Circulating plasma concentrations of angiotensin-converting enzyme 2 in men and women with heart failure and effects of renin–angiotensin–aldosterone inhibitors
Abstract Aims The current pandemic coronavirus SARS-CoV-2 infects a wide age group but predominantly elderly individuals, especially men and those with cardiovascular disease. Recent reports suggest an association with use of renin–angiotensin–aldosterone system (RAAS) inhibitors. Angiotensin-conver...
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Veröffentlicht in: | European heart journal 2020-05, Vol.41 (19), p.1810-1817 |
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creator | Sama, Iziah E Ravera, Alice Santema, Bernadet T van Goor, Harry ter Maaten, Jozine M Cleland, John G F Rienstra, Michiel Friedrich, Alex W Samani, Nilesh J Ng, Leong L Dickstein, Kenneth Lang, Chim C Filippatos, Gerasimos Anker, Stefan D Ponikowski, Piotr Metra, Marco van Veldhuisen, Dirk J Voors, Adriaan A |
description | Abstract
Aims
The current pandemic coronavirus SARS-CoV-2 infects a wide age group but predominantly elderly individuals, especially men and those with cardiovascular disease. Recent reports suggest an association with use of renin–angiotensin–aldosterone system (RAAS) inhibitors. Angiotensin-converting enzyme 2 (ACE2) is a functional receptor for coronaviruses. Higher ACE2 concentrations might lead to increased vulnerability to SARS-CoV-2 in patients on RAAS inhibitors.
Methods and results
We measured ACE2 concentrations in 1485 men and 537 women with heart failure (index cohort). Results were validated in 1123 men and 575 women (validation cohort).
The median age was 69 years for men and 75 years for women. The strongest predictor of elevated concentrations of ACE2 in both cohorts was male sex (estimate = 0.26, P < 0.001; and 0.19, P < 0.001, respectively). In the index cohort, use of ACE inhibitors, angiotensin receptor blockers (ARBs), or mineralocorticoid receptor antagonists (MRAs) was not an independent predictor of plasma ACE2. In the validation cohort, ACE inhibitor (estimate = –0.17, P = 0.002) and ARB use (estimate = –0.15, P = 0.03) were independent predictors of lower plasma ACE2, while use of an MRA (estimate = 0.11, P = 0.04) was an independent predictor of higher plasma ACE2 concentrations.
Conclusion
In two independent cohorts of patients with heart failure, plasma concentrations of ACE2 were higher in men than in women, but use of neither an ACE inhibitor nor an ARB was associated with higher plasma ACE2 concentrations. These data might explain the higher incidence and fatality rate of COVID-19 in men, but do not support previous reports suggesting that ACE inhibitors or ARBs increase the vulnerability for COVID-19 through increased plasma ACE2 concentrations. |
doi_str_mv | 10.1093/eurheartj/ehaa373 |
format | Article |
fullrecord | <record><control><sourceid>oup_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7239195</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1093/eurheartj/ehaa373</oup_id><sourcerecordid>10.1093/eurheartj/ehaa373</sourcerecordid><originalsourceid>FETCH-LOGICAL-c394t-a9b46f88faa31802630856b505f09395611a286a98dee5d91516fdc8d2fb97fc3</originalsourceid><addsrcrecordid>eNqNkc1OGzEUha0KVMLPA3SD_ABMscexY2-QUAQtElI3ILEbeWauM0YzdmR7QGHFO_AKfbI-SZ2ERnTHyj_33O_a5yD0jZLvlCh2DmPoQIf0eA6d1mzGvqAJ5WVZKDHle2hCqOKFEPLhAB3G-EgIkYKKr-iAlUxKLvgE_Z7b0Iy9TtYt8LLXcdC48a4Bl0K-9C5ib7B2C-sTuGhdkatPEDZ6cC-rAXCJrcMDuCxr8bNf755t6vDmbdho248BNkUwBpq0QQZw1v15ffuAXp_61scEwTvI0M7WNvkQj9G-0X2Ek_f1CN1fX93Nfxa3v37czC9vi4apaSq0qqfCSGmyF1SSUjCSP1lzwk12S3FBqS6l0Eq2ALxVlFNh2ka2panVzDTsCF1sucuxHqDdmtBXy2AHHVaV17b6v-JsVy38UzUrmcpeZwDdAprgYwxgdr2UVOvIql1k1Xtkuef049Bdx7-MsuBsK_Dj8hO8v-4Xro8</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Circulating plasma concentrations of angiotensin-converting enzyme 2 in men and women with heart failure and effects of renin–angiotensin–aldosterone inhibitors</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Sama, Iziah E ; Ravera, Alice ; Santema, Bernadet T ; van Goor, Harry ; ter Maaten, Jozine M ; Cleland, John G F ; Rienstra, Michiel ; Friedrich, Alex W ; Samani, Nilesh J ; Ng, Leong L ; Dickstein, Kenneth ; Lang, Chim C ; Filippatos, Gerasimos ; Anker, Stefan D ; Ponikowski, Piotr ; Metra, Marco ; van Veldhuisen, Dirk J ; Voors, Adriaan A</creator><creatorcontrib>Sama, Iziah E ; Ravera, Alice ; Santema, Bernadet T ; van Goor, Harry ; ter Maaten, Jozine M ; Cleland, John G F ; Rienstra, Michiel ; Friedrich, Alex W ; Samani, Nilesh J ; Ng, Leong L ; Dickstein, Kenneth ; Lang, Chim C ; Filippatos, Gerasimos ; Anker, Stefan D ; Ponikowski, Piotr ; Metra, Marco ; van Veldhuisen, Dirk J ; Voors, Adriaan A</creatorcontrib><description>Abstract
Aims
The current pandemic coronavirus SARS-CoV-2 infects a wide age group but predominantly elderly individuals, especially men and those with cardiovascular disease. Recent reports suggest an association with use of renin–angiotensin–aldosterone system (RAAS) inhibitors. Angiotensin-converting enzyme 2 (ACE2) is a functional receptor for coronaviruses. Higher ACE2 concentrations might lead to increased vulnerability to SARS-CoV-2 in patients on RAAS inhibitors.
Methods and results
We measured ACE2 concentrations in 1485 men and 537 women with heart failure (index cohort). Results were validated in 1123 men and 575 women (validation cohort).
The median age was 69 years for men and 75 years for women. The strongest predictor of elevated concentrations of ACE2 in both cohorts was male sex (estimate = 0.26, P < 0.001; and 0.19, P < 0.001, respectively). In the index cohort, use of ACE inhibitors, angiotensin receptor blockers (ARBs), or mineralocorticoid receptor antagonists (MRAs) was not an independent predictor of plasma ACE2. In the validation cohort, ACE inhibitor (estimate = –0.17, P = 0.002) and ARB use (estimate = –0.15, P = 0.03) were independent predictors of lower plasma ACE2, while use of an MRA (estimate = 0.11, P = 0.04) was an independent predictor of higher plasma ACE2 concentrations.
Conclusion
In two independent cohorts of patients with heart failure, plasma concentrations of ACE2 were higher in men than in women, but use of neither an ACE inhibitor nor an ARB was associated with higher plasma ACE2 concentrations. These data might explain the higher incidence and fatality rate of COVID-19 in men, but do not support previous reports suggesting that ACE inhibitors or ARBs increase the vulnerability for COVID-19 through increased plasma ACE2 concentrations.</description><identifier>ISSN: 0195-668X</identifier><identifier>EISSN: 1522-9645</identifier><identifier>DOI: 10.1093/eurheartj/ehaa373</identifier><identifier>PMID: 32388565</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Aged ; Angiotensin Receptor Antagonists - therapeutic use ; Angiotensin-Converting Enzyme 2 ; Angiotensin-Converting Enzyme Inhibitors - therapeutic use ; Betacoronavirus ; Coronavirus Infections ; COVID-19 ; Editor's Choice ; Europe ; Fast Track Clinical Research ; Female ; Heart Failure - blood ; Humans ; Male ; Middle Aged ; Mineralocorticoid Receptor Antagonists - therapeutic use ; Pandemics ; Peptidyl-Dipeptidase A - blood ; Pneumonia, Viral ; Renin-Angiotensin System - drug effects ; SARS-CoV-2 ; Sex Factors</subject><ispartof>European heart journal, 2020-05, Vol.41 (19), p.1810-1817</ispartof><rights>The Author(s) 2020. Published by Oxford University Press on behalf of the European Society of Cardiology. 2020</rights><rights>Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2020. For permissions, please email: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c394t-a9b46f88faa31802630856b505f09395611a286a98dee5d91516fdc8d2fb97fc3</citedby><cites>FETCH-LOGICAL-c394t-a9b46f88faa31802630856b505f09395611a286a98dee5d91516fdc8d2fb97fc3</cites><orcidid>0000-0002-2581-070X ; 0000-0002-6553-5749 ; 0000-0002-4663-7213 ; 0000-0003-3331-7314 ; 0000-0002-5417-4415</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32388565$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sama, Iziah E</creatorcontrib><creatorcontrib>Ravera, Alice</creatorcontrib><creatorcontrib>Santema, Bernadet T</creatorcontrib><creatorcontrib>van Goor, Harry</creatorcontrib><creatorcontrib>ter Maaten, Jozine M</creatorcontrib><creatorcontrib>Cleland, John G F</creatorcontrib><creatorcontrib>Rienstra, Michiel</creatorcontrib><creatorcontrib>Friedrich, Alex W</creatorcontrib><creatorcontrib>Samani, Nilesh J</creatorcontrib><creatorcontrib>Ng, Leong L</creatorcontrib><creatorcontrib>Dickstein, Kenneth</creatorcontrib><creatorcontrib>Lang, Chim C</creatorcontrib><creatorcontrib>Filippatos, Gerasimos</creatorcontrib><creatorcontrib>Anker, Stefan D</creatorcontrib><creatorcontrib>Ponikowski, Piotr</creatorcontrib><creatorcontrib>Metra, Marco</creatorcontrib><creatorcontrib>van Veldhuisen, Dirk J</creatorcontrib><creatorcontrib>Voors, Adriaan A</creatorcontrib><title>Circulating plasma concentrations of angiotensin-converting enzyme 2 in men and women with heart failure and effects of renin–angiotensin–aldosterone inhibitors</title><title>European heart journal</title><addtitle>Eur Heart J</addtitle><description>Abstract
Aims
The current pandemic coronavirus SARS-CoV-2 infects a wide age group but predominantly elderly individuals, especially men and those with cardiovascular disease. Recent reports suggest an association with use of renin–angiotensin–aldosterone system (RAAS) inhibitors. Angiotensin-converting enzyme 2 (ACE2) is a functional receptor for coronaviruses. Higher ACE2 concentrations might lead to increased vulnerability to SARS-CoV-2 in patients on RAAS inhibitors.
Methods and results
We measured ACE2 concentrations in 1485 men and 537 women with heart failure (index cohort). Results were validated in 1123 men and 575 women (validation cohort).
The median age was 69 years for men and 75 years for women. The strongest predictor of elevated concentrations of ACE2 in both cohorts was male sex (estimate = 0.26, P < 0.001; and 0.19, P < 0.001, respectively). In the index cohort, use of ACE inhibitors, angiotensin receptor blockers (ARBs), or mineralocorticoid receptor antagonists (MRAs) was not an independent predictor of plasma ACE2. In the validation cohort, ACE inhibitor (estimate = –0.17, P = 0.002) and ARB use (estimate = –0.15, P = 0.03) were independent predictors of lower plasma ACE2, while use of an MRA (estimate = 0.11, P = 0.04) was an independent predictor of higher plasma ACE2 concentrations.
Conclusion
In two independent cohorts of patients with heart failure, plasma concentrations of ACE2 were higher in men than in women, but use of neither an ACE inhibitor nor an ARB was associated with higher plasma ACE2 concentrations. These data might explain the higher incidence and fatality rate of COVID-19 in men, but do not support previous reports suggesting that ACE inhibitors or ARBs increase the vulnerability for COVID-19 through increased plasma ACE2 concentrations.</description><subject>Aged</subject><subject>Angiotensin Receptor Antagonists - therapeutic use</subject><subject>Angiotensin-Converting Enzyme 2</subject><subject>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</subject><subject>Betacoronavirus</subject><subject>Coronavirus Infections</subject><subject>COVID-19</subject><subject>Editor's Choice</subject><subject>Europe</subject><subject>Fast Track Clinical Research</subject><subject>Female</subject><subject>Heart Failure - blood</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mineralocorticoid Receptor Antagonists - therapeutic use</subject><subject>Pandemics</subject><subject>Peptidyl-Dipeptidase A - blood</subject><subject>Pneumonia, Viral</subject><subject>Renin-Angiotensin System - drug effects</subject><subject>SARS-CoV-2</subject><subject>Sex Factors</subject><issn>0195-668X</issn><issn>1522-9645</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><sourceid>EIF</sourceid><recordid>eNqNkc1OGzEUha0KVMLPA3SD_ABMscexY2-QUAQtElI3ILEbeWauM0YzdmR7QGHFO_AKfbI-SZ2ERnTHyj_33O_a5yD0jZLvlCh2DmPoQIf0eA6d1mzGvqAJ5WVZKDHle2hCqOKFEPLhAB3G-EgIkYKKr-iAlUxKLvgE_Z7b0Iy9TtYt8LLXcdC48a4Bl0K-9C5ib7B2C-sTuGhdkatPEDZ6cC-rAXCJrcMDuCxr8bNf755t6vDmbdho248BNkUwBpq0QQZw1v15ffuAXp_61scEwTvI0M7WNvkQj9G-0X2Ek_f1CN1fX93Nfxa3v37czC9vi4apaSq0qqfCSGmyF1SSUjCSP1lzwk12S3FBqS6l0Eq2ALxVlFNh2ka2panVzDTsCF1sucuxHqDdmtBXy2AHHVaV17b6v-JsVy38UzUrmcpeZwDdAprgYwxgdr2UVOvIql1k1Xtkuef049Bdx7-MsuBsK_Dj8hO8v-4Xro8</recordid><startdate>20200514</startdate><enddate>20200514</enddate><creator>Sama, Iziah E</creator><creator>Ravera, Alice</creator><creator>Santema, Bernadet T</creator><creator>van Goor, Harry</creator><creator>ter Maaten, Jozine M</creator><creator>Cleland, John G F</creator><creator>Rienstra, Michiel</creator><creator>Friedrich, Alex W</creator><creator>Samani, Nilesh J</creator><creator>Ng, Leong L</creator><creator>Dickstein, Kenneth</creator><creator>Lang, Chim C</creator><creator>Filippatos, Gerasimos</creator><creator>Anker, Stefan D</creator><creator>Ponikowski, Piotr</creator><creator>Metra, Marco</creator><creator>van Veldhuisen, Dirk J</creator><creator>Voors, Adriaan A</creator><general>Oxford University Press</general><scope>TOX</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2581-070X</orcidid><orcidid>https://orcid.org/0000-0002-6553-5749</orcidid><orcidid>https://orcid.org/0000-0002-4663-7213</orcidid><orcidid>https://orcid.org/0000-0003-3331-7314</orcidid><orcidid>https://orcid.org/0000-0002-5417-4415</orcidid></search><sort><creationdate>20200514</creationdate><title>Circulating plasma concentrations of angiotensin-converting enzyme 2 in men and women with heart failure and effects of renin–angiotensin–aldosterone inhibitors</title><author>Sama, Iziah E ; Ravera, Alice ; Santema, Bernadet T ; van Goor, Harry ; ter Maaten, Jozine M ; Cleland, John G F ; Rienstra, Michiel ; Friedrich, Alex W ; Samani, Nilesh J ; Ng, Leong L ; Dickstein, Kenneth ; Lang, Chim C ; Filippatos, Gerasimos ; Anker, Stefan D ; Ponikowski, Piotr ; Metra, Marco ; van Veldhuisen, Dirk J ; Voors, Adriaan A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c394t-a9b46f88faa31802630856b505f09395611a286a98dee5d91516fdc8d2fb97fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aged</topic><topic>Angiotensin Receptor Antagonists - therapeutic use</topic><topic>Angiotensin-Converting Enzyme 2</topic><topic>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</topic><topic>Betacoronavirus</topic><topic>Coronavirus Infections</topic><topic>COVID-19</topic><topic>Editor's Choice</topic><topic>Europe</topic><topic>Fast Track Clinical Research</topic><topic>Female</topic><topic>Heart Failure - blood</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mineralocorticoid Receptor Antagonists - therapeutic use</topic><topic>Pandemics</topic><topic>Peptidyl-Dipeptidase A - blood</topic><topic>Pneumonia, Viral</topic><topic>Renin-Angiotensin System - drug effects</topic><topic>SARS-CoV-2</topic><topic>Sex Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sama, Iziah E</creatorcontrib><creatorcontrib>Ravera, Alice</creatorcontrib><creatorcontrib>Santema, Bernadet T</creatorcontrib><creatorcontrib>van Goor, Harry</creatorcontrib><creatorcontrib>ter Maaten, Jozine M</creatorcontrib><creatorcontrib>Cleland, John G F</creatorcontrib><creatorcontrib>Rienstra, Michiel</creatorcontrib><creatorcontrib>Friedrich, Alex W</creatorcontrib><creatorcontrib>Samani, Nilesh J</creatorcontrib><creatorcontrib>Ng, Leong L</creatorcontrib><creatorcontrib>Dickstein, Kenneth</creatorcontrib><creatorcontrib>Lang, Chim C</creatorcontrib><creatorcontrib>Filippatos, Gerasimos</creatorcontrib><creatorcontrib>Anker, Stefan D</creatorcontrib><creatorcontrib>Ponikowski, Piotr</creatorcontrib><creatorcontrib>Metra, Marco</creatorcontrib><creatorcontrib>van Veldhuisen, Dirk J</creatorcontrib><creatorcontrib>Voors, Adriaan A</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>European heart journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sama, Iziah E</au><au>Ravera, Alice</au><au>Santema, Bernadet T</au><au>van Goor, Harry</au><au>ter Maaten, Jozine M</au><au>Cleland, John G F</au><au>Rienstra, Michiel</au><au>Friedrich, Alex W</au><au>Samani, Nilesh J</au><au>Ng, Leong L</au><au>Dickstein, Kenneth</au><au>Lang, Chim C</au><au>Filippatos, Gerasimos</au><au>Anker, Stefan D</au><au>Ponikowski, Piotr</au><au>Metra, Marco</au><au>van Veldhuisen, Dirk J</au><au>Voors, Adriaan A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Circulating plasma concentrations of angiotensin-converting enzyme 2 in men and women with heart failure and effects of renin–angiotensin–aldosterone inhibitors</atitle><jtitle>European heart journal</jtitle><addtitle>Eur Heart J</addtitle><date>2020-05-14</date><risdate>2020</risdate><volume>41</volume><issue>19</issue><spage>1810</spage><epage>1817</epage><pages>1810-1817</pages><issn>0195-668X</issn><eissn>1522-9645</eissn><abstract>Abstract
Aims
The current pandemic coronavirus SARS-CoV-2 infects a wide age group but predominantly elderly individuals, especially men and those with cardiovascular disease. Recent reports suggest an association with use of renin–angiotensin–aldosterone system (RAAS) inhibitors. Angiotensin-converting enzyme 2 (ACE2) is a functional receptor for coronaviruses. Higher ACE2 concentrations might lead to increased vulnerability to SARS-CoV-2 in patients on RAAS inhibitors.
Methods and results
We measured ACE2 concentrations in 1485 men and 537 women with heart failure (index cohort). Results were validated in 1123 men and 575 women (validation cohort).
The median age was 69 years for men and 75 years for women. The strongest predictor of elevated concentrations of ACE2 in both cohorts was male sex (estimate = 0.26, P < 0.001; and 0.19, P < 0.001, respectively). In the index cohort, use of ACE inhibitors, angiotensin receptor blockers (ARBs), or mineralocorticoid receptor antagonists (MRAs) was not an independent predictor of plasma ACE2. In the validation cohort, ACE inhibitor (estimate = –0.17, P = 0.002) and ARB use (estimate = –0.15, P = 0.03) were independent predictors of lower plasma ACE2, while use of an MRA (estimate = 0.11, P = 0.04) was an independent predictor of higher plasma ACE2 concentrations.
Conclusion
In two independent cohorts of patients with heart failure, plasma concentrations of ACE2 were higher in men than in women, but use of neither an ACE inhibitor nor an ARB was associated with higher plasma ACE2 concentrations. These data might explain the higher incidence and fatality rate of COVID-19 in men, but do not support previous reports suggesting that ACE inhibitors or ARBs increase the vulnerability for COVID-19 through increased plasma ACE2 concentrations.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>32388565</pmid><doi>10.1093/eurheartj/ehaa373</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-2581-070X</orcidid><orcidid>https://orcid.org/0000-0002-6553-5749</orcidid><orcidid>https://orcid.org/0000-0002-4663-7213</orcidid><orcidid>https://orcid.org/0000-0003-3331-7314</orcidid><orcidid>https://orcid.org/0000-0002-5417-4415</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aged Angiotensin Receptor Antagonists - therapeutic use Angiotensin-Converting Enzyme 2 Angiotensin-Converting Enzyme Inhibitors - therapeutic use Betacoronavirus Coronavirus Infections COVID-19 Editor's Choice Europe Fast Track Clinical Research Female Heart Failure - blood Humans Male Middle Aged Mineralocorticoid Receptor Antagonists - therapeutic use Pandemics Peptidyl-Dipeptidase A - blood Pneumonia, Viral Renin-Angiotensin System - drug effects SARS-CoV-2 Sex Factors |
title | Circulating plasma concentrations of angiotensin-converting enzyme 2 in men and women with heart failure and effects of renin–angiotensin–aldosterone inhibitors |
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