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 |
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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).
NAFLD is highly prevalent in AF but is not associated with higher bleeding or thrombotic risk.</description><identifier>ISSN: 0025-6196</identifier><identifier>EISSN: 1942-5546</identifier><identifier>DOI: 10.1016/j.mayocp.2019.08.027</identifier><identifier>PMID: 31753536</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>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</subject><ispartof>Mayo Clinic proceedings, 2020-03, Vol.95 (3), p.513-520</ispartof><rights>2019 Mayo Foundation for Medical Education and Research</rights><rights>Copyright © 2019 Mayo Foundation for Medical Education and Research. Published by Elsevier Inc. All rights reserved.</rights><rights>COPYRIGHT 2020 Frontline Medical Communications Inc.</rights><rights>Copyright Mayo Foundation for Medical Education and Research Mar 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-290e60bd5d653ef13beab2b7bbe9ddb4a2dcadec377600a9a5e9a537a1e388973</citedby><cites>FETCH-LOGICAL-c421t-290e60bd5d653ef13beab2b7bbe9ddb4a2dcadec377600a9a5e9a537a1e388973</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31753536$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pastori, Daniele</creatorcontrib><creatorcontrib>Sciacqua, Angela</creatorcontrib><creatorcontrib>Marcucci, Rossella</creatorcontrib><creatorcontrib>Farcomeni, Alessio</creatorcontrib><creatorcontrib>Perticone, Francesco</creatorcontrib><creatorcontrib>Del Ben, Maria</creatorcontrib><creatorcontrib>Angelico, Francesco</creatorcontrib><creatorcontrib>Baratta, Francesco</creatorcontrib><creatorcontrib>Pignatelli, Pasquale</creatorcontrib><creatorcontrib>Violi, Francesco</creatorcontrib><creatorcontrib>Saliola, Mirella</creatorcontrib><creatorcontrib>Santulli, Maria</creatorcontrib><creatorcontrib>Vasaturo, Fortunata</creatorcontrib><creatorcontrib>Casciaro, Marco Antonio</creatorcontrib><creatorcontrib>Cammisotto, Vittoria</creatorcontrib><creatorcontrib>Nocella, Cristina</creatorcontrib><creatorcontrib>Bartimoccia, Simona</creatorcontrib><creatorcontrib>Carnevale, Roberto</creatorcontrib><creatorcontrib>Iannilli, Claudia</creatorcontrib><creatorcontrib>Di Stefano, Tiziana</creatorcontrib><creatorcontrib>Iannucci, Patrizia</creatorcontrib><creatorcontrib>Sabbatini, Elio</creatorcontrib><creatorcontrib>the ATHERO-AF study group</creatorcontrib><creatorcontrib>ATHERO-AF study group</creatorcontrib><title>Prevalence and Impact of Nonalcoholic Fatty Liver Disease in Atrial Fibrillation</title><title>Mayo Clinic proceedings</title><addtitle>Mayo Clin Proc</addtitle><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.</description><subject>Anticoagulants</subject><subject>Atherosclerosis</subject><subject>Atrial fibrillation</subject><subject>Body mass index</subject><subject>Cardiac arrhythmia</subject><subject>Cardiology</subject><subject>Diseases</subject><subject>Embolisms</subject><subject>Fatty liver</subject><subject>Fibrillation</subject><subject>Health risk assessment</subject><subject>Liver diseases</subject><subject>Medical research</subject><subject>Metabolism</subject><subject>Patients</subject><subject>Regression analysis</subject><subject>Risk 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Impact of Nonalcoholic Fatty Liver Disease in Atrial Fibrillation</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-290e60bd5d653ef13beab2b7bbe9ddb4a2dcadec377600a9a5e9a537a1e388973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Anticoagulants</topic><topic>Atherosclerosis</topic><topic>Atrial fibrillation</topic><topic>Body mass index</topic><topic>Cardiac arrhythmia</topic><topic>Cardiology</topic><topic>Diseases</topic><topic>Embolisms</topic><topic>Fatty liver</topic><topic>Fibrillation</topic><topic>Health risk assessment</topic><topic>Liver diseases</topic><topic>Medical research</topic><topic>Metabolism</topic><topic>Patients</topic><topic>Regression analysis</topic><topic>Risk factors</topic><topic>Stroke</topic><topic>Thromboembolism</topic><topic>Variables</topic><topic>Vitamins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pastori, Daniele</creatorcontrib><creatorcontrib>Sciacqua, Angela</creatorcontrib><creatorcontrib>Marcucci, Rossella</creatorcontrib><creatorcontrib>Farcomeni, Alessio</creatorcontrib><creatorcontrib>Perticone, Francesco</creatorcontrib><creatorcontrib>Del Ben, Maria</creatorcontrib><creatorcontrib>Angelico, Francesco</creatorcontrib><creatorcontrib>Baratta, Francesco</creatorcontrib><creatorcontrib>Pignatelli, Pasquale</creatorcontrib><creatorcontrib>Violi, 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USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>Mayo Clinic proceedings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pastori, Daniele</au><au>Sciacqua, Angela</au><au>Marcucci, Rossella</au><au>Farcomeni, Alessio</au><au>Perticone, Francesco</au><au>Del Ben, Maria</au><au>Angelico, Francesco</au><au>Baratta, Francesco</au><au>Pignatelli, Pasquale</au><au>Violi, Francesco</au><au>Saliola, Mirella</au><au>Santulli, Maria</au><au>Vasaturo, Fortunata</au><au>Casciaro, Marco Antonio</au><au>Cammisotto, Vittoria</au><au>Nocella, Cristina</au><au>Bartimoccia, Simona</au><au>Carnevale, Roberto</au><au>Iannilli, Claudia</au><au>Di Stefano, Tiziana</au><au>Iannucci, Patrizia</au><au>Sabbatini, Elio</au><aucorp>the ATHERO-AF study group</aucorp><aucorp>ATHERO-AF study group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevalence and Impact of Nonalcoholic Fatty Liver Disease in Atrial Fibrillation</atitle><jtitle>Mayo Clinic proceedings</jtitle><addtitle>Mayo Clin Proc</addtitle><date>2020-03</date><risdate>2020</risdate><volume>95</volume><issue>3</issue><spage>513</spage><epage>520</epage><pages>513-520</pages><issn>0025-6196</issn><eissn>1942-5546</eissn><abstract>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.</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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