Browsing by Author "Miličić, Tanja (24073432600)"
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Publication Altered daytime fluctuation pattern of plasminogen activator inhibitor 1 in type 2 diabetes patients with coronary artery disease: A strong association with persistently elevated plasma insulin, increased insulin resistance, and abdominal obesity(2015) ;Lalić, Katarina (13702563300) ;Jotić, Aleksandra (13702545200) ;Rajković, Nataša (13702670500) ;Singh, Sandra (16022873000) ;Stošić, Ljubica (57205884711) ;Popović, Ljiljana (7004316275) ;Lukić, Ljiljana (24073403700) ;Miličić, Tanja (24073432600) ;Seferović, Jelena P. (23486982900) ;Maćešić, Marija (26967836100) ;Stanarčić, Jelena (59663037000) ;Čivčić, Milorad (18436145000) ;Kadić, Iva (56674542000)Lalić, Nebojša M. (13702597500)This study was aimed at investigating daily fluctuation of PAI-1 levels in relation to insulin resistance (IR) and daily profile of plasma insulin and glucose levels in 26 type 2 diabetic (T2D) patients with coronary artery disease (CAD) (group A), 10 T2D patients without CAD (group B), 12 nondiabetics with CAD (group C), and 12 healthy controls (group D). The percentage of PAI-1 decrease was lower in group A versus group B (4.4 ± 2.7 versus 35.0 ± 5.4%; P<0.05) and in C versus D (14.0 ± 5.8 versus 44.7 ± 3.1%; P<0.001). HOMA-IR was higher in group A versus group B (P<0.05) and in C versus D (P<0.01). Simultaneously, AUCs of PAI-1 and insulin were higher in group A versus group B (P<0.05) and in C versus D (P<0.01), while AUC of glucose did not differ between groups. In multiple regression analysis waist-to-hip ratio and AUC of insulin were independent determinants of decrease in PAI-1. The altered diurnal fluctuation of PAI-1, especially in T2D with CAD, might be strongly influenced by a prolonged exposure to hyperinsulinemia in the settings of increased IR and abdominal obesity, facilitating altogether an accelerated atherosclerosis. © 2015 Katarina Lalić et al. - Some of the metrics are blocked by yourconsent settings
Publication Altered daytime fluctuation pattern of plasminogen activator inhibitor 1 in type 2 diabetes patients with coronary artery disease: A strong association with persistently elevated plasma insulin, increased insulin resistance, and abdominal obesity(2015) ;Lalić, Katarina (13702563300) ;Jotić, Aleksandra (13702545200) ;Rajković, Nataša (13702670500) ;Singh, Sandra (16022873000) ;Stošić, Ljubica (57205884711) ;Popović, Ljiljana (7004316275) ;Lukić, Ljiljana (24073403700) ;Miličić, Tanja (24073432600) ;Seferović, Jelena P. (23486982900) ;Maćešić, Marija (26967836100) ;Stanarčić, Jelena (59663037000) ;Čivčić, Milorad (18436145000) ;Kadić, Iva (56674542000)Lalić, Nebojša M. (13702597500)This study was aimed at investigating daily fluctuation of PAI-1 levels in relation to insulin resistance (IR) and daily profile of plasma insulin and glucose levels in 26 type 2 diabetic (T2D) patients with coronary artery disease (CAD) (group A), 10 T2D patients without CAD (group B), 12 nondiabetics with CAD (group C), and 12 healthy controls (group D). The percentage of PAI-1 decrease was lower in group A versus group B (4.4 ± 2.7 versus 35.0 ± 5.4%; P<0.05) and in C versus D (14.0 ± 5.8 versus 44.7 ± 3.1%; P<0.001). HOMA-IR was higher in group A versus group B (P<0.05) and in C versus D (P<0.01). Simultaneously, AUCs of PAI-1 and insulin were higher in group A versus group B (P<0.05) and in C versus D (P<0.01), while AUC of glucose did not differ between groups. In multiple regression analysis waist-to-hip ratio and AUC of insulin were independent determinants of decrease in PAI-1. The altered diurnal fluctuation of PAI-1, especially in T2D with CAD, might be strongly influenced by a prolonged exposure to hyperinsulinemia in the settings of increased IR and abdominal obesity, facilitating altogether an accelerated atherosclerosis. © 2015 Katarina Lalić et al. - Some of the metrics are blocked by yourconsent settings
Publication Asymptomatic cardiovascular manifestations in diabetes mellitus: Left ventricular diastolic dysfunction and silent myocardial ischemia(2011) ;Seferović-Mitrović, Jelena P. (23486982900) ;Lalić, Nebojša M. (13702597500) ;Vujisić-Tešić, Bosiljka (6508177183) ;Lalić, Katarina (13702563300) ;Jotić, Aleksandra (13702545200) ;Ristić, Arsen D. (7003835406) ;Giga, Vojislav (55924460200) ;Tešić, Milorad (36197477200) ;Milić, Nataša (7003460927) ;Lukić, Ljiljana (24073403700) ;Miličić, Tanja (24073432600) ;Singh, Sandra (16022873000)Seferović, Petar M. (6603594879)Introduction Several cardiovascular manifestations in patients with diabetes may be asymptomatic. Left ventricular diastolic dysfunction (LVDD) is considered to be the earliest metabolic myocardial lesion in these patients, and can be diagnosed with tissue Doppler echocardiography. Silent myocardial ischemia (SMI) is a characteristic and frequently described form of ischemic heart disease in patients with diabetes. Objective The aim of the study was to assess the prevalence of LVDD and SMI in patients with type 2 diabetes, as well as to compare demographic, clinical, and metabolic data among defined groups (patients with LVDD, patients with SMI and patients with type 2 diabetes, without LVDD and SMI). Methods We investigated 104 type 2 diabetic patients (mean age 55.4±9.1 years, 64.4% males) with normal blood pressure, prehypertension and arterial hypertension stage I. Study design included basic laboratory assessment and cardiological workup (transthoracic echocardiography and tissue Doppler as well as the exercise stress echocardiography). Results LVDD was diagnosed in twelve patients (11.5%), while SMI was revealed in six patients (5.8%). Less patients with LVDD were using metformin, in comparison to other two groups (χ2 =12.152; p=0.002). Values of HDL cholesterol (F=4.515; p=0.013) and apolipoprotein A1 (F=5.128; p= 0.008) were significantly higher in patients with LVDD. Conclusion The study confirmed asymptomatic cardiovascular complications in 17.3% patients with type 2 diabetes. - Some of the metrics are blocked by yourconsent settings
Publication Corticosteroid treatment and growth of angiolipomas in patient with two rare diseases: Pfeifer–Weber–Christian disease and benign multiple subcutaneous angiolipomas(2023) ;Radunović, Goran (13402761800) ;Miličić, Tanja (24073432600) ;Bosić, Martina (56606207600) ;Jeremić, Ivan (36016708800) ;Dačić, Draško (57787613600)Pavlov-Dolijanović, Slavica (8452470400)SUMMARY Introduction Pfeifer–Weber–Christian disease (PWCD) is a rare inflammatory disorder of the subcutaneous fatty tissue. Angiolipoma, is a benign adipocytic soft tissue tumor composed of mature adipose tissue and small vascular proliferations. Treatment with corticosteroids could lead to proliferation of fat tissue but the stimulation of angiolipoma growth during corticosteroid therapy is extremely rare. Case outline We describe a case of a 46-year-old female patient with histopathological confirmation two rare diseases: PWCD and benign multiple subcutaneous non-infiltrative angiolipomas. Angiolipo-mas were treated conservatively. Treatment for PWCD was prednisone 20 mg/day. Due to poor control of PWCD and rapid angiolipomas growth on forearms, corticosteroids were discontinued after two months of use. Administration of oral cyclosporine A led to a rapid remission of the PWCD, and with no new growth of angiolipomas. Conclusion The successful therapy with the Cyclosporine A supports the hypothesis that PWCD is a T cell mediated autoinflammatory condition. Rapid growth of angiolipoma during corticosteroid therapy is an extremely rare condition. © 2023, Serbia Medical Society. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Endothelial dysfunction of coronary arteries in subjects without diabetes: An association with both insulin resistance and impaired insulin secretion response(2018) ;Lalić, Katarina (13702563300) ;Nedeljković, Milan (7004488186) ;Jotić, Alekasandra (13702545200) ;Babić, Rade (16165040200) ;Rajković, Nataša (13702670500) ;Popović, Ljiljana (7004316275) ;Lukić, Ljiljana (24073403700) ;Miličić, Tanja (24073432600) ;Singh Lukač, Sandra (16022873000) ;Stošić, Ljubica (57205884711) ;Maćešić, Marija (26967836100) ;Rasulić, Iva (57201359522) ;Gajović, Jelena Stanarčić (56089716900)Lalić, Nebojša M. (13702597500)Aims: This study was aimed to compare insulin sensitivity and secretion response, lipoprotein and plasminogen activator inhibitor 1 (PAI-1) levels between the subjects with and without coronary artery endothelial dysfunction (ED). Methods: ED was detected by intracoronary injection of acetylcholine (ACh) in 47 nondiabetes subjects without stenotic coronary arteries, selected from 316 consecutive patients with coronary angiography performed for suspected coronary artery disease. The subjects were divided into two groups: presence of ACh-induced coronary spasm (group ED+, N = 30) and absence of ACh-induced coronary spasm (group ED− N = 17). Insulin sensitivity (Si) was evaluated by frequently sampled intravenous glucose tolerance test (FSIGTT) with minimal model analysis and by HOMA-IR, insulin secretion by acute insulin response (AIR) (calculated from the first 8 min of FSIGTT) and by disposition index (DI) (Si × AIR). Lipids and PAI-1 levels were determined enzymatically, and LDL particle size by gradient gel electrophoresis. Results: Si was significantly lower (4.22 ± 0.62 vs 6.98 ± 1.47 min−1/mU/l × 104; p < 0.05) while HOMA-IR was significantly higher in ED + group vs ED− group (2.8 ± 0.3 vs 1.7 ± 0.2; p < 0.05). Simultaneously, AIR and DI was significantly lower in ED + vs ED− groups (p < 0.05 and p < 0.01, respectively). Investigated groups did not differ in fasting lipid levels but ED+ group had significantly smaller LDL particles (p < 0.01) and higher PAI-1 levels (p < 0.05). Regression analysis shown that DI was a strong independent predictor of appearance of ED, together with PAI-1 and LDL particle size. Conclusions: Both insulin resistance and impairment in insulin secretion response strongly correlate with coronary ED in subjects without diabetes. © 2018 Elsevier B.V. - Some of the metrics are blocked by yourconsent settings
Publication Endothelial dysfunction of coronary arteries in subjects without diabetes: An association with both insulin resistance and impaired insulin secretion response(2018) ;Lalić, Katarina (13702563300) ;Nedeljković, Milan (7004488186) ;Jotić, Alekasandra (13702545200) ;Babić, Rade (16165040200) ;Rajković, Nataša (13702670500) ;Popović, Ljiljana (7004316275) ;Lukić, Ljiljana (24073403700) ;Miličić, Tanja (24073432600) ;Singh Lukač, Sandra (16022873000) ;Stošić, Ljubica (57205884711) ;Maćešić, Marija (26967836100) ;Rasulić, Iva (57201359522) ;Gajović, Jelena Stanarčić (56089716900)Lalić, Nebojša M. (13702597500)Aims: This study was aimed to compare insulin sensitivity and secretion response, lipoprotein and plasminogen activator inhibitor 1 (PAI-1) levels between the subjects with and without coronary artery endothelial dysfunction (ED). Methods: ED was detected by intracoronary injection of acetylcholine (ACh) in 47 nondiabetes subjects without stenotic coronary arteries, selected from 316 consecutive patients with coronary angiography performed for suspected coronary artery disease. The subjects were divided into two groups: presence of ACh-induced coronary spasm (group ED+, N = 30) and absence of ACh-induced coronary spasm (group ED− N = 17). Insulin sensitivity (Si) was evaluated by frequently sampled intravenous glucose tolerance test (FSIGTT) with minimal model analysis and by HOMA-IR, insulin secretion by acute insulin response (AIR) (calculated from the first 8 min of FSIGTT) and by disposition index (DI) (Si × AIR). Lipids and PAI-1 levels were determined enzymatically, and LDL particle size by gradient gel electrophoresis. Results: Si was significantly lower (4.22 ± 0.62 vs 6.98 ± 1.47 min−1/mU/l × 104; p < 0.05) while HOMA-IR was significantly higher in ED + group vs ED− group (2.8 ± 0.3 vs 1.7 ± 0.2; p < 0.05). Simultaneously, AIR and DI was significantly lower in ED + vs ED− groups (p < 0.05 and p < 0.01, respectively). Investigated groups did not differ in fasting lipid levels but ED+ group had significantly smaller LDL particles (p < 0.01) and higher PAI-1 levels (p < 0.05). Regression analysis shown that DI was a strong independent predictor of appearance of ED, together with PAI-1 and LDL particle size. Conclusions: Both insulin resistance and impairment in insulin secretion response strongly correlate with coronary ED in subjects without diabetes. © 2018 Elsevier B.V. - Some of the metrics are blocked by yourconsent settings
Publication Glucose lowering drug or strategy dependent impact of weight reduction on the prevention of CVD outcomes in Type 2 diabetes: a systematic review of CVOTs(2024) ;Lalić, Nebojša M. (13702597500) ;Jotić, Aleksandra (13702545200) ;Lukić, Ljiljana (24073403700) ;Miličić, Tanja (24073432600) ;Maćešić, Marija (26967836100) ;Stanarčić Gajović, Jelena (56089716900) ;Stoiljković, Milica (57215024953) ;Milovančević, Mina (57236937100) ;Rafailović Cvetković, Djurdja (59278760500)Lalić, Katarina (13702563300)Aims: This systematic review was aimed to assess the association between magnitude of body weight loss (BWL) in type 2 diabetes (T2D) patients and cardiovascular (CV) risk in CV outcome trials (CVOTs). Methods: We searched electronic databases (PubMed, Cochrane and Scopus) for available CVOTs, observational cohort studies or post hoc analyses of clinical trials of adult T2D patients investigated the association of BWL with CV outcomes and/or all-cause mortality. Results: 19 RCTs of novel glucose-lowering drugs (GLP-1RA, DPP-4i and SGLT2i) and 6 RCT or observational trial of different strategies (intensive treatment or standard care) were included (379.904 T2D patients). Higher BWL during GLP-1RA treatment, in comaprison to lower BWL, was associated with higher decrease in risk of MACE, while DPP-4i had not that effect. With SGLT2i the higher decrease in risk of MACE was associated with lower BWL. In contrast, in other different strategies, higher BWL lead to increase in risk for MACE and all-cause mortality. Conclusions: In CVOTs, treatment of T2D patients resulted in BWL, which correlated with reduction in risk for CV outcomes, particularly with GLP-1 RAs. However, interventional non-CVOTs are warning that in the absence of structured behavioral intervention and relevant medication, the large BWL might be harmful for CV outcomes. © 2024 Elsevier B.V. - Some of the metrics are blocked by yourconsent settings
Publication Glucose lowering drug or strategy dependent impact of weight reduction on the prevention of CVD outcomes in Type 2 diabetes: a systematic review of CVOTs(2024) ;Lalić, Nebojša M. (13702597500) ;Jotić, Aleksandra (13702545200) ;Lukić, Ljiljana (24073403700) ;Miličić, Tanja (24073432600) ;Maćešić, Marija (26967836100) ;Stanarčić Gajović, Jelena (56089716900) ;Stoiljković, Milica (57215024953) ;Milovančević, Mina (57236937100) ;Rafailović Cvetković, Djurdja (59278760500)Lalić, Katarina (13702563300)Aims: This systematic review was aimed to assess the association between magnitude of body weight loss (BWL) in type 2 diabetes (T2D) patients and cardiovascular (CV) risk in CV outcome trials (CVOTs). Methods: We searched electronic databases (PubMed, Cochrane and Scopus) for available CVOTs, observational cohort studies or post hoc analyses of clinical trials of adult T2D patients investigated the association of BWL with CV outcomes and/or all-cause mortality. Results: 19 RCTs of novel glucose-lowering drugs (GLP-1RA, DPP-4i and SGLT2i) and 6 RCT or observational trial of different strategies (intensive treatment or standard care) were included (379.904 T2D patients). Higher BWL during GLP-1RA treatment, in comaprison to lower BWL, was associated with higher decrease in risk of MACE, while DPP-4i had not that effect. With SGLT2i the higher decrease in risk of MACE was associated with lower BWL. In contrast, in other different strategies, higher BWL lead to increase in risk for MACE and all-cause mortality. Conclusions: In CVOTs, treatment of T2D patients resulted in BWL, which correlated with reduction in risk for CV outcomes, particularly with GLP-1 RAs. However, interventional non-CVOTs are warning that in the absence of structured behavioral intervention and relevant medication, the large BWL might be harmful for CV outcomes. © 2024 Elsevier B.V.
