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Renin–angiotensin system inhibition and risk of infection and mortality in COVID‐19: a systematic review and meta‐analysis

Background Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2), the causative agent of COVID‐19, enters human cells by binding of its viral protein to the aminopeptidase angiotensin‐converting enzyme 2 (ACE2). This has led to speculation whether treatment with renin–angiotensin system (RAS)...

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Published in:Internal medicine journal 2020-12, Vol.50 (12), p.1468-1474
Main Authors: Koshy, Anoop N., Murphy, Alexandra C., Farouque, Omar, Ramchand, Jay, Burrell, Louise M., Yudi, Matias B.
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container_start_page 1468
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Murphy, Alexandra C.
Farouque, Omar
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Yudi, Matias B.
description Background Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2), the causative agent of COVID‐19, enters human cells by binding of its viral protein to the aminopeptidase angiotensin‐converting enzyme 2 (ACE2). This has led to speculation whether treatment with renin–angiotensin system (RAS) inhibitors was associated with an increased likelihood of a positive test for COVID‐19 and risk of mortality. Aims We performed a systematic review and meta‐analysis to investigate whether RAS inhibitors increased the likelihood of a positive test or death/severe illness in patients with COVID‐19. Methods A systematic search of MEDLINE, PubMed and EMBASE was conducted for studies stratified by the use of angiotensin‐converting enzyme inhibitors (ACEI) or angiotensin receptor blockers (ARB). Pooled analysis was performed using a random‐effects model. Results Seven trials of 73 122 patients were included. Overall, 16 624 (22.7%) patients had a positive COVID‐19 test and 7892 (10.8%) were on a RAS inhibitor. RAS inhibitors were not associated with higher likelihood of a positive COVID‐19 test result (odds ratio (OR) 0.97 (95% CI 0.97–1.05, P = 0.48) with low heterogeneity. This was comparable when stratifying by use of each medication class. The use of RAS inhibitors was also not associated with mortality or severe illness (OR 0.89, 95% CI 0.73–1.07, P = 0.21) with moderate heterogeneity. Conclusion Use of ACEI or ARB was not associated with a heightened susceptibility for a positive diagnosis of COVID‐19. Furthermore, they were not associated with increased illness severity or mortality due to COVID‐19. Randomised controlled trials are needed to address definitively the potential benefits or harms of RAS inhibitors in patients with COVID‐19.
doi_str_mv 10.1111/imj.15002
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This has led to speculation whether treatment with renin–angiotensin system (RAS) inhibitors was associated with an increased likelihood of a positive test for COVID‐19 and risk of mortality. Aims We performed a systematic review and meta‐analysis to investigate whether RAS inhibitors increased the likelihood of a positive test or death/severe illness in patients with COVID‐19. Methods A systematic search of MEDLINE, PubMed and EMBASE was conducted for studies stratified by the use of angiotensin‐converting enzyme inhibitors (ACEI) or angiotensin receptor blockers (ARB). Pooled analysis was performed using a random‐effects model. Results Seven trials of 73 122 patients were included. Overall, 16 624 (22.7%) patients had a positive COVID‐19 test and 7892 (10.8%) were on a RAS inhibitor. RAS inhibitors were not associated with higher likelihood of a positive COVID‐19 test result (odds ratio (OR) 0.97 (95% CI 0.97–1.05, P = 0.48) with low heterogeneity. This was comparable when stratifying by use of each medication class. The use of RAS inhibitors was also not associated with mortality or severe illness (OR 0.89, 95% CI 0.73–1.07, P = 0.21) with moderate heterogeneity. Conclusion Use of ACEI or ARB was not associated with a heightened susceptibility for a positive diagnosis of COVID‐19. Furthermore, they were not associated with increased illness severity or mortality due to COVID‐19. Randomised controlled trials are needed to address definitively the potential benefits or harms of RAS inhibitors in patients with COVID‐19.</description><identifier>ISSN: 1444-0903</identifier><identifier>EISSN: 1445-5994</identifier><identifier>DOI: 10.1111/imj.15002</identifier><identifier>PMID: 33191600</identifier><language>eng</language><publisher>Melbourne: John Wiley &amp; Sons Australia, Ltd</publisher><subject>ace inhibitor ; ACE2 ; Aminopeptidase ; Angiotensin ; Angiotensin Receptor Antagonists - administration &amp; dosage ; Angiotensin Receptor Antagonists - adverse effects ; Angiotensin-converting enzyme 2 ; Angiotensin-Converting Enzyme 2 - antagonists &amp; inhibitors ; Angiotensin-Converting Enzyme 2 - metabolism ; Angiotensin-Converting Enzyme Inhibitors - administration &amp; dosage ; Angiotensin-Converting Enzyme Inhibitors - adverse effects ; Case-Control Studies ; Clinical trials ; Coronaviruses ; COVID-19 ; COVID-19 - diagnosis ; COVID-19 - metabolism ; COVID-19 - mortality ; Enzymes ; Humans ; Meta-analysis ; metaanalysis ; Mortality ; Mortality - trends ; Original ; Renin ; renin angiotensin inhibitor ; Renin-Angiotensin System - drug effects ; Renin-Angiotensin System - physiology ; Retrospective Studies ; Risk Factors ; Severe acute respiratory syndrome coronavirus 2 ; Systematic review</subject><ispartof>Internal medicine journal, 2020-12, Vol.50 (12), p.1468-1474</ispartof><rights>2020 Royal Australasian College of Physicians</rights><rights>2020 Royal Australasian College of Physicians.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5092-e8f2fbf5a77976f615f694c5bec8004dc041a8980a3f17c9dad994dda661b0353</citedby><cites>FETCH-LOGICAL-c5092-e8f2fbf5a77976f615f694c5bec8004dc041a8980a3f17c9dad994dda661b0353</cites><orcidid>0000-0002-8741-8631 ; 0000-0002-4248-7537</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33191600$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Koshy, Anoop N.</creatorcontrib><creatorcontrib>Murphy, Alexandra C.</creatorcontrib><creatorcontrib>Farouque, Omar</creatorcontrib><creatorcontrib>Ramchand, Jay</creatorcontrib><creatorcontrib>Burrell, Louise M.</creatorcontrib><creatorcontrib>Yudi, Matias B.</creatorcontrib><title>Renin–angiotensin system inhibition and risk of infection and mortality in COVID‐19: a systematic review and meta‐analysis</title><title>Internal medicine journal</title><addtitle>Intern Med J</addtitle><description>Background Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2), the causative agent of COVID‐19, enters human cells by binding of its viral protein to the aminopeptidase angiotensin‐converting enzyme 2 (ACE2). This has led to speculation whether treatment with renin–angiotensin system (RAS) inhibitors was associated with an increased likelihood of a positive test for COVID‐19 and risk of mortality. Aims We performed a systematic review and meta‐analysis to investigate whether RAS inhibitors increased the likelihood of a positive test or death/severe illness in patients with COVID‐19. Methods A systematic search of MEDLINE, PubMed and EMBASE was conducted for studies stratified by the use of angiotensin‐converting enzyme inhibitors (ACEI) or angiotensin receptor blockers (ARB). Pooled analysis was performed using a random‐effects model. Results Seven trials of 73 122 patients were included. Overall, 16 624 (22.7%) patients had a positive COVID‐19 test and 7892 (10.8%) were on a RAS inhibitor. RAS inhibitors were not associated with higher likelihood of a positive COVID‐19 test result (odds ratio (OR) 0.97 (95% CI 0.97–1.05, P = 0.48) with low heterogeneity. This was comparable when stratifying by use of each medication class. The use of RAS inhibitors was also not associated with mortality or severe illness (OR 0.89, 95% CI 0.73–1.07, P = 0.21) with moderate heterogeneity. Conclusion Use of ACEI or ARB was not associated with a heightened susceptibility for a positive diagnosis of COVID‐19. Furthermore, they were not associated with increased illness severity or mortality due to COVID‐19. 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dosage</topic><topic>Angiotensin Receptor Antagonists - adverse effects</topic><topic>Angiotensin-converting enzyme 2</topic><topic>Angiotensin-Converting Enzyme 2 - antagonists &amp; inhibitors</topic><topic>Angiotensin-Converting Enzyme 2 - metabolism</topic><topic>Angiotensin-Converting Enzyme Inhibitors - administration &amp; dosage</topic><topic>Angiotensin-Converting Enzyme Inhibitors - adverse effects</topic><topic>Case-Control Studies</topic><topic>Clinical trials</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>COVID-19 - diagnosis</topic><topic>COVID-19 - metabolism</topic><topic>COVID-19 - mortality</topic><topic>Enzymes</topic><topic>Humans</topic><topic>Meta-analysis</topic><topic>metaanalysis</topic><topic>Mortality</topic><topic>Mortality - trends</topic><topic>Original</topic><topic>Renin</topic><topic>renin angiotensin inhibitor</topic><topic>Renin-Angiotensin System - drug effects</topic><topic>Renin-Angiotensin System - physiology</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koshy, Anoop N.</creatorcontrib><creatorcontrib>Murphy, Alexandra C.</creatorcontrib><creatorcontrib>Farouque, Omar</creatorcontrib><creatorcontrib>Ramchand, Jay</creatorcontrib><creatorcontrib>Burrell, Louise M.</creatorcontrib><creatorcontrib>Yudi, Matias B.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Internal medicine journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koshy, Anoop N.</au><au>Murphy, Alexandra C.</au><au>Farouque, Omar</au><au>Ramchand, Jay</au><au>Burrell, Louise M.</au><au>Yudi, Matias B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Renin–angiotensin system inhibition and risk of infection and mortality in COVID‐19: a systematic review and meta‐analysis</atitle><jtitle>Internal medicine journal</jtitle><addtitle>Intern Med J</addtitle><date>2020-12</date><risdate>2020</risdate><volume>50</volume><issue>12</issue><spage>1468</spage><epage>1474</epage><pages>1468-1474</pages><issn>1444-0903</issn><eissn>1445-5994</eissn><abstract>Background Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2), the causative agent of COVID‐19, enters human cells by binding of its viral protein to the aminopeptidase angiotensin‐converting enzyme 2 (ACE2). This has led to speculation whether treatment with renin–angiotensin system (RAS) inhibitors was associated with an increased likelihood of a positive test for COVID‐19 and risk of mortality. Aims We performed a systematic review and meta‐analysis to investigate whether RAS inhibitors increased the likelihood of a positive test or death/severe illness in patients with COVID‐19. Methods A systematic search of MEDLINE, PubMed and EMBASE was conducted for studies stratified by the use of angiotensin‐converting enzyme inhibitors (ACEI) or angiotensin receptor blockers (ARB). Pooled analysis was performed using a random‐effects model. Results Seven trials of 73 122 patients were included. Overall, 16 624 (22.7%) patients had a positive COVID‐19 test and 7892 (10.8%) were on a RAS inhibitor. RAS inhibitors were not associated with higher likelihood of a positive COVID‐19 test result (odds ratio (OR) 0.97 (95% CI 0.97–1.05, P = 0.48) with low heterogeneity. This was comparable when stratifying by use of each medication class. The use of RAS inhibitors was also not associated with mortality or severe illness (OR 0.89, 95% CI 0.73–1.07, P = 0.21) with moderate heterogeneity. Conclusion Use of ACEI or ARB was not associated with a heightened susceptibility for a positive diagnosis of COVID‐19. Furthermore, they were not associated with increased illness severity or mortality due to COVID‐19. Randomised controlled trials are needed to address definitively the potential benefits or harms of RAS inhibitors in patients with COVID‐19.</abstract><cop>Melbourne</cop><pub>John Wiley &amp; Sons Australia, Ltd</pub><pmid>33191600</pmid><doi>10.1111/imj.15002</doi><tpages>150</tpages><orcidid>https://orcid.org/0000-0002-8741-8631</orcidid><orcidid>https://orcid.org/0000-0002-4248-7537</orcidid><oa>free_for_read</oa></addata></record>
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subjects ace inhibitor
ACE2
Aminopeptidase
Angiotensin
Angiotensin Receptor Antagonists - administration & dosage
Angiotensin Receptor Antagonists - adverse effects
Angiotensin-converting enzyme 2
Angiotensin-Converting Enzyme 2 - antagonists & inhibitors
Angiotensin-Converting Enzyme 2 - metabolism
Angiotensin-Converting Enzyme Inhibitors - administration & dosage
Angiotensin-Converting Enzyme Inhibitors - adverse effects
Case-Control Studies
Clinical trials
Coronaviruses
COVID-19
COVID-19 - diagnosis
COVID-19 - metabolism
COVID-19 - mortality
Enzymes
Humans
Meta-analysis
metaanalysis
Mortality
Mortality - trends
Original
Renin
renin angiotensin inhibitor
Renin-Angiotensin System - drug effects
Renin-Angiotensin System - physiology
Retrospective Studies
Risk Factors
Severe acute respiratory syndrome coronavirus 2
Systematic review
title Renin–angiotensin system inhibition and risk of infection and mortality in COVID‐19: a systematic review and meta‐analysis
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