Prevalence and Impact of Nonalcoholic Fatty Liver Disease in Atrial Fibrillation

To estimate the prevalence of nonalcoholic fatty liver disease (NAFLD) and its impact on bleeding and thrombotic events in patients with atrial fibrillation (AF). Prospective multicenter cohort study including patients with nonvalvular AF receiving vitamin K antagonists (VKAs) or non-VKA oral antico...

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Veröffentlicht in:Mayo Clinic proceedings 2020-03, Vol.95 (3), p.513-520
Hauptverfasser: Pastori, Daniele, Sciacqua, Angela, Marcucci, Rossella, Farcomeni, Alessio, Perticone, Francesco, Del Ben, Maria, Angelico, Francesco, Baratta, Francesco, Pignatelli, Pasquale, Violi, Francesco, Saliola, Mirella, Santulli, Maria, Vasaturo, Fortunata, Casciaro, Marco Antonio, Cammisotto, Vittoria, Nocella, Cristina, Bartimoccia, Simona, Carnevale, Roberto, Iannilli, Claudia, Di Stefano, Tiziana, Iannucci, Patrizia, Sabbatini, Elio
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container_issue 3
container_start_page 513
container_title Mayo Clinic proceedings
container_volume 95
creator Pastori, Daniele
Sciacqua, Angela
Marcucci, Rossella
Farcomeni, Alessio
Perticone, Francesco
Del Ben, Maria
Angelico, Francesco
Baratta, Francesco
Pignatelli, Pasquale
Violi, Francesco
Saliola, Mirella
Santulli, Maria
Vasaturo, Fortunata
Casciaro, Marco Antonio
Cammisotto, Vittoria
Nocella, Cristina
Bartimoccia, Simona
Carnevale, Roberto
Iannilli, Claudia
Di Stefano, Tiziana
Iannucci, Patrizia
Sabbatini, Elio
description To estimate the prevalence of nonalcoholic fatty liver disease (NAFLD) and its impact on bleeding and thrombotic events in patients with atrial fibrillation (AF). Prospective multicenter cohort study including patients with nonvalvular AF receiving vitamin K antagonists (VKAs) or non-VKA oral anticoagulants (NOACs) from February 2008 for patients on VKA and from September 2013 for patients on NOACs. NAFLD was diagnosed using the validated fatty liver index, with a cutoff score of 60 or higher. Primary end points were the occurrence of major bleedings and cardiovascular events (CVEs). NAFLD was diagnosed in 732 of 1735 (42.2%) patients. Patients with NAFLD were younger, less frequently women, and more likely to be treated with NOACs and to have obesity, dyslipidemia, and persistent/permanent AF. During a median follow-up of 18.7 months (3155 patient-years), we recorded 78 major bleedings (incidence rate, 2.5% per year): 29 (2.1% per year) in patients with and 49 (2.7% per year) in patients without NAFLD (log-rank test P=.23). Univariate Cox proportional regression analysis showed no association of NAFLD with major bleedings (hazard ratio, 0.75; 95% CI, 0.47-1.20; P=.23). One hundred fifty-five CVEs occurred (incidence rate, 3.1% per year). No significant association was found between NAFLD and CVEs (log-rank test P=.12). In the entire population, NOAC use was associated with lower CVEs compared with VKAs (hazard ratio, 0.61; 95% CI, 0.42-0.89; P=.01). NAFLD is highly prevalent in AF but is not associated with higher bleeding or thrombotic risk.
doi_str_mv 10.1016/j.mayocp.2019.08.027
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Prospective multicenter cohort study including patients with nonvalvular AF receiving vitamin K antagonists (VKAs) or non-VKA oral anticoagulants (NOACs) from February 2008 for patients on VKA and from September 2013 for patients on NOACs. NAFLD was diagnosed using the validated fatty liver index, with a cutoff score of 60 or higher. Primary end points were the occurrence of major bleedings and cardiovascular events (CVEs). NAFLD was diagnosed in 732 of 1735 (42.2%) patients. Patients with NAFLD were younger, less frequently women, and more likely to be treated with NOACs and to have obesity, dyslipidemia, and persistent/permanent AF. During a median follow-up of 18.7 months (3155 patient-years), we recorded 78 major bleedings (incidence rate, 2.5% per year): 29 (2.1% per year) in patients with and 49 (2.7% per year) in patients without NAFLD (log-rank test P=.23). Univariate Cox proportional regression analysis showed no association of NAFLD with major bleedings (hazard ratio, 0.75; 95% CI, 0.47-1.20; P=.23). One hundred fifty-five CVEs occurred (incidence rate, 3.1% per year). No significant association was found between NAFLD and CVEs (log-rank test P=.12). In the entire population, NOAC use was associated with lower CVEs compared with VKAs (hazard ratio, 0.61; 95% CI, 0.42-0.89; P=.01). 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Prospective multicenter cohort study including patients with nonvalvular AF receiving vitamin K antagonists (VKAs) or non-VKA oral anticoagulants (NOACs) from February 2008 for patients on VKA and from September 2013 for patients on NOACs. NAFLD was diagnosed using the validated fatty liver index, with a cutoff score of 60 or higher. Primary end points were the occurrence of major bleedings and cardiovascular events (CVEs). NAFLD was diagnosed in 732 of 1735 (42.2%) patients. Patients with NAFLD were younger, less frequently women, and more likely to be treated with NOACs and to have obesity, dyslipidemia, and persistent/permanent AF. During a median follow-up of 18.7 months (3155 patient-years), we recorded 78 major bleedings (incidence rate, 2.5% per year): 29 (2.1% per year) in patients with and 49 (2.7% per year) in patients without NAFLD (log-rank test P=.23). 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Prospective multicenter cohort study including patients with nonvalvular AF receiving vitamin K antagonists (VKAs) or non-VKA oral anticoagulants (NOACs) from February 2008 for patients on VKA and from September 2013 for patients on NOACs. NAFLD was diagnosed using the validated fatty liver index, with a cutoff score of 60 or higher. Primary end points were the occurrence of major bleedings and cardiovascular events (CVEs). NAFLD was diagnosed in 732 of 1735 (42.2%) patients. Patients with NAFLD were younger, less frequently women, and more likely to be treated with NOACs and to have obesity, dyslipidemia, and persistent/permanent AF. During a median follow-up of 18.7 months (3155 patient-years), we recorded 78 major bleedings (incidence rate, 2.5% per year): 29 (2.1% per year) in patients with and 49 (2.7% per year) in patients without NAFLD (log-rank test P=.23). Univariate Cox proportional regression analysis showed no association of NAFLD with major bleedings (hazard ratio, 0.75; 95% CI, 0.47-1.20; P=.23). One hundred fifty-five CVEs occurred (incidence rate, 3.1% per year). No significant association was found between NAFLD and CVEs (log-rank test P=.12). In the entire population, NOAC use was associated with lower CVEs compared with VKAs (hazard ratio, 0.61; 95% CI, 0.42-0.89; P=.01). NAFLD is highly prevalent in AF but is not associated with higher bleeding or thrombotic risk.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>31753536</pmid><doi>10.1016/j.mayocp.2019.08.027</doi><tpages>8</tpages></addata></record>
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subjects Anticoagulants
Atherosclerosis
Atrial fibrillation
Body mass index
Cardiac arrhythmia
Cardiology
Diseases
Embolisms
Fatty liver
Fibrillation
Health risk assessment
Liver diseases
Medical research
Metabolism
Patients
Regression analysis
Risk factors
Stroke
Thromboembolism
Variables
Vitamins
title Prevalence and Impact of Nonalcoholic Fatty Liver Disease in Atrial Fibrillation
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