Prevention of atrial fibrillation by Renin-Angiotensin system inhibition a meta-analysis
The authors reviewed published clinical trial data on the effects of renin-angiotensin system (RAS) inhibition for the prevention of atrial fibrillation (AF), aiming to define when RAS inhibition is most effective. Individual studies examining the effects of RAS inhibition on AF prevention have repo...
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Veröffentlicht in: | Journal of the American College of Cardiology 2010-05, Vol.55 (21), p.2299-2307 |
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creator | Schneider, Markus P Hua, Tsushung A Böhm, Michael Wachtell, Kristian Kjeldsen, Sverre E Schmieder, Roland E |
description | The authors reviewed published clinical trial data on the effects of renin-angiotensin system (RAS) inhibition for the prevention of atrial fibrillation (AF), aiming to define when RAS inhibition is most effective.
Individual studies examining the effects of RAS inhibition on AF prevention have reported controversial results.
All published randomized controlled trials reporting the effects of treatment with angiotensin-converting enzyme inhibitors or angiotensin receptor blockers in the primary or secondary prevention of AF were included.
A total of 23 randomized controlled trials with 87,048 patients were analyzed. In primary prevention, 6 trials in hypertension, 2 trials in myocardial infarction, and 3 trials in heart failure were included (some being post-hoc analyses of randomized controlled trials). In secondary prevention, 8 trials after cardioversion and 4 trials assessing the medical prevention of recurrence were included. Overall, RAS inhibition reduced the odds ratio for AF by 33% (p < 0.00001), but there was substantial heterogeneity among trials. In primary prevention, RAS inhibition was effective in patients with heart failure and those with hypertension and left ventricular hypertrophy but not in post-myocardial infarction patients overall. In secondary prevention, RAS inhibition was often administered in addition to antiarrhythmic drugs, including amiodarone, further reducing the odds for AF recurrence after cardioversion by 45% (p = 0.01) and in patients on medical therapy by 63% (p < 0.00001).
This analysis supports the concept of RAS inhibition as an emerging treatment for the primary and secondary prevention of AF but acknowledges the fact that some of the primary prevention trials were post-hoc analyses. Further areas of uncertainty include potential differences among specific RAS inhibitors and possible interactions or synergistic effects with antiarrhythmic drugs. |
doi_str_mv | 10.1016/j.jacc.2010.01.043 |
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Individual studies examining the effects of RAS inhibition on AF prevention have reported controversial results.
All published randomized controlled trials reporting the effects of treatment with angiotensin-converting enzyme inhibitors or angiotensin receptor blockers in the primary or secondary prevention of AF were included.
A total of 23 randomized controlled trials with 87,048 patients were analyzed. In primary prevention, 6 trials in hypertension, 2 trials in myocardial infarction, and 3 trials in heart failure were included (some being post-hoc analyses of randomized controlled trials). In secondary prevention, 8 trials after cardioversion and 4 trials assessing the medical prevention of recurrence were included. Overall, RAS inhibition reduced the odds ratio for AF by 33% (p < 0.00001), but there was substantial heterogeneity among trials. In primary prevention, RAS inhibition was effective in patients with heart failure and those with hypertension and left ventricular hypertrophy but not in post-myocardial infarction patients overall. In secondary prevention, RAS inhibition was often administered in addition to antiarrhythmic drugs, including amiodarone, further reducing the odds for AF recurrence after cardioversion by 45% (p = 0.01) and in patients on medical therapy by 63% (p < 0.00001).
This analysis supports the concept of RAS inhibition as an emerging treatment for the primary and secondary prevention of AF but acknowledges the fact that some of the primary prevention trials were post-hoc analyses. Further areas of uncertainty include potential differences among specific RAS inhibitors and possible interactions or synergistic effects with antiarrhythmic drugs.</description><identifier>ISSN: 0735-1097</identifier><identifier>EISSN: 1558-3597</identifier><identifier>DOI: 10.1016/j.jacc.2010.01.043</identifier><identifier>PMID: 20488299</identifier><language>eng</language><publisher>United States: Elsevier Limited</publisher><subject>Angiotensin-Converting Enzyme Inhibitors - therapeutic use ; Animals ; Anti-Arrhythmia Agents - therapeutic use ; Atrial Fibrillation - diagnosis ; Atrial Fibrillation - drug therapy ; Atrial Fibrillation - mortality ; Atrial Fibrillation - prevention & control ; Cardiac arrhythmia ; Cardiology ; Confidence intervals ; Disease prevention ; Drug therapy ; Electrocardiography ; Enzymes ; Female ; Heart attacks ; Heart failure ; Humans ; Hypertension ; Male ; Mortality ; Potassium ; Primary Prevention - methods ; Prognosis ; Randomized Controlled Trials as Topic ; Renin-Angiotensin System - drug effects ; Risk Assessment ; Severity of Illness Index ; Studies ; Survival Analysis ; Treatment Outcome</subject><ispartof>Journal of the American College of Cardiology, 2010-05, Vol.55 (21), p.2299-2307</ispartof><rights>Copyright (c) 2010 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited May 25, 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20488299$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schneider, Markus P</creatorcontrib><creatorcontrib>Hua, Tsushung A</creatorcontrib><creatorcontrib>Böhm, Michael</creatorcontrib><creatorcontrib>Wachtell, Kristian</creatorcontrib><creatorcontrib>Kjeldsen, Sverre E</creatorcontrib><creatorcontrib>Schmieder, Roland E</creatorcontrib><title>Prevention of atrial fibrillation by Renin-Angiotensin system inhibition a meta-analysis</title><title>Journal of the American College of Cardiology</title><addtitle>J Am Coll Cardiol</addtitle><description>The authors reviewed published clinical trial data on the effects of renin-angiotensin system (RAS) inhibition for the prevention of atrial fibrillation (AF), aiming to define when RAS inhibition is most effective.
Individual studies examining the effects of RAS inhibition on AF prevention have reported controversial results.
All published randomized controlled trials reporting the effects of treatment with angiotensin-converting enzyme inhibitors or angiotensin receptor blockers in the primary or secondary prevention of AF were included.
A total of 23 randomized controlled trials with 87,048 patients were analyzed. In primary prevention, 6 trials in hypertension, 2 trials in myocardial infarction, and 3 trials in heart failure were included (some being post-hoc analyses of randomized controlled trials). In secondary prevention, 8 trials after cardioversion and 4 trials assessing the medical prevention of recurrence were included. Overall, RAS inhibition reduced the odds ratio for AF by 33% (p < 0.00001), but there was substantial heterogeneity among trials. In primary prevention, RAS inhibition was effective in patients with heart failure and those with hypertension and left ventricular hypertrophy but not in post-myocardial infarction patients overall. In secondary prevention, RAS inhibition was often administered in addition to antiarrhythmic drugs, including amiodarone, further reducing the odds for AF recurrence after cardioversion by 45% (p = 0.01) and in patients on medical therapy by 63% (p < 0.00001).
This analysis supports the concept of RAS inhibition as an emerging treatment for the primary and secondary prevention of AF but acknowledges the fact that some of the primary prevention trials were post-hoc analyses. Further areas of uncertainty include potential differences among specific RAS inhibitors and possible interactions or synergistic effects with antiarrhythmic drugs.</description><subject>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</subject><subject>Animals</subject><subject>Anti-Arrhythmia Agents - therapeutic use</subject><subject>Atrial Fibrillation - diagnosis</subject><subject>Atrial Fibrillation - drug therapy</subject><subject>Atrial Fibrillation - mortality</subject><subject>Atrial Fibrillation - prevention & control</subject><subject>Cardiac arrhythmia</subject><subject>Cardiology</subject><subject>Confidence intervals</subject><subject>Disease prevention</subject><subject>Drug therapy</subject><subject>Electrocardiography</subject><subject>Enzymes</subject><subject>Female</subject><subject>Heart attacks</subject><subject>Heart failure</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Male</subject><subject>Mortality</subject><subject>Potassium</subject><subject>Primary Prevention - methods</subject><subject>Prognosis</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Renin-Angiotensin System - drug effects</subject><subject>Risk Assessment</subject><subject>Severity of Illness Index</subject><subject>Studies</subject><subject>Survival Analysis</subject><subject>Treatment Outcome</subject><issn>0735-1097</issn><issn>1558-3597</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkE9LxDAQxYMo7rr6BTxIwIOn1knSNMlxEf_BgiIK3krapprSpmuTCv32hnW9OHOY4fHj8WYQOieQEiD5dZu2uqpSClEAkkLGDtCScC4TxpU4REsQjCcElFigE-9bAMglUcdoQSGTkiq1RO_Po_k2LtjB4aHBOoxWd7ix5Wi7Tu_kcsYvxlmXrN2HHYJx3jrsZx9Mj637tKXdYRr3JuhEO93N3vpTdNTozpuz_Vyht7vb15uHZPN0_3iz3iRbymRIJJGK1TkniuZCKNC05BnnVaWAaM1ilYzReGZcqOFMQ02Zaeqs5srQSrAVuvr13Y7D12R8KHrrKxPDOzNMvhDRIssEgUhe_iPbYRpjXF8QDjnNZexIXeypqexNXWxH2-txLv5exn4Ab2FuaQ</recordid><startdate>20100525</startdate><enddate>20100525</enddate><creator>Schneider, Markus P</creator><creator>Hua, Tsushung A</creator><creator>Böhm, Michael</creator><creator>Wachtell, Kristian</creator><creator>Kjeldsen, Sverre E</creator><creator>Schmieder, Roland E</creator><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7T5</scope><scope>7TK</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20100525</creationdate><title>Prevention of atrial fibrillation by Renin-Angiotensin system inhibition a meta-analysis</title><author>Schneider, Markus P ; Hua, Tsushung A ; Böhm, Michael ; Wachtell, Kristian ; Kjeldsen, Sverre E ; Schmieder, Roland E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p238t-81893d6519267790a2b5455cc901aa3333b332acc33b2e53a0d23efd4d59e2c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</topic><topic>Animals</topic><topic>Anti-Arrhythmia Agents - therapeutic use</topic><topic>Atrial Fibrillation - diagnosis</topic><topic>Atrial Fibrillation - drug therapy</topic><topic>Atrial Fibrillation - mortality</topic><topic>Atrial Fibrillation - prevention & control</topic><topic>Cardiac arrhythmia</topic><topic>Cardiology</topic><topic>Confidence intervals</topic><topic>Disease prevention</topic><topic>Drug therapy</topic><topic>Electrocardiography</topic><topic>Enzymes</topic><topic>Female</topic><topic>Heart attacks</topic><topic>Heart failure</topic><topic>Humans</topic><topic>Hypertension</topic><topic>Male</topic><topic>Mortality</topic><topic>Potassium</topic><topic>Primary Prevention - methods</topic><topic>Prognosis</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Renin-Angiotensin System - drug effects</topic><topic>Risk Assessment</topic><topic>Severity of Illness Index</topic><topic>Studies</topic><topic>Survival Analysis</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schneider, Markus P</creatorcontrib><creatorcontrib>Hua, Tsushung A</creatorcontrib><creatorcontrib>Böhm, Michael</creatorcontrib><creatorcontrib>Wachtell, Kristian</creatorcontrib><creatorcontrib>Kjeldsen, Sverre E</creatorcontrib><creatorcontrib>Schmieder, Roland E</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American College of Cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schneider, Markus P</au><au>Hua, Tsushung A</au><au>Böhm, Michael</au><au>Wachtell, Kristian</au><au>Kjeldsen, Sverre E</au><au>Schmieder, Roland E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevention of atrial fibrillation by Renin-Angiotensin system inhibition a meta-analysis</atitle><jtitle>Journal of the American College of Cardiology</jtitle><addtitle>J Am Coll Cardiol</addtitle><date>2010-05-25</date><risdate>2010</risdate><volume>55</volume><issue>21</issue><spage>2299</spage><epage>2307</epage><pages>2299-2307</pages><issn>0735-1097</issn><eissn>1558-3597</eissn><abstract>The authors reviewed published clinical trial data on the effects of renin-angiotensin system (RAS) inhibition for the prevention of atrial fibrillation (AF), aiming to define when RAS inhibition is most effective.
Individual studies examining the effects of RAS inhibition on AF prevention have reported controversial results.
All published randomized controlled trials reporting the effects of treatment with angiotensin-converting enzyme inhibitors or angiotensin receptor blockers in the primary or secondary prevention of AF were included.
A total of 23 randomized controlled trials with 87,048 patients were analyzed. In primary prevention, 6 trials in hypertension, 2 trials in myocardial infarction, and 3 trials in heart failure were included (some being post-hoc analyses of randomized controlled trials). In secondary prevention, 8 trials after cardioversion and 4 trials assessing the medical prevention of recurrence were included. Overall, RAS inhibition reduced the odds ratio for AF by 33% (p < 0.00001), but there was substantial heterogeneity among trials. In primary prevention, RAS inhibition was effective in patients with heart failure and those with hypertension and left ventricular hypertrophy but not in post-myocardial infarction patients overall. In secondary prevention, RAS inhibition was often administered in addition to antiarrhythmic drugs, including amiodarone, further reducing the odds for AF recurrence after cardioversion by 45% (p = 0.01) and in patients on medical therapy by 63% (p < 0.00001).
This analysis supports the concept of RAS inhibition as an emerging treatment for the primary and secondary prevention of AF but acknowledges the fact that some of the primary prevention trials were post-hoc analyses. Further areas of uncertainty include potential differences among specific RAS inhibitors and possible interactions or synergistic effects with antiarrhythmic drugs.</abstract><cop>United States</cop><pub>Elsevier Limited</pub><pmid>20488299</pmid><doi>10.1016/j.jacc.2010.01.043</doi><tpages>9</tpages></addata></record> |
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subjects | Angiotensin-Converting Enzyme Inhibitors - therapeutic use Animals Anti-Arrhythmia Agents - therapeutic use Atrial Fibrillation - diagnosis Atrial Fibrillation - drug therapy Atrial Fibrillation - mortality Atrial Fibrillation - prevention & control Cardiac arrhythmia Cardiology Confidence intervals Disease prevention Drug therapy Electrocardiography Enzymes Female Heart attacks Heart failure Humans Hypertension Male Mortality Potassium Primary Prevention - methods Prognosis Randomized Controlled Trials as Topic Renin-Angiotensin System - drug effects Risk Assessment Severity of Illness Index Studies Survival Analysis Treatment Outcome |
title | Prevention of atrial fibrillation by Renin-Angiotensin system inhibition a meta-analysis |
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