthafer (7003561381)
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    Kim, Gyu Ri (58430876100)
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    Kim, Judy E. (15026687500)
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    Kim, Yun Jin (57211086375)
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    Kisa, Adnan (6603346067)
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    Kisa, Sezer (14030019900)
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    Kosen, Soewarta (57226828739)
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    Koyanagi, Ai (57197741912)
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    Bicer, Burcu Kucuk (57204528360)
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    Kulkarni, Vaman (56265708400)
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    Kurmi, Om P. (57219034567)
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    Landires, Iván (15063040000)
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    Lansingh, Van Charles (57209471470)
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    Leasher, Janet L. (57220556967)
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    LeGrand, Kate E. (57216789066)
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    Leveziel, Nicolas (35321211600)
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    Limburg, Hans (7003274856)
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    Liu, Xuefeng (37050047900)
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    Kunjathur, Shilpashree Madhava (56951087800)
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    Maleki, Shokofeh (57200675775)
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    Manafi, Navid (57190424904)
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    Mansouri, Kaweh (58294806200)
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    McAlinden, Colm (35325278500)
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    Meles, Gebrekiros Gebremichael (57211140536)
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    Mersha, Abera M. (57205064523)
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    Michalek, Irmina Maria (56982945900)
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    Miller, Ted R. (57226840428)
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    Misra, Sanjeev (35501005200)
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    Mohammad, Yousef (6603403710)
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    Mohammadi, Seyed Farzad (7005334788)
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    Mohammed, Jemal Abdu (57211142589)
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    Mokdad, Ali H. (59021699900)
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    Moni, Mohammad Ali (35119094400)
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    Al Montasir, Ahmed (57222707819)
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    Morse, Alan R. (7102718380)
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    Mulaw, Getahun Fentaw (57218820812)
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    Naderi, Mehdi (57202026927)
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    Naderifar, Homa (57188707273)
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    Naidoo, Kovin S. (35564549000)
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    Naimzada, Mukhammad David (57209744761)
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    Nangia, Vinay (57201490837)
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    Swamy, Sreenivas Narasimha (57222706843)
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    Naveed, Muhammad (58953995300)
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    Negash, Hadush (57209110507)
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    Nguyen, Huong Lan Thi (57226837406)
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    Nunez-Samudio, Virginia (15063201000)
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    Ogbo, Felix Akpojene (57217186813)
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    Ogundimu, Kolawole (6505646876)
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    Olagunju, Andrew T. (26029995700)
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    Onwujekwe, Obinna E. (7003992855)
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    Otstavnov, Nikita (57202947262)
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    Owolabi, Mayowa O. (59372043000)
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    Pakshir, Keyvan (15838075900)
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    Panda-Jonas, Songhomitra (6603112353)
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    Parekh, Utsav (55804990900)
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    Park, Eun-Cheol (57208356854)
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    Pasovic, Maja (57204523203)
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    Pawar, Shrikant (58594958600)
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    Pesudovs, Konrad (59156861800)
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    Peto, Tunde (7005772831)
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    Pham, Hai Quang (57217078995)
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    Pinheiro, Marina (54397531500)
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    Podder, Vivek (57201487580)
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    Rahimi-Movaghar, Vafa (6507646446)
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    Rahman, Mohammad Hifz Ur (57208867497)
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    Ramulu, Pradeep Y. (6602186935)
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    Rathi, Priya (57216633909)
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    Rawaf, David Laith (57209228052)
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    Rawaf, Salman (6602475959)
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    Rawal, Lal (37262106500)
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    Reinig, Nickolas (57208577401)
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    Renzaho, Andre M.N. (57217062482)
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    Rezapour, Aziz (55548281300)
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    Robin, Alan L. (35373759700)
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    Rossetti, Luca (57078136300)
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    Sabour, Siamak (16307842100)
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    Safi, Sare (57219477293)
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    Sahebkar, Amirhossein (26639699900)
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    Sahraian, Mohammad Ali (57219968932)
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    Samy, Abdallah M. (36973661300)
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    Sathian, Brijesh (27467953500)
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    Saya, Ganesh Kumar (55391007900)
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    Saylan, Mete (56253241700)
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    Shaheen, Amira A. (57202954176)
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    Shaikh, Masood Ali (56673685600)
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    Shen, Tueng T. (36852423700)
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    Shibuya, Kenji (8948057900)
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    Shiferaw, Wondimeneh Shibabaw (57214329180)
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    Shigematsu, Mika (23968093000)
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    Shin, Jae Il (59734917100)
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    Silva, Juan Carlos (8576007400)
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    Silvester, Alexander (33068382100)
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    Singh, Jasvinder A. (58179112300)
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    Singhal, Deepika (48361953900)
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    Sitorus, Rita S. (57221587271)
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    Skiadaresi, Eirini (37100428500)
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    Skryabin, Valentin Yurievich (57226830981)
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    Skryabina, Anna Aleksandrovna (57218875198)
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    Soheili, Amin (57204123755)
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    Sorrie, Muluken Bekele (57195303874)
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    Sousa, Raúl A.R.C. (57218215064)
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    Sreeramareddy, Chandrashekhar T. (57212263335)
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    Stambolian, Dwight (58141205300)
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    Tadesse, Eyayou Girma (57221591705)
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    Tahhan, Nina (6507557960)
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    Tareque, Md Ismail (58298394400)
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    Topouzis, Fotis (57194262710)
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    Tran, Bach Xuan (57209107515)
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    Tsegaye, Gebiyaw Wudie (57216732977)
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    Tsilimbaris, Miltiadis K. (57216802043)
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    Varma, Rohit (57218390144)
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    Virgili, Gianni (7006732630)
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    Vongpradith, Avina (57216661011)
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    Vu, Giang Thu (57226824976)
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    Wang, Ya Xing (47962560100)
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    Wang, Ningli (59683171300)
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    Weldemariam, Abrha Hailay (57221587797)
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    West, Sheila K. (59297599300)
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    Wondmeneh, Temesgen Gebeyehu (57219426999)
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    Wong, Tien Y. (59437790500)
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    Yaseri, Mehdi (23029507000)
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    Yonemoto, Naohiro (59681251600)
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    Yu, Chuanhua (57208140344)
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    Zastrozhin, Mikhail Sergeevich (56728932200)
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    Zastrozhina, Anasthasia (57210832491)
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    Zhang, Zhi-Jiang (56068578400)
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    Zimsen, Stephanie R.M. (57196078433)
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    Resnikoff, Serge (7006012071)
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    Vos, Theo (57223885848)
    Background: Many causes of vision impairment can be prevented or treated. With an ageing global population, the demands for eye health services are increasing. We estimated the prevalence and relative contribution of avoidable causes of blindness and vision impairment globally from 1990 to 2020. We aimed to compare the results with the World Health Assembly Global Action Plan (WHA GAP) target of a 25% global reduction from 2010 to 2019 in avoidable vision impairment, defined as cataract and undercorrected refractive error. Methods: We did a systematic review and meta-analysis of population-based surveys of eye disease from January, 1980, to October, 2018. We fitted hierarchical models to estimate prevalence (with 95% uncertainty intervals [UIs]) of moderate and severe vision impairment (MSVI; presenting visual acuity from <6/18 to 3/60) and blindness (<3/60 or less than 10° visual field around central fixation) by cause, age, region, and year. Because of data sparsity at younger ages, our analysis focused on adults aged 50 years and older. Findings: Global crude prevalence of avoidable vision impairment and blindness in adults aged 50 years and older did not change between 2010 and 2019 (percentage change −0·2% [95% UI −1·5 to 1·0]; 2019 prevalence 9·58 cases per 1000 people [95% IU 8·51 to 10·8], 2010 prevalence 96·0 cases per 1000 people [86·0 to 107·0]). Age-standardised prevalence of avoidable blindness decreased by −15·4% [–16·8 to −14·3], while avoidable MSVI showed no change (0·5% [–0·8 to 1·6]). However, the number of cases increased for both avoidable blindness (10·8% [8·9 to 12·4]) and MSVI (31·5% [30·0 to 33·1]). The leading global causes of blindness in those aged 50 years and older in 2020 were cataract (15·2 million cases [9% IU 12·7–18·0]), followed by glaucoma (3·6 million cases [2·8–4·4]), undercorrected refractive error (2·3 million cases [1·8–2·8]), age-related macular degeneration (1·8 million cases [1·3–2·4]), and diabetic retinopathy (0·86 million cases [0·59–1·23]). Leading causes of MSVI were undercorrected refractive error (86·1 million cases [74·2–101·0]) and cataract (78·8 million cases [67·2–91·4]). Interpretation: Results suggest eye care services contributed to the observed reduction of age-standardised rates of avoidable blindness but not of MSVI, and that the target in an ageing global population was not reached. Funding: Brien Holden Vision Institute, Fondation Théa, The Fred Hollows Foundation, Bill & Melinda Gates Foundation, Lions Clubs International Foundation, Sightsavers International, and University of Heidelberg. © 2021 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
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    Erratum: Global, regional, and national age-sex-specific mortality for 282 causes of death in 195 countries and territories, 1980–2017: a systematic analysis for the Global Burden of Disease Study 2017 (The Lancet (2018) 392(10159) (1736–1788)(S0140673618322037)(10.1016/S0140-6736(18)32203-7))
    (2018)
    Roth, Gregory A. (55074747400)
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    Abate, Degu (57204237665)
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    Abate, Kalkidan Hassen (57207943858)
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    Abay, Solomon M. (35306466900)
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    Abbafati, Cristiana (54917122400)
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    Abbasi, Nooshin (57212442022)
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    Abbastabar, Hedayat (57212441848)
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    Abd-Allah, Foad (36503428900)
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    Abdela, Jemal (57200613000)
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    Abdelalim, Ahmed (7801307783)
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    Abdollahpour, Ibrahim (36997151900)
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    Abdulkader, Rizwan Suliankatchi (57195295816)
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    Abebe, Haftom Temesgen (55950002100)
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    Abebe, Molla (57211131124)
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    Abebe, Zegeye (57193002719)
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    Abejie, Ayenew Negesse (57203015573)
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    Abera, Semaw F. (57205180598)
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    Abil, Olifan Zewdie (57204558002)
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    Abraha, Haftom Niguse (57195289877)
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    Abrham, Aklilu Roba (57202704637)
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    Abu-Raddad, Laith Jamal (14032724700)
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    Accrombessi, Manfred Mario Kokou (55353650500)
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    Acharya, Dilaram (56770895600)
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    Adamu, Abdu A. (57202024381)
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    Adebayo, Oladimeji M. (57194329853)
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    Adedoyin, Rufus Adesoji (55947572800)
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    Adekanmbi, Victor (53463192900)
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    Adetokunboh, Olatunji O. (56598104300)
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    Adhena, Beyene Meressa (57322512000)
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    Adib, Mina G. (57204560513)
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    Admasie, Amha (56609274200)
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    Afshin, Ashkan (57217465455)
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    Agarwal, Gina (57220151944)
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    Agesa, Kareha M. (57204562362)
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    Agrawal, Anurag (35214460700)
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    Agrawal, Sutapa (57202841733)
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    Ahmadi, Alireza (56336080700)
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    Ahmadi, Mehdi (16644923000)
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    Ahmed, Muktar Beshir (57207802317)
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    Ahmed, Sayem (58601030100)
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    Aichour, Amani Nidhal (57195486768)
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    Aichour, Ibtihel (57195485980)
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    Aichour, Miloud Taki Eddine (57195488258)
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    Akbari, Mohammad Esmaeil (56666938200)
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    Akinyemi, Rufus Olusola (25633566800)
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    Akseer, Nadia (57207801968)
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    Al-Aly, Ziyad (9738161500)
    ;
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    GBD 2017 Causes of Death Collaborators. Global, regional, and national age-sex-specific mortality for 282 causes of death in 195 countries and territories, 1980–2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet 2018; 392: 1736–88—The bottom row in figure 7 was cut off. This correction has been made to the online version as of Nov 9, 2018, and has been made to the printed Article. © 2018 Elsevier Ltd
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    Erratum: Global, regional, and national comparative risk assessment of 84 behavioural, environmental and occupational, and metabolic risks or clusters of risks for 195 countries and territories, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017 (The Lancet (2018) 392(10159) (1923–1994), (S0140673618322256), (10.1016/S0140-6736(18)32225-6))
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    Mousavi, Seyyed Meysam (56165159700)
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    Mozaffarian, Dariush (56751007100)
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    Mruts, Kalayu Brhane (57221822877)
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    Muche, Achenef Asmamaw (57195576373)
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    Muchie, Kindie Fentahun (57194458469)
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    Mueller, Ulrich Otto (8512347500)
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    Muhammed, Oumer Sada (57202727745)
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    Mukhopadhyay, Satinath (36342847700)
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    Muller, Kate (57196075658)
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    Musa, Kamarul Imran (57194536466)
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    Mustafa, Ghulam (57190395960)
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    Nabhan, Ashraf F. (55880870200)
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    Naghavi, Mohsen (57207906323)
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    Naheed, Aliya (57202560989)
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    Nahvijou, Azin (18837247000)
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    Naik, Gurudatta (56020694000)
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    Naik, Nitish (7006558334)
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    Najafi, Farid (21743304900)
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    Nangia, Vinay (57201490837)
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    Nansseu, Jobert Richie (55548984700)
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    Nascimento, Bruno Ramos (14424406800)
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    Neal, Bruce (57218390053)
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    Neamati, Nahid (57204566952)
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    Negoi, Ionut (57200640014)
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    Negoi, Ruxandra Irina (55566106200)
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    Neupane, Subas (57215632313)
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    Newton, Charles Richard James (35465836500)
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    Ngunjiri, Josephine W. (57195296110)
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    Nguyen, Anh Quynh (57204557413)
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    Nguyen, Grant (57191591002)
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    Nguyen, Ha Thu (57468278900)
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    Nguyen, Huong Lan Thi (57226837406)
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    Nguyen, Huong Thanh (37093238600)
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    Nguyen, Minh (58203329200)
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    Nguyen, Nam Ba (57204561572)
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    Nichols, Emma (57205756163)
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    Nie, Jing (57191615022)
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    Ningrum, Dina Nur Anggraini (57195329470)
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    Nirayo, Yirga Legesse (57201651103)
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    Nishi, Nobuo (7103131706)
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    Nixon, Molly R. (57204562047)
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    Nojomi, Marzieh (22941666400)
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    Nomura, Shuhei (55632290700)
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    Norheim, Ole F. (7004082597)
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    Nouri, Hamid Reza (57202484612)
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    Nourollahpour Shiadeh, Malihe (56960536000)
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    Nowroozi, Mohammad Reza (8866311900)
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    Nsoesie, Elaine O. (57211006304)
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    Nyasulu, Peter S. (36700333500)
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    Obermeyer, Carla M. (57209300189)
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    Odell, Christopher M. (57204283884)
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    Ofori-Asenso, Richard (57209300265)
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    Ogbo, Felix Akpojene (57217186813)
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    Oh, In-Hwan (57204090669)
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    Oladimeji, Olanrewaju (57216495380)
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    Olagunju, Andrew T. (26029995700)
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    Olagunju, Tinuke O. (57203076824)
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    Olivares, Pedro R. (7003510190)
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    Olsen, Helen Elizabeth (57203080494)
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    Olusanya, Bolajoko Olubukunola (57218504682)
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    Olusanya, Jacob Olusegun (57222488860)
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    Ong, Kanyin L. (57210793447)
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    Ong, Sok King (36614524300)
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    Oren, Eyal (36815569400)
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    Orpana, Heather M. (6507559930)
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    Ortiz, Alberto (7201911399)
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    Ota, Erika (57202554474)
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    Otstavnov, Stanislav S. (57204561394)
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    Øverland, Simon (23028540300)
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    Owolabi, Mayowa Ojo (57222581892)
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    Mahesh, P.A. (57202421244)
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    Pacella, Rosana (57194839077)
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    Pakhare, Abhijit P. (54383993100)
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    Pakpour, Amir H. (56181056500)
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    Pana, Adrian (57191837583)
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    Panda-Jonas, Songhomitra (6603112353)
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    Park, Eun-Kee (57216814178)
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    Parry, Charles D.H. (7102561312)
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    Parsian, Hadi (55991107900)
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    Patel, Shanti (57072227700)
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    Pati, Sanghamitra (55441302100)
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    Patil, Snehal T. (57212263349)
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    Patle, Ajay (57203309187)
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    Patton, George C. (7102184358)
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    Paudel, Deepak (57207871851)
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    Paulson, Katherine R. (57203437789)
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    Paz Ballesteros, Wayra Citlali (57194434337)
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    Pearce, Neil (56491440700)
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    Pereira, Alexandre (7402230187)
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    Pereira, David M. (57200690024)
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    Perico, Norberto (56481931200)
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    Petzold, Max (7003628893)
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    Pham, Hai Quang (57217078995)
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    Phillips, Michael R. (57206972395)
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    Pillay, Julian David (57197803061)
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    Piradov, Michael A. (7003731802)
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    Plana-Ripoll, Oleguer (41662092800)
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    Polkinghorne, Kevan R. (6601997825)
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    Postma, Maarten J. (7006296502)
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    Pourshams, Akram (6507521541)
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    Purcell, Caroline A. (56203575500)
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    Purwar, Manorama B. (6602127625)
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    Qorbani, Mostafa (24831040300)
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    Radfar, Amir (57194428768)
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    Ram, Usha (26653819000)
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    Rawaf, David Laith (57209228052)
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    Reddy, K. Srinath (35417788900)
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    Rehm, Colin D. (23478097800)
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    Rehm, Jürgen (7102718648)
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    Reiner, Robert C. (57203229088)
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    Reitsma, Marissa B. (57208766315)
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    Remuzzi, Giuseppe (56466188600)
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    Renzaho, Andre M.N. (6505786588)
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    Resnikoff, Serge (7006012071)
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    Reynales-Shigematsu, Luz Myriam (12142340100)
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    Rezaei, Satar (55791003000)
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    Ribeiro, Antonio Luiz P. (7201676223)
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    Rivera, Juan A. (7202308740)
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    Rodríguez-Ramírez, Sonia (25229455200)
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    Roever, Leonardo (56641632800)
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    Ronfani, Luca (6602565620)
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    Roshandel, Gholamreza (14034446800)
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    Rostami, Ali (7005439033)
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    Roth, Gregory A. (55074747400)
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    Rothenbacher, Dietrich (7004765162)
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    Roy, Ambuj (7402704658)
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    Rubagotti, Enrico (57208389589)
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    Rushton, Lesley (57202561819)
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    Sabanayagam, Charumathi (22136294700)
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    Sachdev, Perminder S. (7102284091)
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    Salz, Inbal (57199623777)
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    Samy, Abdallah M. (36973661300)
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    Sánchez-Pimienta, Tania G. (57042673800)
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    Sanders, Taren (55369008700)
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    Sang, Yingying (55192664300)
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    Santomauro, Damian Francesco (56912450700)
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    Santos, Itamar S. (57198312911)
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    Santos, João Vasco (57226214352)
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    Santric Milicevic, Milena M. (57211144346)
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    Sao Jose, Bruno Piassi (57204561719)
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    Sardana, Mayank (56992882500)
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    Sarrafzadegan, Nizal (6701751316)
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    Sartorius, Benn (12788526800)
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    Schaeffner, Elke (6507021741)
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    Schmidt, Maria Inês (7404398885)
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    Schöttker, Ben (37665918200)
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    Sepanlou, Sadaf G. (36248136000)
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    Serre, Marc L. (7003717099)
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    Serván-Mori, Edson (57202594826)
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    Seyedmousavi, Seyedmojtaba (57204698893)
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    Shaheen, Amira A. (57202560956)
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    Shaikh, Masood Ali (57203122601)
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    Shamah Levy, Teresa (57215134479)
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    Sharif-Alhoseini, Mahdi (35108018000)
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    Sharifi, Hamid (16643763200)
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    Sharma, Jayendra (57195329457)
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    Sharma, Meenakshi (58730797800)
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    Sharma, Rajesh (58228412600)
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    She, Jun (57209122131)
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    Sheikh, Aziz (7202522962)
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    Shi, Peilin (57203064901)
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    Shibuya, Kenji (8948057900)
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    Shiferaw, Mekonnen Sisay (57205232012)
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    Shigematsu, Mika (23968093000)
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    Shin, Min-Jeong (7401536640)
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    Shiri, Rahman (57200737050)
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    Shirkoohi, Reza (12776374400)
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    Shiue, Ivy (35811219800)
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    Shokraneh, Farhad (36146063000)
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    Shoman, Haitham (57208324664)
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    Shrime, Mark G. (57204703404)
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    Shupler, Matthew S. (57191750323)
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    Si, Si (56706979500)
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    Siabani, Soraya (25227131300)
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    Sibai, Abla Mehio (7005466998)
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    Siddiqi, Tariq J. (57193718539)
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    Sigfusdottir, Inga Dora (57214359118)
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    Sigurvinsdottir, Rannveig (56006396200)
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    Silva, Diego Augusto Santos (36985158000)
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    Silva, João Pedro (57204703526)
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    Silveira, Dayane Gabriele Alves (57190284103)
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    Singh, Jasvinder A. (7404421736)
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    Singh, Narinder Pal (57211864736)
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    Singh, Virendra (57191848598)
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    Sinha, Dhirendra Narain (7201637609)
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    Skiadaresi, Eirini (37100428500)
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    Skirbekk, Vegard (57202564482)
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    Smith, David L. (55574206203)
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    Smith, Mari (57195484737)
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    Sobaih, Badr Hasan (57202564080)
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    Sobhani, Soheila (57193095221)
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    Somayaji, Ranjani (6507727557)
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    Soofi, Moslem (56373891000)
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    Sorensen, Reed J.D. (57196918748)
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    Soriano, Joan B. (7101973935)
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    Soyiri, Ireneous N. (15052406400)
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    Spinelli, Angela (7102473362)
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    Sposato, Luciano A. (25640261000)
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    Sreeramareddy, Chandrashekhar T. (57212263335)
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    Srinivasan, Vinay (57196077031)
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    Starodubov, Vladimir I. (6701820838)
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    Steckling, Nadine (57199195462)
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    Stein, Dan J. (55769747595)
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    Stein, Murray B. (7402996817)
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    Stevanovic, Goran (15059280200)
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    Stockfelt, Leo (26022098300)
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    Stokes, Mark A. (7102859000)
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    Sturua, Lela (37662283900)
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    Subart, Michelle L. (57194140438)
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    Sudaryanto, Agus (57305372500)
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    Sufiyan, Mu’awiyyah Babale (58294633600)
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    Sulo, Gerhard (16242476100)
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    Sunguya, Bruno F. (57209060557)
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    Sur, Patrick John (57218360398)
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    Sykes, Bryan L. (57218362022)
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    Szoeke, Cassandra E.I. (6505920990)
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    Tabarés-Seisdedos, Rafael (6602981102)
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    Tabuchi, Takahiro (55177892400)
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    Tadakamadla, Santosh Kumar (57207799926)
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    Takahashi, Ken (55741242600)
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    Tandon, Nikhil (7101833756)
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    Tassew, Segen Gebremeskel (57204569108)
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    Tavakkoli, Mohammad (57202524239)
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    Taveira, Nuno (6602731390)
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    Tehrani-Banihashemi, Arash (57204006020)
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    Tekalign, Tigist Gashaw (57204558037)
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    Tekelemedhin, Shishay Wahdey (57204566273)
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    Tekle, Merhawi Gebremedhin (57204237146)
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    Temesgen, Habtamu (57205011874)
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    Temsah, Mohamad-Hani (56115852000)
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    Temsah, Omar (57204559820)
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    Terkawi, Abdullah Sulieman (57211144258)
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    Tessema, Belay (20735503600)
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    Teweldemedhin, Mebrahtu (57193667629)
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    Thankappan, Kavumpurathu Raman (57202955435)
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    Theis, Andrew (57196076787)
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    Thirunavukkarasu, Sathish (54407369300)
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    Thomas, Hannah J. (55925904000)
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    Thomas, Matthew Lloyd (57191835351)
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    Thomas, Nihal (7401830494)
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    Thurston, George D. (7102270013)
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    Tilahun, Binyam (57212075730)
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    Tillmann, Taavi (57190211142)
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    To, Quyen G. (55827789100)
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    Tobollik, Myriam (56549045300)
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    Tonelli, Marcello (7103102534)
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    Topor-Madry, Roman (57211182892)
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    Torre, Anna E. (57196074351)
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    Tortajada-Girbés, Miguel (16242320900)
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    Touvier, Mathilde (8877033300)
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    Tovani-Palone, Marcos Roberto (56644977900)
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    Towbin, Jeffrey A. (7102520568)
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    Tran, Bach Xuan (57209107515)
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    Tran, Khanh Bao (57201651536)
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    Truelsen, Thomas Clement (57202824565)
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    Truong, Nu Thi (57204178907)
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    Tsadik, Afewerki Gebremeskel (57204562442)
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    Tudor Car, Lorainne (48561867100)
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    Tuzcu, E. Murat (7005951350)
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    Tymeson, Hayley D. (57194139009)
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    Tyrovolas, Stefanos (57207793475)
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    Ukwaja, Kingsley N. (57202824584)
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    Ullah, Irfan (56992676600)
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    Updike, Rachel L. (57204698680)
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    Usman, Muhammad Shariq (57203046075)
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    Uthman, Olalekan A. (23026328100)
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    Vaduganathan, Muthiah (16417973600)
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    Vaezi, Afsane (55698015300)
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    Valdez, Pascual R. (57202115577)
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    Van Donkelaar, Aaron (15926418500)
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    Varavikova, Elena (7801408611)
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    Varughese, Santosh (22942817500)
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    Vasankari, Tommi Juhani (23096834700)
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    Venkateswaran, Vidhya (59829999400)
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    Venketasubramanian, Narayanaswamy (56804702100)
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    Villafaina, Santos (57195804127)
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    Violante, Francesco S. (7003555890)
    Background The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2017 comparative risk assessment (CRA) is a comprehensive approach to risk factor quantification that offers a useful tool for synthesising evidence on risks and risk–outcome associations. With each annual GBD study, we update the GBD CRA to incorporate improved methods, new risks and risk–outcome pairs, and new data on risk exposure levels and risk–outcome associations. Methods We used the CRA framework developed for previous iterations of GBD to estimate levels and trends in exposure, attributable deaths, and attributable disability-adjusted life-years (DALYs), by age group, sex, year, and location for 84 behavioural, environmental and occupational, and metabolic risks or groups of risks from 1990 to 2017. This study included 476 risk–outcome pairs that met the GBD study criteria for convincing or probable evidence of causation. We extracted relative risk and exposure estimates from 46 749 randomised controlled trials, cohort studies, household surveys, census data, satellite data, and other sources. We used statistical models to pool data, adjust for bias, and incorporate covariates. Using the counterfactual scenario of theoretical minimum risk exposure level (TMREL), we estimated the portion of deaths and DALYs that could be attributed to a given risk. We explored the relationship between development and risk exposure by modelling the relationship between the Socio-demographic Index (SDI) and risk-weighted exposure prevalence and estimated expected levels of exposure and risk-attributable burden by SDI. Finally, we explored temporal changes in risk-attributable DALYs by decomposing those changes into six main component drivers of change as follows: (1) population growth; (2) changes in population age structures; (3) changes in exposure to environmental and occupational risks; (4) changes in exposure to behavioural risks; (5) changes in exposure to metabolic risks; and (6) changes due to all other factors, approximated as the risk-deleted death and DALY rates, where the risk-deleted rate is the rate that would be observed had we reduced the exposure levels to the TMREL for all risk factors included in GBD 2017. Findings In 2017, 34·1 million (95% uncertainty interval [UI] 33·3–35·0) deaths and 1·21 billion (1·14–1·28) DALYs were attributable to GBD risk factors. Globally, 61·0% (59·6–62·4) of deaths and 48·3% (46·3–50·2) of DALYs were attributed to the GBD 2017 risk factors. When ranked by risk-attributable DALYs, high systolic blood pressure (SBP) was the leading risk factor, accounting for 10·4 million (9·39–11·5) deaths and 218 million (198–237) DALYs, followed by smoking (7·10 million [6·83–7·37] deaths and 182 million [173–193] DALYs), high fasting plasma glucose (6·53 million [5·23–8·23] deaths and 171 million [144–201] DALYs), high body-mass index (BMI; 4·72 million [2·99–6·70] deaths and 148 million [98·6–202] DALYs), and short gestation for birthweight (1·43 million [1·36–1·51] deaths and 139 million [131–147] DALYs). In total, risk-attributable DALYs declined by 4·9% (3·3–6·5) between 2007 and 2017. In the absence of demographic changes (ie, population growth and ageing), changes in risk exposure and risk-deleted DALYs would have led to a 23·5% decline in DALYs during that period. Conversely, in the absence of changes in risk exposure and risk-deleted DALYs, demographic changes would have led to an 18·6% increase in DALYs during that period. The ratios of observed risk exposure levels to exposure levels expected based on SDI (O/E ratios) increased globally for unsafe drinking water and household air pollution between 1990 and 2017. This result suggests that development is occurring more rapidly than are changes in the underlying risk structure in a population. Conversely, nearly universal declines in O/E ratios for smoking and alcohol use indicate that, for a given SDI, exposure to these risks is declining. In 2017, the leading Level 4 risk factor for age-standardised DALY rates was high SBP in four super-regions: central Europe, eastern Europe, and central Asia; north Africa and Middle East; south Asia; and southeast Asia, east Asia, and Oceania. The leading risk factor in the high-income super-region was smoking, in Latin America and Caribbean was high BMI, and in sub-Saharan Africa was unsafe sex. O/E ratios for unsafe sex in sub-Saharan Africa were notably high, and those for alcohol use in north Africa and the Middle East were notably low. Interpretation By quantifying levels and trends in exposures to risk factors and the resulting disease burden, this assessment offers insight into where past policy and programme efforts might have been successful and highlights current priorities for public health action. Decreases in behavioural, environmental, and occupational risks have largely offset the effects of population growth and ageing, in relation to trends in absolute burden. Conversely, the combination of increasing metabolic risks and population ageing will probably continue to drive the increasing trends in non-communicable diseases at the global level, which presents both a public health challenge and opportunity. We see considerable spatiotemporal heterogeneity in levels of risk exposure and risk-attributable burden. Although levels of development underlie some of this heterogeneity, O/E ratios show risks for which countries are overperforming or underperforming relative to their level of development. As such, these ratios provide a benchmarking tool to help to focus local decision making. Our findings reinforce the importance of both risk exposure monitoring and epidemiological research to assess causal connections between risks and health outcomes, and they highlight the usefulness of the GBD study in synthesising data to draw comprehensive and robust conclusions that help to inform good policy and strategic health planning. Copyright © 2018 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license.
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    Global burden and strength of evidence for 88 risk factors in 204 countries and 811 subnational locations, 1990–2021: a systematic analysis for the Global Burden of Disease Study 2021
    (2024)
    Brauer, Michael (57218330976)
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    Roth, Gregory A. (58876328900)
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    Maled, Venkatesh (59317098500)
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    Malik, Ahmad Azam (57198682313)
    Background: Understanding the health consequences associated with exposure to risk factors is necessary to inform public health policy and practice. To systematically quantify the contributions of risk factor exposures to specific health outcomes, the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2021 aims to provide comprehensive estimates of exposure levels, relative health risks, and attributable burden of disease for 88 risk factors in 204 countries and territories and 811 subnational locations, from 1990 to 2021. Methods: The GBD 2021 risk factor analysis used data from 54 561 total distinct sources to produce epidemiological estimates for 88 risk factors and their associated health outcomes for a total of 631 risk–outcome pairs. Pairs were included on the basis of data-driven determination of a risk–outcome association. Age-sex-location-year-specific estimates were generated at global, regional, and national levels. Our approach followed the comparative risk assessment framework predicated on a causal web of hierarchically organised, potentially combinative, modifiable risks. Relative risks (RRs) of a given outcome occurring as a function of risk factor exposure were estimated separately for each risk–outcome pair, and summary exposure values (SEVs), representing risk-weighted exposure prevalence, and theoretical minimum risk exposure levels (TMRELs) were estimated for each risk factor. These estimates were used to calculate the population attributable fraction (PAF; ie, the proportional change in health risk that would occur if exposure to a risk factor were reduced to the TMREL). The product of PAFs and disease burden associated with a given outcome, measured in disability-adjusted life-years (DALYs), yielded measures of attributable burden (ie, the proportion of total disease burden attributable to a particular risk factor or combination of risk factors). Adjustments for mediation were applied to account for relationships involving risk factors that act indirectly on outcomes via intermediate risks. Attributable burden estimates were stratified by Socio-demographic Index (SDI) quintile and presented as counts, age-standardised rates, and rankings. To complement estimates of RR and attributable burden, newly developed burden of proof risk function (BPRF) methods were applied to yield supplementary, conservative interpretations of risk–outcome associations based on the consistency of underlying evidence, accounting for unexplained heterogeneity between input data from different studies. Estimates reported represent the mean value across 500 draws from the estimate's distribution, with 95% uncertainty intervals (UIs) calculated as the 2·5th and 97·5th percentile values across the draws. Findings: Among the specific risk factors analysed for this study, particulate matter air pollution was the leading contributor to the global disease burden in 2021, contributing 8·0% (95% UI 6·7–9·4) of total DALYs, followed by high systolic blood pressure (SBP; 7·8% [6·4–9·2]), smoking (5·7% [4·7–6·8]), low birthweight and short gestation (5·6% [4·8–6·3]), and high fasting plasma glucose (FPG; 5·4% [4·8–6·0]). For younger demographics (ie, those aged 0–4 years and 5–14 years), risks such as low birthweight and short gestation and unsafe water, sanitation, and handwashing (WaSH) were among the leading risk factors, while for older age groups, metabolic risks such as high SBP, high body-mass index (BMI), high FPG, and high LDL cholesterol had a greater impact. From 2000 to 2021, there was an observable shift in global health challenges, marked by a decline in the number of all-age DALYs broadly attributable to behavioural risks (decrease of 20·7% [13·9–27·7]) and environmental and occupational risks (decrease of 22·0% [15·5–28·8]), coupled with a 49·4% (42·3–56·9) increase in DALYs attributable to metabolic risks, all reflecting ageing populations and changing lifestyles on a global scale. Age-standardised global DALY rates attributable to high BMI and high FPG rose considerably (15·7% [9·9–21·7] for high BMI and 7·9% [3·3–12·9] for high FPG) over this period, with exposure to these risks increasing annually at rates of 1·8% (1·6–1·9) for high BMI and 1·3% (1·1–1·5) for high FPG. By contrast, the global risk-attributable burden and exposure to many other risk factors declined, notably for risks such as child growth failure and unsafe water source, with age-standardised attributable DALYs decreasing by 71·5% (64·4–78·8) for child growth failure and 66·3% (60·2–72·0) for unsafe water source. We separated risk factors into three groups according to trajectory over time: those with a decreasing attributable burden, due largely to declining risk exposure (eg, diet high in trans-fat and household air pollution) but also to proportionally smaller child and youth populations (eg, child and maternal malnutrition); those for which the burden increased moderately in spite of declining risk exposure, due largely to population ageing (eg, smoking); and those for which the burden increased considerably due to both increasing risk exposure and population ageing (eg, ambient particulate matter air pollution, high BMI, high FPG, and high SBP). Interpretation: Substantial progress has been made in reducing the global disease burden attributable to a range of risk factors, particularly those related to maternal and child health, WaSH, and household air pollution. Maintaining efforts to minimise the impact of these risk factors, especially in low SDI locations, is necessary to sustain progress. Successes in moderating the smoking-related burden by reducing risk exposure highlight the need to advance policies that reduce exposure to other leading risk factors such as ambient particulate matter air pollution and high SBP. Troubling increases in high FPG, high BMI, and other risk factors related to obesity and metabolic syndrome indicate an urgent need to identify and implement interventions. Funding: Bill & Melinda Gates Foundation. © 2024 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
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    Global burden of 369 diseases and injuries in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019
    (2020)
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    Mohammad, Yousef (6603403710)
    Background: In an era of shifting global agendas and expanded emphasis on non-communicable diseases and injuries along with communicable diseases, sound evidence on trends by cause at the national level is essential. The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) provides a systematic scientific assessment of published, publicly available, and contributed data on incidence, prevalence, and mortality for a mutually exclusive and collectively exhaustive list of diseases and injuries. Methods: GBD estimates incidence, prevalence, mortality, years of life lost (YLLs), years lived with disability (YLDs), and disability-adjusted life-years (DALYs) due to 369 diseases and injuries, for two sexes, and for 204 countries and territories. Input data were extracted from censuses, household surveys, civil registration and vital statistics, disease registries, health service use, air pollution monitors, satellite imaging, disease notifications, and other sources. Cause-specific death rates and cause fractions were calculated using the Cause of Death Ensemble model and spatiotemporal Gaussian process regression. Cause-specific deaths were adjusted to match the total all-cause deaths calculated as part of the GBD population, fertility, and mortality estimates. Deaths were multiplied by standard life expectancy at each age to calculate YLLs. A Bayesian meta-regression modelling tool, DisMod-MR 2.1, was used to ensure consistency between incidence, prevalence, remission, excess mortality, and cause-specific mortality for most causes. Prevalence estimates were multiplied by disability weights for mutually exclusive sequelae of diseases and injuries to calculate YLDs. We considered results in the context of the Socio-demographic Index (SDI), a composite indicator of income per capita, years of schooling, and fertility rate in females younger than 25 years. Uncertainty intervals (UIs) were generated for every metric using the 25th and 975th ordered 1000 draw values of the posterior distribution. Findings: Global health has steadily improved over the past 30 years as measured by age-standardised DALY rates. After taking into account population growth and ageing, the absolute number of DALYs has remained stable. Since 2010, the pace of decline in global age-standardised DALY rates has accelerated in age groups younger than 50 years compared with the 1990–2010 time period, with the greatest annualised rate of decline occurring in the 0–9-year age group. Six infectious diseases were among the top ten causes of DALYs in children younger than 10 years in 2019: lower respiratory infections (ranked second), diarrhoeal diseases (third), malaria (fifth), meningitis (sixth), whooping cough (ninth), and sexually transmitted infections (which, in this age group, is fully accounted for by congenital syphilis; ranked tenth). In adolescents aged 10–24 years, three injury causes were among the top causes of DALYs: road injuries (ranked first), self-harm (third), and interpersonal violence (fifth). Five of the causes that were in the top ten for ages 10–24 years were also in the top ten in the 25–49-year age group: road injuries (ranked first), HIV/AIDS (second), low back pain (fourth), headache disorders (fifth), and depressive disorders (sixth). In 2019, ischaemic heart disease and stroke were the top-ranked causes of DALYs in both the 50–74-year and 75-years-and-older age groups. Since 1990, there has been a marked shift towards a greater proportion of burden due to YLDs from non-communicable diseases and injuries. In 2019, there were 11 countries where non-communicable disease and injury YLDs constituted more than half of all disease burden. Decreases in age-standardised DALY rates have accelerated over the past decade in countries at the lower end of the SDI range, while improvements have started to stagnate or even reverse in countries with higher SDI. Interpretation: As disability becomes an increasingly large component of disease burden and a larger component of health expenditure, greater research and development investment is needed to identify new, more effective intervention strategies. With a rapidly ageing global population, the demands on health services to deal with disabling outcomes, which increase with age, will require policy makers to anticipate these changes. The mix of universal and more geographically specific influences on health reinforces the need for regular reporting on population health in detail and by underlying cause to help decision makers to identify success stories of disease control to emulate, as well as opportunities to improve. Funding: Bill & Melinda Gates Foundation. © 2020 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
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    Publication
    Global burden of 87 risk factors in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019
    (2020)
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    Zhao, Jeff T. (57221069965)
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    Zhao, Xiu-Ju George (8360350900)
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    Zhao, Yingxi (57194059646)
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    Lim, Stephen S. (57201800433)
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    Murray, Christopher J.L. (57224556036)
    Background: Rigorous analysis of levels and trends in exposure to leading risk factors and quantification of their effect on human health are important to identify where public health is making progress and in which cases current efforts are inadequate. The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2019 provides a standardised and comprehensive assessment of the magnitude of risk factor exposure, relative risk, and attributable burden of disease. Methods: GBD 2019 estimated attributable mortality, years of life lost (YLLs), years of life lived with disability (YLDs), and disability-adjusted life-years (DALYs) for 87 risk factors and combinations of risk factors, at the global level, regionally, and for 204 countries and territories. GBD uses a hierarchical list of risk factors so that specific risk factors (eg, sodium intake), and related aggregates (eg, diet quality), are both evaluated. This method has six analytical steps. (1) We included 560 risk–outcome pairs that met criteria for convincing or probable evidence on the basis of research studies. 12 risk–outcome pairs included in GBD 2017 no longer met inclusion criteria and 47 risk–outcome pairs for risks already included in GBD 2017 were added based on new evidence. (2) Relative risks were estimated as a function of exposure based on published systematic reviews, 81 systematic reviews done for GBD 2019, and meta-regression. (3) Levels of exposure in each age-sex-location-year included in the study were estimated based on all available data sources using spatiotemporal Gaussian process regression, DisMod-MR 2.1, a Bayesian meta-regression method, or alternative methods. (4) We determined, from published trials or cohort studies, the level of exposure associated with minimum risk, called the theoretical minimum risk exposure level. (5) Attributable deaths, YLLs, YLDs, and DALYs were computed by multiplying population attributable fractions (PAFs) by the relevant outcome quantity for each age-sex-location-year. (6) PAFs and attributable burden for combinations of risk factors were estimated taking into account mediation of different risk factors through other risk factors. Across all six analytical steps, 30 652 distinct data sources were used in the analysis. Uncertainty in each step of the analysis was propagated into the final estimates of attributable burden. Exposure levels for dichotomous, polytomous, and continuous risk factors were summarised with use of the summary exposure value to facilitate comparisons over time, across location, and across risks. Because the entire time series from 1990 to 2019 has been re-estimated with use of consistent data and methods, these results supersede previously published GBD estimates of attributable burden. Findings: The largest declines in risk exposure from 2010 to 2019 were among a set of risks that are strongly linked to social and economic development, including household air pollution; unsafe water, sanitation, and handwashing; and child growth failure. Global declines also occurred for tobacco smoking and lead exposure. The largest increases in risk exposure were for ambient particulate matter pollution, drug use, high fasting plasma glucose, and high body-mass index. In 2019, the leading Level 2 risk factor globally for attributable deaths was high systolic blood pressure, which accounted for 10·8 million (95% uncertainty interval [UI] 9·51–12·1) deaths (19·2% [16·9–21·3] of all deaths in 2019), followed by tobacco (smoked, second-hand, and chewing), which accounted for 8·71 million (8·12–9·31) deaths (15·4% [14·6–16·2] of all deaths in 2019). The leading Level 2 risk factor for attributable DALYs globally in 2019 was child and maternal malnutrition, which largely affects health in the youngest age groups and accounted for 295 million (253–350) DALYs (11·6% [10·3–13·1] of all global DALYs that year). The risk factor burden varied considerably in 2019 between age groups and locations. Among children aged 0–9 years, the three leading detailed risk factors for attributable DALYs were all related to malnutrition. Iron deficiency was the leading risk factor for those aged 10–24 years, alcohol use for those aged 25–49 years, and high systolic blood pressure for those aged 50–74 years and 75 years and older. Interpretation: Overall, the record for reducing exposure to harmful risks over the past three decades is poor. Success with reducing smoking and lead exposure through regulatory policy might point the way for a stronger role for public policy on other risks in addition to continued efforts to provide information on risk factor harm to the general public. Funding: Bill & Melinda Gates Foundation. © 2020 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
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    Publication
    Global Burden of Cardiovascular Diseases and Risk Factors, 1990-2019: Update From the GBD 2019 Study
    (2020)
    Roth, Gregory A. (55074747400)
    ;
    Mensah, George A. (57196028147)
    ;
    Johnson, Catherine O. (57212301236)
    ;
    Addolorato, Giovanni (7006562766)
    ;
    Ammirati, Enrico (25923325700)
    ;
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    Fuster, Valentin (7202675508)
    Cardiovascular diseases (CVDs), principally ischemic heart disease (IHD) and stroke, are the leading cause of global mortality and a major contributor to disability. This paper reviews the magnitude of total CVD burden, including 13 underlying causes of cardiovascular death and 9 related risk factors, using estimates from the Global Burden of Disease (GBD) Study 2019. GBD, an ongoing multinational collaboration to provide comparable and consistent estimates of population health over time, used all available population-level data sources on incidence, prevalence, case fatality, mortality, and health risks to produce estimates for 204 countries and territories from 1990 to 2019. Prevalent cases of total CVD nearly doubled from 271 million (95% uncertainty interval [UI]: 257 to 285 million) in 1990 to 523 million (95% UI: 497 to 550 million) in 2019, and the number of CVD deaths steadily increased from 12.1 million (95% UI:11.4 to 12.6 million) in 1990, reaching 18.6 million (95% UI: 17.1 to 19.7 million) in 2019. The global trends for disability-adjusted life years (DALYs) and years of life lost also increased significantly, and years lived with disability doubled from 17.7 million (95% UI: 12.9 to 22.5 million) to 34.4 million (95% UI:24.9 to 43.6 million) over that period. The total number of DALYs due to IHD has risen steadily since 1990, reaching 182 million (95% UI: 170 to 194 million) DALYs, 9.14 million (95% UI: 8.40 to 9.74 million) deaths in the year 2019, and 197 million (95% UI: 178 to 220 million) prevalent cases of IHD in 2019. The total number of DALYs due to stroke has risen steadily since 1990, reaching 143 million (95% UI: 133 to 153 million) DALYs, 6.55 million (95% UI: 6.00 to 7.02 million) deaths in the year 2019, and 101 million (95% UI: 93.2 to 111 million) prevalent cases of stroke in 2019. Cardiovascular diseases remain the leading cause of disease burden in the world. CVD burden continues its decades-long rise for almost all countries outside high-income countries, and alarmingly, the age-standardized rate of CVD has begun to rise in some locations where it was previously declining in high-income countries. There is an urgent need to focus on implementing existing cost-effective policies and interventions if the world is to meet the targets for Sustainable Development Goal 3 and achieve a 30% reduction in premature mortality due to noncommunicable diseases. © 2020 The Authors
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    Global, regional, and national age-sex specific mortality for 264 causes of death, 1980–2016: a systematic analysis for the Global Burden of Disease Study 2016
    (2017)
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    Vasankari, Tommi (57200592416)
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    Violante, Francesco S. (7003555890)
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    Vlassov, Vasiliy Victorovich (57211633239)
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    Vollset, Stein Emil (57196315778)
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    Vos, Theo (57223885848)
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    Wakayo, Tolassa (57205609717)
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    Wallin, Mitchell T. (57201573668)
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    Wang, Yuan-Pang (8576812100)
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    Weintraub, Robert G. (7006079405)
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    Weiss, Daniel J. (8609275600)
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    Xu, Gelin (57203583113)
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    Yaghoubi, Mohsen (57212400558)
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    Yano, Yuichiro (57196965200)
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    Yotebieng, Marcel (26325950800)
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    Zaidi, Zoubida (57197376721)
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    El Sayed Zaki, Maysaa (57203666922)
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    Zegeye, Elias Asfaw (57209171278)
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    Zenebe, Zerihun Menlkalew (57200737185)
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    Zerfu, Taddese Alemu (55358278900)
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    Zhang, Anthony Lin (56391112900)
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    Zhang, Xueying (56283378700)
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    Zodpey, Sanjay (7003415080)
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    Lopez, Alan D. (7401455668)
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    Murray, Christopher J.L. (55481130700)
    Background: Monitoring levels and trends in premature mortality is crucial to understanding how societies can address prominent sources of early death. The Global Burden of Disease 2016 Study (GBD 2016) provides a comprehensive assessment of cause-specifc mortality for 264 causes in 195 locations from 1980 to 2016. This assessment includes evaluation of the expected epidemiological transition with changes in development and where local patterns deviate from these trends. Methods: We estimated cause-specifc deaths and years of life lost (YLLs) by age, sex, geography, and year. YLLs were calculated from the sum of each death multiplied by the standard life expectancy at each age. We used the GBD cause of death database composed of: vital registration (VR) data corrected for under-registration and garbage coding; national and subnational verbal autopsy (VA) studies corrected for garbage coding; and other sources including surveys and surveillance systems for specifc causes such as maternal mortality. To facilitate assessment of quality, we reported on the fraction of deaths assigned to GBD Level 1 or Level 2 causes that cannot be underlying causes of death (major garbage codes) by location and year. Based on completeness, garbage coding, cause list detail, and time periods covered, we provided an overall data quality rating for each location with scores ranging from 0 stars (worst) to 5 stars (best). We used robust statistical methods including the Cause of Death Ensemble model (CODEm) to generate estimates for each location, year, age, and sex. We assessed observed and expected levels and trends of cause-specifc deaths in relation to the Socio-demographic Index (SDI), a summary indicator derived from measures of average income per capita, educational attainment, and total fertility, with locations grouped into quintiles by SDI. Relative to GBD 2015, we expanded the GBD cause hierarchy by 18 causes of death for GBD 2016. Findings: The quality of available data varied by location. Data quality in 25 countries rated in the highest category (5 stars), while 48, 30, 21, and 44 countries were rated at each of the succeeding data quality levels. Vital registration or verbal autopsy data were not available in 27 countries, resulting in the assignment of a zero value for data quality. Deaths from non-communicable diseases (NCDs) represented 72·3% (95% uncertainty interval [UI] 71·2-73·2) of deaths in 2016 with 19·3% (18·5-20·4) of deaths in that year occurring from communicable, maternal, neonatal, and nutritional (CMNN) diseases and a further 8·43% (8·00-8·67) from injuries. Although age-standardised rates of death from NCDs decreased globally between 2006 and 2016, total numbers of these deaths increased; both numbers and age-standardised rates of death from CMNN causes decreased in the decade 2006-16 - age-standardised rates of deaths from injuries decreased but total numbers varied little. In 2016, the three leading global causes of death in children under-5 were lower respiratory infections, neonatal preterm birth complications, and neonatal encephalopathy due to birth asphyxia and trauma, combined resulting in 1·80 million deaths (95% UI 1·59 million to 1·89 million). Between 1990 and 2016, a profound shift toward deaths at older ages occurred with a 178% (95% UI 176-181) increase in deaths in ages 90-94 years and a 210% (208-212) increase in deaths older than age 95 years. The ten leading causes by rates of age-standardised YLL signifcantly decreased from 2006 to 2016 (median annualised rate of change was a decrease of 2·89%); the median annualised rate of change for all other causes was lower (a decrease of 1·59%) during the same interval. Globally, the fve leading causes of total YLLs in 2016 were cardiovascular diseases; diarrhoea, lower respiratory infections, and other common infectious diseases; neoplasms; neonatal disorders; and HIV/AIDS and tuberculosis. At a fner level of disaggregation within cause groupings, the ten leading causes of total YLLs in 2016 were ischaemic heart disease, cerebrovascular disease, lower respiratory infections, diarrhoeal diseases, road injuries, malaria, neonatal preterm birth complications, HIV/AIDS, chronic obstructive pulmonary disease, and neonatal encephalopathy due to birth asphyxia and trauma. Ischaemic heart disease was the leading cause of total YLLs in 113 countries for men and 97 countries for women. Comparisons of observed levels of YLLs by countries, relative to the level of YLLs expected on the basis of SDI alone, highlighted distinct regional patterns including the greater than expected level of YLLs from malaria and from HIV/AIDS across sub-Saharan Africa; diabetes mellitus, especially in Oceania; interpersonal violence, notably within Latin America and the Caribbean; and cardiomyopathy and myocarditis, particularly in eastern and central Europe. The level of YLLs from ischaemic heart disease was less than expected in 117 of 195 locations. Other leading causes of YLLs for which YLLs were notably lower than expected included neonatal preterm birth complications in many locations in both south Asia and southeast Asia, and cerebrovascular disease in western Europe. Interpretation: The past 37 years have featured declining rates of communicable, maternal, neonatal, and nutritional diseases across all quintiles of SDI, with faster than expected gains for many locations relative to their SDI. A global shift towards deaths at older ages suggests success in reducing many causes of early death. YLLs have increased globally for causes such as diabetes mellitus or some neoplasms, and in some locations for causes such as drug use disorders, and confict and terrorism. Increasing levels of YLLs might refect outcomes from conditions that required high levels of care but for which efective treatments remain elusive, potentially increasing costs to health systems. Copyright © 2017 The Author(s). Published by Elsevier Ltd.
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    Global, regional, and national age-sex-specific mortality and life expectancy, 1950-2017: A systematic analysis for the Global Burden of Disease Study 2017
    (2018)
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    Shams-Beyranvand, Mehran (57193608415)
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    Shamsizadeh, Morteza (57195940127)
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    Sharafi, Kiomars (57194516056)
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    Sharif, Mehdi (16022734200)
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    Sharif-Alhoseini, Mahdi (35108018000)
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    Sharma, Meenakshi (58730797800)
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    Sharma, Jayendra (57195329457)
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    Sharma, Rajesh (58228412600)
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    She, Jun (57209122131)
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    Sheikh, Aziz (7202522962)
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    Sheth, Kevin N. (57212863894)
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    Shi, Peilin (57203064901)
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    Shibuya, Kenji (8948057900)
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    Shifa, Girma Temam (57211793093)
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    Shiferaw, Mekonnen Sisay (57205232012)
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    Shigematsu, Mika (23968093000)
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    Shiri, Rahman (57200737050)
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    Shirkoohi, Reza (12776374400)
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    Shiue, Ivy (35811219800)
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    Shokraneh, Farhad (36146063000)
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    Shrime, Mark G. (57204703404)
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    Shukla, Sharvari Rahul (55760856000)
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    Si, Si (56706979500)
    Background: Assessments of age-specifc mortality and life expectancy have been done by the UN Population Division, Department of Economics and Social Afairs (UNPOP), the United States Census Bureau, WHO, and as part of previous iterations of the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD). Previous iterations of the GBD used population estimates from UNPOP, which were not derived in a way that was internally consistent with the estimates of the numbers of deaths in the GBD. The present iteration of the GBD, GBD 2017, improves on previous assessments and provides timely estimates of the mortality experience of populations globally. Methods: The GBD uses all available data to produce estimates of mortality rates between 1950 and 2017 for 23 age groups, both sexes, and 918 locations, including 195 countries and territories and subnational locations for 16 countries. Data used include vital registration systems, sample registration systems, household surveys (complete birth histories, summary birth histories, sibling histories), censuses (summary birth histories, household deaths), and Demographic Surveillance Sites. In total, this analysis used 8259 data sources. Estimates of the probability of death between birth and the age of 5 years and between ages 15 and 60 years are generated and then input into a model life table system to produce complete life tables for all locations and years. Fatal discontinuities and mortality due to HIV/AIDS are analysed separately and then incorporated into the estimation. We analyse the relationship between age-specifc mortality and development status using the Socio-demographic Index, a composite measure based on fertility under the age of 25 years, education, and income. There are four main methodological improvements in GBD 2017 compared with GBD 2016: 622 additional data sources have been incorporated; new estimates of population, generated by the GBD study, are used; statistical methods used in diferent components of the analysis have been further standardised and improved; and the analysis has been extended backwards in time by two decades to start in 1950. Findings: Globally, 18·7% (95% uncertainty interval 18·4-19·0) of deaths were registered in 1950 and that proportion has been steadily increasing since, with 58·8% (58·2-59·3) of all deaths being registered in 2015. At the global level, between 1950 and 2017, life expectancy increased from 48·1 years (46·5-49·6) to 70·5 years (70·1-70·8) for men and from 52·9 years (51·7-54·0) to 75·6 years (75·3-75·9) for women. Despite this overall progress, there remains substantial variation in life expectancy at birth in 2017, which ranges from 49·1 years (46·5-51·7) for men in the Central African Republic to 87·6 years (86·9-88·1) among women in Singapore. The greatest progress across age groups was for children younger than 5 years; under-5 mortality dropped from 216·0 deaths (196·3-238·1) per 1000 livebirths in 1950 to 38·9 deaths (35·6-42·83) per 1000 livebirths in 2017, with huge reductions across countries. Nevertheless, there were still 5·4 million (5·2-5·6) deaths among children younger than 5 years in the world in 2017. Progress has been less pronounced and more variable for adults, especially for adult males, who had stagnant or increasing mortality rates in several countries. The gap between male and female life expectancy between 1950 and 2017, while relatively stable at the global level, shows distinctive patterns across super-regions and has consistently been the largest in central Europe, eastern Europe, and central Asia, and smallest in south Asia. Performance was also variable across countries and time in observed mortality rates compared with those expected on the basis of development. Interpretation: This analysis of age-sex-specifc mortality shows that there are remarkably complex patterns in population mortality across countries. The fndings of this study highlight global successes, such as the large decline in under-5 mortality, which refects signifcant local, national, and global commitment and investment over several decades. However, they also bring attention to mortality patterns that are a cause for concern, particularly among adult men and, to a lesser extent, women, whose mortality rates have stagnated in many countries over the time period of this study, and in some cases are increasing. © 2018 The Author(s).
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    Publication
    Global, regional, and national age-sex-specific mortality for 282 causes of death in 195 countries and territories, 1980–2017: a systematic analysis for the Global Burden of Disease Study 2017
    (2018)
    Roth, Gregory A. (55074747400)
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    Abate, Degu (57204237665)
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    Abate, Kalkidan Hassen (57207943858)
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    Abay, Solomon M. (35306466900)
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    Abbafati, Cristiana (54917122400)
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    Abbasi, Nooshin (57212442022)
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    Abbastabar, Hedayat (57212441848)
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    Abd-Allah, Foad (36503428900)
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    Abdela, Jemal (57200613000)
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    Abdelalim, Ahmed (7801307783)
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    Abdollahpour, Ibrahim (36997151900)
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    Abdulkader, Rizwan Suliankatchi (57195295816)
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    Abebe, Haftom Temesgen (55950002100)
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    Abebe, Molla (57211131124)
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    Abebe, Zegeye (57193002719)
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    Abejie, Ayenew Negesse (57203015573)
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    Abera, Semaw F. (57205180598)
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    Abil, Olifan Zewdie (57204558002)
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    Abraha, Haftom Niguse (57195289877)
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    Abrham, Aklilu Roba (57202704637)
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    Abu-Raddad, Laith Jamal (14032724700)
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    Accrombessi, Manfred Mario Kokou (55353650500)
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    Acharya, Dilaram (56770895600)
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    Adamu, Abdu A. (57202024381)
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    Whiteford, Harvey A. (55906494000)
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    Widecka, Justyna (15047205800)
    Background: Global development goals increasingly rely on country-specific estimates for benchmarking a nation's progress. To meet this need, the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2016 estimated global, regional, national, and, for selected locations, subnational cause-specific mortality beginning in the year 1980. Here we report an update to that study, making use of newly available data and improved methods. GBD 2017 provides a comprehensive assessment of cause-specific mortality for 282 causes in 195 countries and territories from 1980 to 2017. Methods: The causes of death database is composed of vital registration (VR), verbal autopsy (VA), registry, survey, police, and surveillance data. GBD 2017 added ten VA studies, 127 country-years of VR data, 502 cancer-registry country-years, and an additional surveillance country-year. Expansions of the GBD cause of death hierarchy resulted in 18 additional causes estimated for GBD 2017. Newly available data led to subnational estimates for five additional countries—Ethiopia, Iran, New Zealand, Norway, and Russia. Deaths assigned International Classification of Diseases (ICD) codes for non-specific, implausible, or intermediate causes of death were reassigned to underlying causes by redistribution algorithms that were incorporated into uncertainty estimation. We used statistical modelling tools developed for GBD, including the Cause of Death Ensemble model (CODEm), to generate cause fractions and cause-specific death rates for each location, year, age, and sex. Instead of using UN estimates as in previous versions, GBD 2017 independently estimated population size and fertility rate for all locations. Years of life lost (YLLs) were then calculated as the sum of each death multiplied by the standard life expectancy at each age. All rates reported here are age-standardised. Findings: At the broadest grouping of causes of death (Level 1), non-communicable diseases (NCDs) comprised the greatest fraction of deaths, contributing to 73·4% (95% uncertainty interval [UI] 72·5–74·1) of total deaths in 2017, while communicable, maternal, neonatal, and nutritional (CMNN) causes accounted for 18·6% (17·9–19·6), and injuries 8·0% (7·7–8·2). Total numbers of deaths from NCD causes increased from 2007 to 2017 by 22·7% (21·5–23·9), representing an additional 7·61 million (7·20–8·01) deaths estimated in 2017 versus 2007. The death rate from NCDs decreased globally by 7·9% (7·0–8·8). The number of deaths for CMNN causes decreased by 22·2% (20·0–24·0) and the death rate by 31·8% (30·1–33·3). Total deaths from injuries increased by 2·3% (0·5–4·0) between 2007 and 2017, and the death rate from injuries decreased by 13·7% (12·2–15·1) to 57·9 deaths (55·9–59·2) per 100 000 in 2017. Deaths from substance use disorders also increased, rising from 284 000 deaths (268 000–289 000) globally in 2007 to 352 000 (334 000–363 000) in 2017. Between 2007 and 2017, total deaths from conflict and terrorism increased by 118·0% (88·8–148·6). A greater reduction in total deaths and death rates was observed for some CMNN causes among children younger than 5 years than for older adults, such as a 36·4% (32·2–40·6) reduction in deaths from lower respiratory infections for children younger than 5 years compared with a 33·6% (31·2–36·1) increase in adults older than 70 years. Globally, the number of deaths was greater for men than for women at most ages in 2017, except at ages older than 85 years. Trends in global YLLs reflect an epidemiological transition, with decreases in total YLLs from enteric infections, respiratory infections and tuberculosis, and maternal and neonatal disorders between 1990 and 2017; these were generally greater in magnitude at the lowest levels of the Socio-demographic Index (SDI). At the same time, there were large increases in YLLs from neoplasms and cardiovascular diseases. YLL rates decreased across the five leading Level 2 causes in all SDI quintiles. The leading causes of YLLs in 1990—neonatal disorders, lower respiratory infections, and diarrhoeal diseases—were ranked second, fourth, and fifth, in 2017. Meanwhile, estimated YLLs increased for ischaemic heart disease (ranked first in 2017) and stroke (ranked third), even though YLL rates decreased. Population growth contributed to increased total deaths across the 20 leading Level 2 causes of mortality between 2007 and 2017. Decreases in the cause-specific mortality rate reduced the effect of population growth for all but three causes: substance use disorders, neurological disorders, and skin and subcutaneous diseases. Interpretation: Improvements in global health have been unevenly distributed among populations. Deaths due to injuries, substance use disorders, armed conflict and terrorism, neoplasms, and cardiovascular disease are expanding threats to global health. For causes of death such as lower respiratory and enteric infections, more rapid progress occurred for children than for the oldest adults, and there is continuing disparity in mortality rates by sex across age groups. Reductions in the death rate of some common diseases are themselves slowing or have ceased, primarily for NCDs, and the death rate for selected causes has increased in the past decade. Funding: Bill & Melinda Gates Foundation. © 2018 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
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    Global, regional, and national comparative risk assessment of 84 behavioural, environmental and occupational, and metabolic risks or clusters of risks, 1990-2016: A systematic analysis for the Global Burden of Disease Study 2016
    (2017)
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    Bhutta, Zulfqar A. (24342648300)
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    Carrero, Juan Jesus (16834646800)
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    Chisumpa, Vesper Hichilombwe (56761895800)
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    Duncan, Bruce Bartholow (35476478500)
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    Tabarés-Seisdedos, Rafael (6602981102)
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    Tadakamadla, Santosh Kumar (57207799926)
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    Takahashi, Ken (55741242600)
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    Takala, Jukka S. (35425471300)
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    Tandon, Nikhil (7101833756)
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    Tanner, Marcel (7202127772)
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    Tarekegn, Yihunie L. (57202809688)
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    Tavakkoli, Mohammad (57202524239)
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    Tegegne, Teketo Kassaw (57216998561)
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    Tehrani-Banihashemi, Arash (57204006020)
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    Terkawi, Abdullah Sulieman (57211144258)
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    Tesssema, Belay (57195294962)
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    Thakur, J.S. (57204002123)
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    Thamsuwan, Ornwipa (55484605700)
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    Thankappan, Kavumpurathu Raman (57202955435)
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    Theis, Andrew M. (57196076787)
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    Thomas, Matthew Lloyd (57191835351)
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    Thomson, Alan J. (57969994200)
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    Thrift, Amanda G. (7004824524)
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    Tillmann, Taavi (57190211142)
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    Tobollik, Myriam (56549045300)
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    Tollanes, Mette C. (16833860000)
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    Tonelli, Marcello (7103102534)
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    Topor-Madry, Roman (57211182892)
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    Torre, Anna (57196074351)
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    Tortajada, Miguel (16242320900)
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    Touvier, Mathilde (8877033300)
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    Tran, Bach Xuan (57209107515)
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    Truelsen, Thomas (57202824565)
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    Tuem, Kald Beshir (57216106503)
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    Tuzcu, Emin Murat (7005951350)
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    Tyrovolas, Stefanos (57207793475)
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    Ukwaja, Kingsley Nnanna (57202824584)
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    Uneke, Chigozie Jesse (57202824589)
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    Updike, Rachel (57204698680)
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    Uthman, Olalekan A. (23026328100)
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    Van Boven, Job F.M. (53464198500)
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    Van Donkelaar, Aaron (15926418500)
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    Varughese, Santosh (22942817500)
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    Vasankari, Tommi (57200592416)
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    Veerman, Lennert J. (8222114200)
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    Venkateswaran, Vidhya (59829999400)
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    Venketasubramanian, Narayanaswamy (56804702100)
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    Violante, Francesco S. (7003555890)
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    Vladimirov, Sergey K. (57195959162)
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    Vlassov, Vasiliy Victorovich (57211633239)
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    Vollset, Stein Emil (57196315778)
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    Vos, Theo (57223885848)
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    Wadilo, Fiseha (57194049305)
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    Wakayo, Tolassa (57205609717)
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    Wallin, Mitchell T. (57201573668)
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    Wang, Yuan-Pang (8576812100)
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    Weichenthal, Scott (57202555239)
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    Weiderpass, Elisabete (57205018947)
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    Weintraub, Robert G. (7006079405)
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    Weiss, Daniel J. (8609275600)
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    Werdecker, Andrea (57208964895)
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    Westerman, Ronny (57218361023)
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    Whiteford, Harvey A. (55906494000)
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    Wiysonge, Charles Shey (6507441509)
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    Woldeyes, Belete Getahun (57195329524)
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    Wolfe, Charles D.A. (57202754705)
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    Woodbrook, Rachel (57200298006)
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    Workicho, Abdulhalik (56720337100)
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    Wulf Hanson, Sarah (57212263269)
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    Xavier, Denis (55403963100)
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    Xu, Gelin (57203583113)
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    Yadgir, Simon (57192837280)
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    Yakob, Bereket (57203811497)
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    Yan, Lijing L. (57198311895)
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    Yaseri, Mehdi (23029507000)
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    Yimam, Hassen Hamid (57196325590)
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    Yip, Paul (7102503720)
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    Yonemoto, Naohiro (57204947657)
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    Yoon, Seok-Jun (24823148900)
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    Yotebieng, Marcel (26325950800)
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    Younis, Mustafa Z. (8549393000)
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    Zaidi, Zoubida (57197376721)
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    El Sayed Zaki, Maysaa (57203666922)
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    Zavala-Arciniega, Luis (57196083471)
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    Zhang, Xueying (56283378700)
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    Zimsen, Stephanie Raman M. (57196078433)
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    Zipkin, Ben (57200737130)
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    Zodpey, Sanjay (7003415080)
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    Lim, Stephen S. (57201800433)
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    Murray, Christopher J.L. (55481130700)
    Background: The Global Burden of Diseases, Injuries, and Risk Factors Study 2016 (GBD 2016) provides a comprehensive assessment of risk factor exposure and attributable burden of disease. By providing estimates over a long time series, this study can monitor risk exposure trends critical to health surveillance and inform policy debates on the importance of addressing risks in context. Methods: We used the comparative risk assessment framework developed for previous iterations of GBD to estimate levels and trends in exposure, attributable deaths, and attributable disability-adjusted life-years (DALYs), by age group, sex, year, and location for 84 behavioural, environmental and occupational, and metabolic risks or clusters of risks from 1990 to 2016. This study included 481 risk-outcome pairs that met the GBD study criteria for convincing or probable evidence of causation. We extracted relative risk (RR) and exposure estimates from 22 717 randomised controlled trials, cohorts, pooled cohorts, household surveys, census data, satellite data, and other sources, according to the GBD 2016 source counting methods. Using the counterfactual scenario of theoretical minimum risk exposure level (TMREL), we estimated the portion of deaths and DALYs that could be attributed to a given risk. Finally, we explored four drivers of trends in attributable burden: population growth, population ageing, trends in risk exposure, and all other factors combined. Findings: Since 1990, exposure increased significantly for 30 risks, did not change significantly for four risks, and decreased significantly for 31 risks. Among risks that are leading causes of burden of disease, child growth failure and household air pollution showed the most significant declines, while metabolic risks, such as body-mass index and high fasting plasma glucose, showed significant increases. In 2016, at Level 3 of the hierarchy, the three leading risk factors in terms of attributable DALYs at the global level for men were smoking (124.1 million DALYs [95% UI 111.2 million to 137.0 million]), high systolic blood pressure (122.2 million DALYs [110.3 million to 133.3 million], and low birthweight and short gestation (83.0 million DALYs [78.3 million to 87.7 million]), and for women, were high systolic blood pressure (89.9 million DALYs [80.9 million to 98.2 million]), high body-mass index (64.8 million DALYs [44.4 million to 87.6 million]), and high fasting plasma glucose (63.8 million DALYs [53.2 million to 76.3 million]). In 2016 in 113 countries, the leading risk factor in terms of attributable DALYs was a metabolic risk factor. Smoking remained among the leading five risk factors for DALYs for 109 countries, while low birthweight and short gestation was the leading risk factor for DALYs in 38 countries, particularly in sub-Saharan Africa and South Asia. In terms of important drivers of change in trends of burden attributable to risk factors, between 2006 and 2016 exposure to risks explains an 9.3% (6.9-11.6) decline in deaths and a 10.8% (8.3-13.1) decrease in DALYs at the global level, while population ageing accounts for 14.9% (12.7-17.5) of deaths and 6.2% (3.9-8.7) of DALYs, and population growth for 12.4% (10.1-14.9) of deaths and 12.4% (10.1-14.9) of DALYs. The largest contribution of trends in risk exposure to disease burden is seen between ages 1 year and 4 years, where a decline of 27.3% (24.9-29.7) of the change in DALYs between 2006 and 2016 can be attributed to declines in exposure to risks. Interpretation: Increasingly detailed understanding of the trends in risk exposure and the RRs for each risk-outcome pair provide insights into both the magnitude of health loss attributable to risks and how modification of risk exposure has contributed to health trends. Metabolic risks warrant particular policy attention, due to their large contribution to global disease burden, increasing trends, and variable patterns across countries at the same level of development. GBD 2016 findings show that, while it has huge potential to improve health, risk modification has played a relatively small part in the past decade. © The Author(s). Published by Elsevier Ltd.
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    Global, regional, and national disability-adjusted life years (DALYs) for 306 diseases and injuries and healthy life expectancy (HALE) for 188 countries, 1990-2013: Quantifying the epidemiological transition
    (2015)
    Murray, Christopher J. L. (57224556036)
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    Barber, Ryan M. (57202560423)
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    Foreman, Kyle J. (57209064414)
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    Abera, Semaw F. (57205180598)
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    Aboyans, Victor (56214736500)
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    Abubakar, Ibrahim (57220174401)
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    Wang, Haidong (16507828100)
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    Wang, Jianli (9250575900)
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    Xu, Gelin (57203583113)
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    Yan, Lijing L. (57198311895)
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    Yano, Yuichiro (57196965200)
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    Ye, Pengpeng (57202839295)
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    Younis, Mustafa Z. (8549393000)
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    Yu, Chuanhua (57201889726)
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    Zaki, Maysaa E. (57203666922)
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    Zhao, Yong (59798995400)
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    Zheng, Yingfeng (58918045300)
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    Zonies, David (6507066392)
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    Zou, Xiaonong (57216284159)
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    Salomon, Joshua A. (56745638600)
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    Lopez, Alan D. (7401455668)
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    Vos, Theo (57223885848)
    Background The Global Burden of Disease Study 2013 (GBD 2013) aims to bring together all available epidemiological data using a coherent measurement framework, standardised estimation methods, and transparent data sources to enable comparisons of health loss over time and across causes, age-sex groups, and countries. The GBD can be used to generate summary measures such as disability-adjusted life-years (DALYs) and healthy life expectancy (HALE) that make possible comparative assessments of broad epidemiological patterns across countries and time. These summary measures can also be used to quantify the component of variation in epidemiology that is related to sociodemographic development. Methods We used the published GBD 2013 data for age-specific mortality, years of life lost due to premature mortality (YLLs), and years lived with disability (YLDs) to calculate DALYs and HALE for 1990, 1995, 2000, 2005, 2010, and 2013 for 188 countries. We calculated HALE using the Sullivan method; 95% uncertainty intervals (UIs) represent uncertainty in age-specific death rates and YLDs per person for each country, age, sex, and year. We estimated DALYs for 306 causes for each country as the sum of YLLs and YLDs; 95% UIs represent uncertainty in YLL and YLD rates. We quantified patterns of the epidemiological transition with a composite indicator of sociodemographic status, which we constructed from income per person, average years of schooling after age 15 years, and the total fertility rate and mean age of the population. We applied hierarchical regression to DALY rates by cause across countries to decompose variance related to the sociodemographic status variable, country, and time. Findings Worldwide, from 1990 to 2013, life expectancy at birth rose by 6·2 years (95% UI 5·6-6·6), from 65·3 years (65·0-65·6) in 1990 to 71·5 years (71·0-71·9) in 2013, HALE at birth rose by 5·4 years (4·9-5·8), from 56·9 years (54·5-59·1) to 62·3 years (59·7-64·8), total DALYs fell by 3·6% (0·3-7·4), and age-standardised DALY rates per 100 000 people fell by 26·7% (24·6-29·1). For communicable, maternal, neonatal, and nutritional disorders, global DALY numbers, crude rates, and age-standardised rates have all declined between 1990 and 2013, whereas for non-communicable diseases, global DALYs have been increasing, DALY rates have remained nearly constant, and age-standardised DALY rates declined during the same period. From 2005 to 2013, the number of DALYs increased for most specific non-communicable diseases, including cardiovascular diseases and neoplasms, in addition to dengue, food-borne trematodes, and leishmaniasis; DALYs decreased for nearly all other causes. By 2013, the five leading causes of DALYs were ischaemic heart disease, lower respiratory infections, cerebrovascular disease, low back and neck pain, and road injuries. Sociodemographic status explained more than 50% of the variance between countries and over time for diarrhoea, lower respiratory infections, and other common infectious diseases; maternal disorders; neonatal disorders; nutritional deficiencies; other communicable, maternal, neonatal, and nutritional diseases; musculoskeletal disorders; and other non-communicable diseases. However, sociodemographic status explained less than 10% of the variance in DALY rates for cardiovascular diseases; chronic respiratory diseases; cirrhosis; diabetes, urogenital, blood, and endocrine diseases; unintentional injuries; and self-harm and interpersonal violence. Predictably, increased sociodemographic status was associated with a shift in burden from YLLs to YLDs, driven by declines in YLLs and increases in YLDs from musculoskeletal disorders, neurological disorders, and mental and substance use disorders. In most country-specific estimates, the increase in life expectancy was greater than that in HALE. Leading causes of DALYs are highly variable across countries. Interpretation Global health is improving. Population growth and ageing have driven up numbers of DALYs, but crude rates have remained relatively constant, showing that progress in health does not mean fewer demands on health systems. The notion of an epidemiological transition - in which increasing sociodemographic status brings structured change in disease burden - is useful, but there is tremendous variation in burden of disease that is not associated with sociodemographic status. This further underscores the need for country-specific assessments of DALYs and HALE to appropriately inform health policy decisions and attendant actions. © 2015 Elsevier Ltd.
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    Publication
    Global, regional, and national disability-adjusted life-years (DALYs) for 333 diseases and injuries and healthy life expectancy (HALE) for 195 countries and territories, 1990-2016: A systematic analysis for the Global Burden of Disease Study 2016
    (2017)
    Hay, Simon I. (7101875313)
    ;
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    Zaki, Maysaa El Sayed (57203666922)
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    Zegeye, Elias Asfaw (57209171278)
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    Zenebe, Zerihun Menlkalew (57200737185)
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    Zhang, Xueying (56283378700)
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    Zheng, Yingfeng (58918045300)
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    Zhou, Maigeng (57054557200)
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    Zipkin, Ben (57200737130)
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    Zodpey, Sanjay (7003415080)
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    Zoeckler, Leo (57203905510)
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    Zuhlke, Liesl Joanna (57209027746)
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    Murray, Christopher J. L. (55481130700)
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    Adedji, I.A. (57207919805)
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    Murdoch, M.E. (57202097865)
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    Bryane, C.E.G. (57207920084)
    Background: Measurement of changes in health across locations is useful to compare and contrast changing epidemiological patterns against health system performance and identify specific needs for resource allocation in research, policy development, and programme decision making. Using the Global Burden of Diseases, Injuries, and Risk Factors Study 2016, we drew from two widely used summary measures to monitor such changes in population health: disability-adjusted life-years (DALYs) and healthy life expectancy (HALE). We used these measures to track trends and benchmark progress compared with expected trends on the basis of the Socio-demographic Index (SDI). Methods: We used results from the Global Burden of Diseases, Injuries, and Risk Factors Study 2016 for all-cause mortality, cause-specific mortality, and non-fatal disease burden to derive HALE and DALYs by sex for 195 countries and territories from 1990 to 2016. We calculated DALYs by summing years of life lost and years of life lived with disability for each location, age group, sex, and year. We estimated HALE using age-specific death rates and years of life lived with disability per capita. We explored how DALYs and HALE difered from expected trends when compared with the SDI: the geometric mean of income per person, educational attainment in the population older than age 15 years, and total fertility rate. Findings: The highest globally observed HALE at birth for both women and men was in Singapore, at 75·2 years (95% uncertainty interval 71·9-78·6) for females and 72·0 years (68·8-75·1) for males. The lowest for females was in the Central African Republic (45·6 years [42·0-49·5]) and for males was in Lesotho (41·5 years [39·0-44·0]). From 1990 to 2016, global HALE increased by an average of 6·24 years (5·97-6·48) for both sexes combined. Global HALE increased by 6·04 years (5·74-6·27) for males and 6·49 years (6·08-6·77) for females, whereas HALE at age 65 years increased by 1·78 years (1·61-1·93) for males and 1·96 years (1·69-2·13) for females. Total global DALYs remained largely unchanged from 1990 to 2016 (-2·3% [-5·9 to 0·9]), with decreases in communicable, maternal, neonatal, and nutritional (CMNN) disease DALYs ofset by increased DALYs due to non-communicable diseases (NCDs). The exemplars, calculated as the fve lowest ratios of observed to expected age-standardised DALY rates in 2016, were Nicaragua, Costa Rica, the Maldives, Peru, and Israel. The leading three causes of DALYs globally were ischaemic heart disease, cerebrovascular disease, and lower respiratory infections, comprising 16·1% of all DALYs. Total DALYs and age-standardised DALY rates due to most CMNN causes decreased from 1990 to 2016. Conversely, the total DALY burden rose for most NCDs; however, age-standardised DALY rates due to NCDs declined globally. Interpretation: At a global level, DALYs and HALE continue to show improvements. At the same time, we observe that many populations are facing growing functional health loss. Rising SDI was associated with increases in cumulative years of life lived with disability and decreases in CMNN DALYs ofset by increased NCD DALYs. Relative compression of morbidity highlights the importance of continued health interventions, which has changed in most locations in pace with the gross domestic product per person, education, and family planning. The analysis of DALYs and HALE and their relationship to SDI represents a robust framework with which to benchmark location-specific health performance. Country-specific drivers of disease burden, particularly for causes with higher-than-expected DALYs, should inform health policies, health system improvement initiatives, targeted prevention eforts, and development assistance for health, including fnancial and research investments for all countries, regardless of their level of sociodemographic development. The presence of countries that substantially outperform others suggests the need for increased scrutiny for proven examples of best practices, which can help to extend gains, whereas the presence of underperforming countries suggests the need for devotion of extra attention to health systems that need more robust support. © The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license.
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    Global, regional, and national disability-adjusted life-years (DALYs) for 359 diseases and injuries and healthy life expectancy (HALE) for 195 countries and territories, 1990-2017: A systematic analysis for the Global Burden of Disease Study 2017
    (2018)
    Kyu, Hmwe Hmwe (57217040073)
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    Abate, Degu (57204237665)
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    Abate, Kalkidan Hassen (57207943858)
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    Abay, Solomon M. (35306466900)
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    Abbafati, Cristiana (54917122400)
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    Abbasi, Nooshin (57212442022)
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    Abbastabar, Hedayat (57212441848)
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    Abd-Allah, Foad (36503428900)
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    Abdela, Jemal (57200613000)
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    Abdelalim, Ahmed (7801307783)
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    Abdollahpour, Ibrahim (36997151900)
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    Abdulkader, Rizwan Suliankatchi (57195295816)
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    Abebe, Molla (57211131124)
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    Abebe, Zegeye (57193002719)
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    Abil, Olifan Zewdie (57204558002)
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    Aboyans, Victor (56214736500)
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    Abu-Raddad, Laith Jamal (14032724700)
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    Abu-Rmeileh, Niveen M.E. (57216675148)
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    Murray, Christopher J.L. (55481130700)
    Background: How long one lives, how many years of life are spent in good and poor health, and how the population's state of health and leading causes of disability change over time all have implications for policy, planning, and provision of services. We comparatively assessed the patterns and trends of healthy life expectancy (HALE), which quantifies the number of years of life expected to be lived in good health, and the complementary measure of disability-adjusted lifeyears (DALYs), a composite measure of disease burden capturing both premature mortality and prevalence and severityof ill health, for 359 diseases and injuries for 195 countries and territories over the past 28 years. Methods We used data for age-speci?c mortality rates, years of life lost (YLLs) due to premature mortality, and years lived with disability (YLDs) from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2017 to calculate HALE and DALYs from 1990 to 2017. We calculated HALE using age-specific mortality rates and YLDs per capita for each location, age, sex, and year. We calculated DALYs for 359 causes as the sum of YLLs and YLDs. We assessed how observed HALE and DALYs differed by country and sex from expected trends based on Sociodemographic Index (SDI). We also analysed HALE by decomposing years of life gained into years spent in good health and in poor health, between 1990 and 2017, and extra years lived by females compared with males. Findings Globally, from 1990 to 2017, life expectancy at birth increased by 7·4 years (95% uncertainty interval 7·1-7·8), from 65·6 years (65·3-65·8) in 1990 to 73·0 years (72·7-73·3) in 2017. The increase in years of life varied from 5·1 years (5·0-5·3) in high SDI countries to 12·0 years (11·3-12·8) in low SDI countries. Of the additional years of life expected at birth, 26·3% (20·1-33·1) were expected to be spent in poor health in high SDI countries compared with 11·7% (8·8-15·1) in low-middle SDI countries. HALE at birth increased by 6·3 years (5·9-6·7), from 57·0 years (54·6-59·1) in 1990 to 63·3 years (60·5-65·7) in 2017. The increase varied from 3·8 years (3·4-4·1) in high SDI countries to 10·5 years (9·8-11·2) in low SDI countries. Even larger variations in HALE than these were observed between countries, ranging from 1·0 year (0·4-1·7) in Saint Vincent and the Grenadines (62·4 years [59·9-64·7] in 1990 to 63·5 years [60·9-65·8] in 2017) to 23·7 years (21·9-25·6) in Eritrea (30·7 years [28·9-32·2] in 1990 to 54·4 years [51·5-57·1] in 2017). In most countries, the increase in HALE was smaller than the increase in overall life expectancy, indicating more years lived in poor health. In 180 of 195 countries and territories, females were expected to live longer than males in 2017, with extra years lived varying from 1·4 years (0·6-2·3) in Algeria to 11·9 years (10·9-12·9) in Ukraine. Of the extra years gained, the proportion spent in poor health varied largely across countries, with less than 20% of additional years spent in poor health in Bosnia and Herzegovina, Burundi, and Slovakia, whereas in Bahrain all the extra years were spent in poor health. In 2017, the highest estimate of HALE at birth was in Singapore for both females (75·8 years [72·4-78·7]) and males (72·6 years [69·8-75·0]) and the lowest estimates were in Central African Republic (47·0 years [43·7-50·2] for females and 42·8 years [40·1-45·6] for males). Globally, in 2017, the ?ve leading causes of DALYs were neonatal disorders, ischaemic heart disease, stroke, lower respiratory infections, and chronic obstructive pulmonary disease. Between 1990 and 2017, age-standardised DALY rates decreased by 41·3% (38·8-43·5) for communicable diseases and by 49·8% (47·9-51·6) for neonatal disorders. For non-communicable diseases, global DALYs increased by 40·1% (36·8-43·0), although age-standardised DALY rates decreased by 18·1% (16·0-20·2). Interpretation With increasing life expectancy in most countries, the question of whether the additional years of life gained are spent in good health or poor health has been increasingly relevant because of the potential policy implications, such as health-care provisions and extending retirement ages. In some locations, a large proportion of those additional years are spent in poor health. Large inequalities in HALE and disease burden exist across countries in different SDI quintiles and between sexes. The burden of disabling conditions has serious implications for health system planning and health-related expenditures. Despite the progress made in reducing the burden of communicable diseases and neonatal disorders in low SDI countries, the speed of this progress could be increased by scaling up proven interventions. The global trends among non-communicable diseases indicate that more effort is needed to maximise HALE, such as risk prevention and attention to upstream determinants of health. Copyright © 2018 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license.
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    Global, regional, and national incidence, prevalence, and years lived with disability for 328 diseases and injuries for 195 countries, 1990-2016: A systematic analysis for the Global Burden of Disease Study 2016
    (2017)
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    Yakob, Bereket (57203811497)
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    Yan, Lijing L. (35933756700)
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    Yano, Yuichiro (57196965200)
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    Ye, Pengpeng (57202839295)
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    Yimam, Hassen Hamid (57196325590)
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    Yip, Paul (7102503720)
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    Yonemoto, Naohiro (57204947657)
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    Yoon, Seok-Jun (24823148900)
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    Yotebieng, Marcel (26325950800)
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    Younis, Mustafa Z. (8549393000)
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    Zaidi, Zoubida (57197376721)
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    Zaki, Maysaa El Sayed (57203666922)
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    Zegeye, Elias Asfaw (57209171278)
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    Zenebe, Zerihun Menlkalew (57200737185)
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    Zhang, Xueying (56283378700)
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    Zhou, Maigeng (57054557200)
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    Zipkin, Ben (57200737130)
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    Zodpey, Sanjay (7003415080)
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    Zuhlke, Liesl Joanna (57209027746)
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    Murray, Christopher J.L. (55481130700)
    Background As mortality rates decline, life expectancy increases, and populations age, non-fatal outcomes of diseases and injuries are becoming a larger component of the global burden of disease. The Global Burden of Diseases, Injuries, and Risk Factors Study 2016 (GBD 2016) provides a comprehensive assessment of prevalence, incidence, and years lived with disability (YLDs) for 328 causes in 195 countries and territories from 1990 to 2016. Methods We estimated prevalence and incidence for 328 diseases and injuries and 2982 sequelae, their non-fatal consequences. We used DisMod-MR 2.1, a Bayesian meta-regression tool, as the main method of estimation, ensuring consistency between incidence, prevalence, remission, and cause of death rates for each condition. For some causes, we used alternative modelling strategies if incidence or prevalence needed to be derived from other data. YLDs were estimated as the product of prevalence and a disability weight for all mutually exclusive sequelae, corrected for comorbidity and aggregated to cause level. We updated the Socio-demographic Index (SDI), a summary indicator of income per capita, years of schooling, and total fertility rate. GBD 2016 complies with the Guidelines for Accurate and Transparent Health Estimates Reporting (GATHER). Findings Globally, low back pain, migraine, age-related and other hearing loss, iron-deficiency anaemia, and major depressive disorder were the five leading causes of YLDs in 2016, contributing 57·6 million (95% uncertainty interval [UI] 40·8-75·9 million [7·2%, 6·0-8·3]), 45·1 million (29·0-62·8 million [5·6%, 4·0-7·2]), 36·3 million (25·3-50·9 million [4·5%, 3·8-5·3]), 34·7 million (23·0-49·6 million [4·3%, 3·5-5·2]), and 34·1 million (23·5-46·0 million [4·2%, 3·2-5·3]) of total YLDs, respectively. Age-standardised rates of YLDs for all causes combined decreased between 1990 and 2016 by 2·7% (95% UI 2·3-3·1). Despite mostly stagnant age-standardised rates, the absolute number of YLDs from non-communicable diseases has been growing rapidly across all SDI quintiles, partly because of population growth, but also the ageing of populations. The largest absolute increases in total numbers of YLDs globally were between the ages of 40 and 69 years. Age-standardised YLD rates for all conditions combined were 10·4% (95% UI 9·0-11·8) higher in women than in men. Iron-deficiency anaemia, migraine, Alzheimer's disease and other dementias, major depressive disorder, anxiety, and all musculoskeletal disorders apart from gout were the main conditions contributing to higher YLD rates in women. Men had higher age-standardised rates of substance use disorders, diabetes, cardiovascular diseases, cancers, and all injuries apart from sexual violence. Globally, we noted much less geographical variation in disability than has been documented for premature mortality. In 2016, there was a less than two times difference in age-standardised YLD rates for all causes between the location with the lowest rate (China, 9201 YLDs per 100 000, 95% UI 6862-11943) and highest rate (Yemen, 14 774 YLDs per 100 000, 11 018-19 228). Interpretation The decrease in death rates since 1990 for most causes has not been matched by a similar decline in age-standardised YLD rates. For many large causes, YLD rates have either been stagnant or have increased for some causes, such as diabetes. As populations are ageing, and the prevalence of disabling disease generally increases steeply with age, health systems will face increasing demand for services that are generally costlier than the interventions that have led to declines in mortality in childhood or for the major causes of mortality in adults. Up-todate information about the trends of disease and how this varies between countries is essential to plan for an adequate health-system response. © The Author(s). Published by Elsevier Ltd.
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    Publication
    Global, regional, and national incidence, prevalence, and years lived with disability for 354 Diseases and Injuries for 195 countries and territories, 1990-2017: A systematic analysis for the Global Burden of Disease Study 2017
    (2018)
    James, Spencer L. (57202557998)
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    Abate, Degu (57204237665)
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    Abate, Kalkidan Hassen (57207943858)
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    Abay, Solomon M. (35306466900)
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    Abbafati, Cristiana (54917122400)
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    Abbasi, Nooshin (57212442022)
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    Abbastabar, Hedayat (57212441848)
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    Abd-Allah, Foad (36503428900)
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    Abdela, Jemal (57200613000)
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    Abdelalim, Ahmed (7801307783)
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    Abdollahpour, Ibrahim (36997151900)
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    Abdulkader, Rizwan Suliankatchi (57195295816)
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    Abebe, Zegeye (57193002719)
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    Abil, Olifan Zewdie (57204558002)
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    Abraha, Haftom Niguse (57195289877)
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    Abu-Rmeileh, Niveen M.E. (57216675148)
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    Accrombessi, Manfred Mario Kokou (55353650500)
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    Srinivasan, Vinay (57196077031)
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    Stanaway, Jeffrey D. (57201210928)
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    Stein, Dan J. (55769747595)
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    Steiner, Caitlyn (57205358084)
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    Steiner, Timothy J. (16837503200)
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    Stokes, Mark A. (7102859000)
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    Stovner, Lars Jacob (57201788390)
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    Subart, Michelle L. (57194140438)
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    Sudaryanto, Agus (57305372500)
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    Sufiyan, Mu'awiyyah Babale (58294633600)
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    Sunguya, Bruno F. (57209060557)
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    Sur, Patrick John (57218360398)
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    Sykes, Bryan L. (57211183396)
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    Sylte, Dillon O. (57211183601)
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    Tabarés-Seisdedos, Rafael (6602981102)
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    Tadakamadla, Santosh Kumar (57207799926)
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    Tadesse, Birkneh Tilahun (56811144600)
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    Tandon, Nikhil (7101833756)
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    Tassew, Segen Gebremeskel (57204569108)
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    Tavakkoli, Mohammad (57202524239)
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    Taveira, Nuno (6602731390)
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    Taylor, Hugh R. (55550572900)
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    Tehrani-Banihashemi, Arash (57204006020)
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    Tekalign, Tigist Gashaw (57204558037)
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    Tekelemedhin, Shishay Wahdey (57204566273)
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    Tekle, Merhawi Gebremedhin (57204237146)
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    Temesgen, Habtamu (57205011874)
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    Temsah, Mohamad-Hani (56115852000)
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    Temsah, Omar (57204559820)
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    Terkawi, Abdullah Sulieman (57211144258)
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    Teweldemedhin, Mebrahtu (57193667629)
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    Thankappan, Kavumpurathu Raman (57202955435)
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    Thomas, Nihal (7401830494)
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    Tilahun, Binyam (57212075730)
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    To, Quyen G. (55827789100)
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    Tonelli, Marcello (7103102534)
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    Topor-Madry, Roman (57211182892)
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    Topouzis, Fotis (57194262710)
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    Torre, Anna E. (57196074351)
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    Tortajada-Girbés, Miguel (16242320900)
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    Touvier, Mathilde (8877033300)
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    Tovani-Palone, Marcos Roberto (56644977900)
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    Towbin, Jeffrey A. (7102520568)
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    Tran, Bach Xuan (57209107515)
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    Tran, Khanh Bao (57201651536)
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    Troeger, Christopher E. (57195223624)
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    Unutzer, Jurgen (7007005108)
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    Venketasubramanian, Narayanaswamy (56804702100)
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    Villafaina, Santos (57195804127)
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    Violante, Francesco S. (7003555890)
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    Vladimirov, Sergey Konstantinovitch (57195959162)
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    Waller, Stephen G. (57201445180)
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    Wang, Yafeng (57208674780)
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    Yahyazadeh Jabbari, Seyed Hossein (26029029100)
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    Yamada, Tomohide (37662679800)
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    Yan, Lijing L. (57198311895)
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    Yano, Yuichiro (57196965200)
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    Yaseri, Mehdi (23029507000)
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    Yasin, Yasin Jemal (57204565144)
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    Yeshaneh, Alex (57204564144)
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    Yimer, Ebrahim M. (57202256312)
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    Yip, Paul (7102503720)
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    Yonemoto, Naohiro (57204947657)
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    Yoon, Seok-Jun (24823148900)
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    Yotebieng, Marcel (26325950800)
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    Yousefifard, Mahmoud (57204566585)
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    Yu, Chuanhua (57208140344)
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    Zadnik, Vesna (57202975428)
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    Zaman, Sojib Bin (57193070058)
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    Zamani, Mohammad (59866744200)
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    Zare, Zohreh (35436578700)
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    Zeleke, Ayalew Jejaw (57193096860)
    Background: The Global Burden of Diseases, Injuries, and Risk Factors Study 2017 (GBD 2017) includes a comprehensive assessment of incidence, prevalence, and years lived with disability (YLDs) for 354 causes in 195 countries and territories from 1990 to 2017. Previous GBD studies have shown how the decline of mortality rates from 1990 to 2016 has led to an increase in life expectancy, an ageing global population, and an expansion of the non-fatal burden of disease and injury. These studies have also shown how a substantial portion of the world's population experiences non-fatal health loss with considerable heterogeneity among different causes, locations, ages, and sexes. Ongoing objectives of the GBD study include increasing the level of estimation detail, improving analytical strategies, and increasing the amount of high-quality data. Methods: We estimated incidence and prevalence for 354 diseases and injuries and 3484 sequelae. We used an updated and extensive body of literature studies, survey data, surveillance data, inpatient admission records, outpatient visit records, and health insurance claims, and additionally used results from cause of death models to inform estimates using a total of 68 781 data sources. Newly available clinical data from India, Iran, Japan, Jordan, Nepal, China, Brazil, Norway, and Italy were incorporated, as well as updated claims data from the USA and new claims data from Taiwan (province of China) and Singapore. We used DisMod-MR 2.1, a Bayesian meta-regression tool, as the main method of estimation, ensuring consistency between rates of incidence, prevalence, remission, and cause of death for each condition. YLDs were estimated as the product of a prevalence estimate and a disability weight for health states of each mutually exclusive sequela, adjusted for comorbidity. We updated the Socio-demographic Index (SDI), a summary development indicator of income per capita, years of schooling, and total fertility rate. Additionally, we calculated differences between male and female YLDs to identify divergent trends across sexes. GBD 2017 complies with the Guidelines for Accurate and Transparent Health Estimates Reporting. Findings: Globally, for females, the causes with the greatest age-standardised prevalence were oral disorders, headache disorders, and haemoglobinopathies and haemolytic anaemias in both 1990 and 2017. For males, the causes with the greatest age-standardised prevalence were oral disorders, headache disorders, and tuberculosis including latent tuberculosis infection in both 1990 and 2017. In terms of YLDs, low back pain, headache disorders, and dietary iron deficiency were the leading Level 3 causes of YLD counts in 1990, whereas low back pain, headache disorders, and depressive disorders were the leading causes in 2017 for both sexes combined. All-cause age-standardised YLD rates decreased by 3·9% (95% uncertainty interval [UI] 3·1-4·6) from 1990 to 2017; however, the all-age YLD rate increased by 7·2% (6·0-8·4) while the total sum of global YLDs increased from 562 million (421-723) to 853 million (642-1100). The increases for males and females were similar, with increases in all-age YLD rates of 7·9% (6·6-9·2) for males and 6·5% (5·4-7·7) for females. We found significant differences between males and females in terms of age-standardised prevalence estimates for multiple causes. The causes with the greatest relative differences between sexes in 2017 included substance use disorders (3018 cases [95% UI 2782-3252] per 100 000 in males vs 1400 [1279-1524] per 100 000 in females), transport injuries (3322 [3082-3583] vs 2336 [2154-2535]), and self-harm and interpersonal violence (3265 [2943-3630] vs 5643 [5057-6302]). Interpretation: Global all-cause age-standardised YLD rates have improved only slightly over a period spanning nearly three decades. However, the magnitude of the non-fatal disease burden has expanded globally, with increasing numbers of people who have a wide spectrum of conditions. A subset of conditions has remained globally pervasive since 1990, whereas other conditions have displayed more dynamic trends, with different ages, sexes, and geographies across the globe experiencing varying burdens and trends of health loss. This study emphasises how global improvements in premature mortality for select conditions have led to older populations with complex and potentially expensive diseases, yet also highlights global achievements in certain domains of disease and injury. Copyright © 2018 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license.
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    Global, regional, and national under-5 mortality, adult mortality, age-specific mortality, and life expectancy, 1970-2016: A systematic analysis for the Global Burden of Disease Study 2016
    (2017)
    Wang, Haidong (16507828100)
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    Abajobir, Amanuel Alemu (57203613441)
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    Abate, Kalkidan Hassen (57207943858)
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    Abbas, Kaja M. (57190285707)
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    Abera, Semaw Ferede (57205180598)
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    Abraha, Haftom Niguse (57195289877)
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    Bell, Michelle L. (7401466450)
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    Fereshtehnejad, Seyed-Mohammad (57202557520)
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    Fernandes, Jefferson G. (57220736619)
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    Fernandes, João C. (35274726800)
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    Feyissa, Tesfaye Regassa (57222562476)
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    Islam, Sheikh Mohammed Shariful (56400111100)
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    Shetty, Balakrishna P. (57194580871)
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    Shrime, Mark G. (57204703404)
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    Silveira, Dayane Gabriele Alves (57190284103)
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    Singh, Abhishek (59639211800)
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    Sreeramareddy, Chandrashekhar T. (57212263335)
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    Srinivasan, Vinay (57196077031)
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    Strong, Mark (12783473200)
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    Sufiyan, Muawiyyah Babale (58294633600)
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    Suliankatchi, Rizwan Abdulkader (57195295816)
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    Sunguya, Bruno F. (57209060557)
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    Swaminathan, Soumya (7102380757)
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    Zhang, Xueying (56283378700)
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    Murray, Christopher J.L. (55481130700)
    Background: Detailed assessments of mortality patterns, particularly age-specific mortality, represent a crucial input that enables health systems to target interventions to specific populations. Understanding how all-cause mortality has changed with respect to development status can identify exemplars for best practice. To accomplish this, the Global Burden of Diseases, Injuries, and Risk Factors Study 2016 (GBD 2016) estimated age-specific and sex-specific all-cause mortality between 1970 and 2016 for 195 countries and territories and at the subnational level for the five countries with a population greater than 200 million in 2016. Methods: We have evaluated how well civil registration systems captured deaths using a set of demographic methods called death distribution methods for adults and from consideration of survey and census data for children younger than 5 years. We generated an overall assessment of completeness of registration of deaths by dividing registered deaths in each location-year by our estimate of all-age deaths generated from our overall estimation process. For 163 locations, including subnational units in countries with a population greater than 200 million with complete vital registration (VR) systems, our estimates were largely driven by the observed data, with corrections for small fluctuations in numbers and estimation for recent years where there were lags in data reporting (lags were variable by location, generally between 1 year and 6 years). For other locations, we took advantage of different data sources available to measure under-5 mortality rates (U5MR) using complete birth histories, summary birth histories, and incomplete VR with adjustments; we measured adult mortality rate (the probability of death in individuals aged 15-60 years) using adjusted incomplete VR, sibling histories, and household death recall. We used the U5MR and adult mortality rate, together with crude death rate due to HIV in the GBD model life table system, to estimate age-specific and sex-specific death rates for each location-year. Using various international databases, we identified fatal discontinuities, which we defined as increases in the death rate of more than one death per million, resulting from conflict and terrorism, natural disasters, major transport or technological accidents, and a subset of epidemic infectious diseases; these were added to estimates in the relevant years. In 47 countries with an identified peak adult prevalence for HIV/AIDS of more than 0.5% and where VR systems were less than 65% complete, we informed our estimates of age-sex-specific mortality using the Estimation and Projection Package (EPP)-Spectrum model fitted to national HIV/AIDS prevalence surveys and antenatal clinic serosurveillance systems. We estimated stillbirths, early neonatal, late neonatal, and childhood mortality using both survey and VR data in spatiotemporal Gaussian process regression models. We estimated abridged life tables for all location-years using age-specific death rates. We grouped locations into development quintiles based on the Socio-demographic Index (SDI) and analysed mortality trends by quintile. Using spline regression, we estimated the expected mortality rate for each age-sex group as a function of SDI. We identified countries with higher life expectancy than expected by comparing observed life expectancy to anticipated life expectancy on the basis of development status alone. Findings: Completeness in the registration of deaths increased from 28% in 1970 to a peak of 45% in 2013; completeness was lower after 2013 because of lags in reporting. Total deaths in children younger than 5 years decreased from 1970 to 2016, and slower decreases occurred at ages 5-24 years. By contrast, numbers of adult deaths increased in each 5-year age bracket above the age of 25 years. The distribution of annualised rates of change in age-specific mortality rate differed over the period 2000 to 2016 compared with earlier decades: increasing annualised rates of change were less frequent, although rising annualised rates of change still occurred in some locations, particularly for adolescent and younger adult age groups. Rates of stillbirths and under-5 mortality both decreased globally from 1970. Evidence for global convergence of death rates was mixed; although the absolute difference between age-standardised death rates narrowed between countries at the lowest and highest levels of SDI, the ratio of these death rates - a measure of relative inequality - increased slightly. There was a strong shift between 1970 and 2016 toward higher life expectancy, most noticeably at higher levels of SDI. Among countries with populations greater than 1 million in 2016, life expectancy at birth was highest for women in Japan, at 86.9 years (95% UI 86.7-87.2), and for men in Singapore, at 81.3 years (78.8-83.7) in 2016. Male life expectancy was generally lower than female life expectancy between 1970 and 2016, and the gap between male and female life expectancy increased with progression to higher levels of SDI. Some countries with exceptional health performance in 1990 in terms of the difference in observed to expected life expectancy at birth had slower progress on the same measure in 2016. Interpretation Globally, mortality rates have decreased across all age groups over the past five decades, with the largest improvements occurring among children younger than 5 years. However, at the national level, considerable heterogeneity remains in terms of both level and rate of changes in age-specific mortality; increases in mortality for certain age groups occurred in some locations. We found evidence that the absolute gap between countries in age-specific death rates has declined, although the relative gap for some age-sex groups increased. Countries that now lead in terms of having higher observed life expectancy than that expected on the basis of development alone, or locations that have either increased this advantage or rapidly decreased the deficit from expected levels, could provide insight into the means to accelerate progress in nations where progress has stalled. Copyright © The Author(s).
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