Browsing by Author "Marjanovic, Ivan (57201599576)"
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Publication Clinical and epidemiological features of Guillain-Barré syndrome in the Western Balkans(2014) ;Peric, Stojan (35750481700) ;Milosevic, Vuk (24480195100) ;Berisavac, Ivana (6507392420) ;Stojiljkovic, Olivera (56455361200) ;Beslac-Bumbasirevic, Ljiljana (6506489179) ;Marjanovic, Ivan (57201599576) ;Djuric, Vanja (35361619800) ;Djordjevic, Gordana (35763715800) ;Rajic, Sonja (56516616500) ;Cvijanovic, Milan (8208649800) ;Babic, Milica (56516407400) ;Dominovic, Aleksandra (56516864600) ;Vujovic, Balsa (57021631300) ;Cukic, Mirjana (55891936800) ;Petrovic, Milutin (36969833200) ;Toncev, Gordana (6506651230) ;Komatina, Nenad (56516845100) ;Martic, Vesna (6602650915)Lavrnic, Dragana (6602473221)The aim of this study was to define features of Guillain-Barré syndrome in a large cohort of patients from three Western Balkans countries. Data from adult Guillain-Barré syndrome (GBS) cases from 2009 to 2013 were retrospectively obtained from all tertiary health care centers. During the 5-year period, 327 new cases of GBS were identified with a male to female ratio of 1.7 : 1. The most common GBS variants were demyelinating (65%) and axonal (12%). At nadir 45% of patients were chair-bound, confined to bed, or required assisted ventilation, while 5% died. The crude incidence of GBS in Serbia and Montenegro was 0.93 per 100,000 population, and age-adjusted incidence according to the world standard population was 0.86 per 100,000. Incidence was particularly high in 50- to 80-year-old men. Statistically significant seasonal variations of GBS were not observed. This study of patients with GBS in the Western Balkans allows us to prepare the health system better and to improve the management of patients. This study also opens opportunities for international collaboration and for taking part in the multinational studies on GBS. © 2015 Peripheral Nerve Society. - Some of the metrics are blocked by yourconsent settings
Publication Clinical and epidemiological features of Guillain-Barré syndrome in the Western Balkans(2014) ;Peric, Stojan (35750481700) ;Milosevic, Vuk (24480195100) ;Berisavac, Ivana (6507392420) ;Stojiljkovic, Olivera (56455361200) ;Beslac-Bumbasirevic, Ljiljana (6506489179) ;Marjanovic, Ivan (57201599576) ;Djuric, Vanja (35361619800) ;Djordjevic, Gordana (35763715800) ;Rajic, Sonja (56516616500) ;Cvijanovic, Milan (8208649800) ;Babic, Milica (56516407400) ;Dominovic, Aleksandra (56516864600) ;Vujovic, Balsa (57021631300) ;Cukic, Mirjana (55891936800) ;Petrovic, Milutin (36969833200) ;Toncev, Gordana (6506651230) ;Komatina, Nenad (56516845100) ;Martic, Vesna (6602650915)Lavrnic, Dragana (6602473221)The aim of this study was to define features of Guillain-Barré syndrome in a large cohort of patients from three Western Balkans countries. Data from adult Guillain-Barré syndrome (GBS) cases from 2009 to 2013 were retrospectively obtained from all tertiary health care centers. During the 5-year period, 327 new cases of GBS were identified with a male to female ratio of 1.7 : 1. The most common GBS variants were demyelinating (65%) and axonal (12%). At nadir 45% of patients were chair-bound, confined to bed, or required assisted ventilation, while 5% died. The crude incidence of GBS in Serbia and Montenegro was 0.93 per 100,000 population, and age-adjusted incidence according to the world standard population was 0.86 per 100,000. Incidence was particularly high in 50- to 80-year-old men. Statistically significant seasonal variations of GBS were not observed. This study of patients with GBS in the Western Balkans allows us to prepare the health system better and to improve the management of patients. This study also opens opportunities for international collaboration and for taking part in the multinational studies on GBS. © 2015 Peripheral Nerve Society. - Some of the metrics are blocked by yourconsent settings
Publication COVID-19 infection and vaccination against SARS-CoV-2 in myasthenia gravis(2023) ;Peric, Stojan (35750481700) ;Rankovic, Milos (57942974000) ;Bozovic, Ivo (57194468421) ;Radosavljevic, Vanja (57942548800) ;Marjanovic, Ivan (57201599576) ;Basta, Ivana (8274374200)Lavrnic, Dragana (6602473221)Introduction: Myasthenia gravis (MG) is an autoimmune disease of the neuromuscular junction which is typically presented with muscle weakness and excessive fatigability. Majority of MG patients require long-term immune suppression. Our aim was to analyze the frequency and severity of COVID-19 infection in MG patients, as well as the frequency of vaccinated MG patients against SARS-CoV-2. Methods: We included 125 MG patients from the central Belgrade municipalities—60% females, age at MG onset 50.1 ± 19.7 years, age at testing 61.7 ± 16.8 years, anti-acetylcholine receptor (anti-AChR) positive 78% and muscle specific tyrosine kinase (MuSK) positive 8.6%. Results: One-third of our MG patients had a COVID-19 infection and they were younger compared to those without verified COVID-19. Severe COVID-19 infection was registered in 28% of MG patients, mostly in elder subjects with comorbidities such as cardiac diseases and malignancies. MG worsening was noted in 21% of patients during/after COVID-19 and 42% had COVID-19 sequelae. Majority of MG patients were vaccinated against SARS-CoV-2 (almost 70%). Vaccination was more common among MG patients with diabetes and in those with a milder form of MG. The most common types of vaccines were Sinopharm (42%) and Pfizer-BioNTech (25.6%). Adverse events were observed in 36% of vaccinated patients, with flu-like symptoms (77%) and local reactions (13%) being the most common ones. MG worsening was noticed in 5 (5.8%) patients after vaccination. Conclusion: COVID-19 has placed a significant new burden for MG patients. Elder MG patients and patients with comorbidities are in higher risk of having adverse outcome following SARS-CoV-2 infection. Percentage of vaccinated MG patients was higher than in general Serbian population. © 2022, The Author(s) under exclusive licence to Belgian Neurological Society. - Some of the metrics are blocked by yourconsent settings
Publication Proton magnetic resonance spectroscopy of the intrinsic tongue muscles in patients with myasthenia gravis with different autoantibodies(2011) ;Lavrnic, Dragana (6602473221) ;Dakovic, Marko (23491743200) ;Peric, Stojan (35750481700) ;Rakocevic-Stojanovic, Vidosava (6603893359) ;Basta, Ivana (8274374200) ;Marjanovic, Ivan (57201599576) ;Stosic-Opincal, Tatjana (55886486600)Lavrnic, Slobodan (23473613300)Objective: To assess lipid composition of the intrinsic tongue muscles in patients with myasthenia gravis (MG). Methods: This study included 15 MG patients with antibodies against muscle-specific kinase (MuSK), 15 matched MG patients with antibodies against acetylcholine receptor (AChR) and 15 matched healthy subjects. Middle posterior region of the tongue was analyzed by single voxel point-resolved proton magnetic resonance spectroscopy (MRS) using 1.5 T MRI scanner. Results: MRS obtained from subject with AChR MG showed a broad resonance arising from methylene groups of lipids (PMN) with no observable shoulder attributed to methyl groups (PML). Full-width at half maximum (FWHM) of PMN + PML peak showed higher value in patients with AChR MG in comparison to healthy subjects and MuSK MG patients (p < 0.05). In patients with MuSK MG, the shape and FWHM of PMN + PML peak was similar as in healthy subjects (p > 0.05), with tendency toward increased ratio between PMN and resonance from vinyl protons of lipids (PV). In both AChR and MuSK MG, total creatine resonance (creatine + phosphocreatine, CP) was almost absent with significant increase of PMN/CP ratio in comparison to healthy subjects (p < 0.05). Conclusion: MRS is useful in revealing muscle lipid composition in MG. In patients with AChR MG, MRS showed increased lipid content in the tongue muscles due to the lipid migration from intra- to extramyocellular space. Finding in patients with MuSK MG might reflect intramyocellular lipid deposition in the tongue. CP decrease in tongue muscles indicated impairment of oxidative metabolism in both AChR MG and MuSK MG. © 2010 Elsevier B.V. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Proton magnetic resonance spectroscopy of the intrinsic tongue muscles in patients with myasthenia gravis with different autoantibodies(2011) ;Lavrnic, Dragana (6602473221) ;Dakovic, Marko (23491743200) ;Peric, Stojan (35750481700) ;Rakocevic-Stojanovic, Vidosava (6603893359) ;Basta, Ivana (8274374200) ;Marjanovic, Ivan (57201599576) ;Stosic-Opincal, Tatjana (55886486600)Lavrnic, Slobodan (23473613300)Objective: To assess lipid composition of the intrinsic tongue muscles in patients with myasthenia gravis (MG). Methods: This study included 15 MG patients with antibodies against muscle-specific kinase (MuSK), 15 matched MG patients with antibodies against acetylcholine receptor (AChR) and 15 matched healthy subjects. Middle posterior region of the tongue was analyzed by single voxel point-resolved proton magnetic resonance spectroscopy (MRS) using 1.5 T MRI scanner. Results: MRS obtained from subject with AChR MG showed a broad resonance arising from methylene groups of lipids (PMN) with no observable shoulder attributed to methyl groups (PML). Full-width at half maximum (FWHM) of PMN + PML peak showed higher value in patients with AChR MG in comparison to healthy subjects and MuSK MG patients (p < 0.05). In patients with MuSK MG, the shape and FWHM of PMN + PML peak was similar as in healthy subjects (p > 0.05), with tendency toward increased ratio between PMN and resonance from vinyl protons of lipids (PV). In both AChR and MuSK MG, total creatine resonance (creatine + phosphocreatine, CP) was almost absent with significant increase of PMN/CP ratio in comparison to healthy subjects (p < 0.05). Conclusion: MRS is useful in revealing muscle lipid composition in MG. In patients with AChR MG, MRS showed increased lipid content in the tongue muscles due to the lipid migration from intra- to extramyocellular space. Finding in patients with MuSK MG might reflect intramyocellular lipid deposition in the tongue. CP decrease in tongue muscles indicated impairment of oxidative metabolism in both AChR MG and MuSK MG. © 2010 Elsevier B.V. All rights reserved.
