Serveur d'exploration sur la COVID en France

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The Effects of ARBs, ACEis, and Statins on Clinical Outcomes of COVID-19 Infection Among Nursing Home Residents.

Identifieur interne : 000474 ( Main/Exploration ); précédent : 000473; suivant : 000475

The Effects of ARBs, ACEis, and Statins on Clinical Outcomes of COVID-19 Infection Among Nursing Home Residents.

Auteurs : Anton De Spiegeleer [Belgique] ; Antoon Bronselaer [Belgique] ; James T. Teo [Royaume-Uni] ; Geert Byttebier [Belgique] ; Guy De Tré [Belgique] ; Luc Belmans [Belgique] ; Richard Dobson [Royaume-Uni] ; Evelien Wynendaele [Belgique] ; Christophe Van De Wiele [Belgique] ; Filip Vandaele [Belgique] ; Diemer Van Dijck [Belgique] ; Dan Bean [Royaume-Uni] ; David Fedson [France] ; Bart De Spiegeleer [Belgique]

Source :

RBID : pubmed:32674818

Descripteurs français

English descriptors

Abstract

OBJECTIVES

Angiotensin-converting enzyme inhibitors (ACEi), angiotensin II receptor blockers (ARBs), and HMG-CoA reductase inhibitors ("statins") have been hypothesized to affect COVID-19 severity. However, up to now, no studies investigating this association have been conducted in the most vulnerable and affected population groups (ie, older adults residing in nursing homes). The objective of this study was to explore the association of ACEi/ARB and/or statins with clinical manifestations in COVID-19-infected older adults residing in nursing homes.

DESIGN

We undertook a retrospective multicenter cohort study to analyze the association between ACEi/ARB and/or statin use with clinical outcome of COVID-19. The outcomes were (1) serious COVID-19 defined as long-stay hospital admission or death within 14 days of disease onset, and (2) asymptomatic (ie, no disease symptoms in the whole study period while still being diagnosed by polymerase chain reaction).

SETTING AND PARTICIPANTS

A total of 154 COVID-19-positive subjects were identified, residing in 1 of 2 Belgian nursing homes that experienced similar COVID-19 outbreaks.

MEASURES

Logistic regression models were applied with age, sex, functional status, diabetes, and hypertension as covariates.

RESULTS

We found a statistically significant association between statin intake and the absence of symptoms during COVID-19 (odds ratio [OR] 2.91; confidence interval [CI] 1.27-6.71), which remained statistically significant after adjusting for covariates (OR 2.65; CI 1.13-6.68). Although the effects of statin intake on serious clinical outcome were in the same beneficial direction, these were not statistically significant (OR 0.75; CI 0.24-1.87). There was also no statistically significant association between ACEi/ARB and asymptomatic status (OR 2.72; CI 0.59-25.1) or serious clinical outcome (OR 0.48; CI 0.10-1.97).

CONCLUSIONS AND IMPLICATIONS

Our data indicate that statin intake in older, frail adults could be associated with a considerable beneficial effect on COVID-19 clinical symptoms. The role of statins and renin-angiotensin system drugs needs to be further explored in larger observational studies as well as randomized clinical trials.


DOI: 10.1016/j.jamda.2020.06.018
PubMed: 32674818
PubMed Central: PMC7294267


Affiliations:


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Le document en format XML

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<title level="j">Journal of the American Medical Directors Association</title>
<idno type="eISSN">1538-9375</idno>
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<date when="2020" type="published">2020</date>
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<term>Aged (MeSH)</term>
<term>Aged, 80 and over (MeSH)</term>
<term>Angiotensin Receptor Antagonists (administration & dosage)</term>
<term>Angiotensin-Converting Enzyme Inhibitors (administration & dosage)</term>
<term>Belgium (epidemiology)</term>
<term>Cause of Death (MeSH)</term>
<term>Cohort Studies (MeSH)</term>
<term>Coronavirus Infections (drug therapy)</term>
<term>Coronavirus Infections (epidemiology)</term>
<term>Female (MeSH)</term>
<term>Geriatric Assessment (MeSH)</term>
<term>Homes for the Aged (statistics & numerical data)</term>
<term>Humans (MeSH)</term>
<term>Hydroxymethylglutaryl-CoA Reductase Inhibitors (administration & dosage)</term>
<term>Logistic Models (MeSH)</term>
<term>Male (MeSH)</term>
<term>Nursing Homes (statistics & numerical data)</term>
<term>Odds Ratio (MeSH)</term>
<term>Pandemics (statistics & numerical data)</term>
<term>Pneumonia, Viral (drug therapy)</term>
<term>Pneumonia, Viral (epidemiology)</term>
<term>Retrospective Studies (MeSH)</term>
<term>Risk Assessment (MeSH)</term>
<term>Severity of Illness Index (MeSH)</term>
<term>Survival Rate (MeSH)</term>
<term>Treatment Outcome (MeSH)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Antagonistes des récepteurs aux angiotensines (administration et posologie)</term>
<term>Appréciation des risques (MeSH)</term>
<term>Belgique (épidémiologie)</term>
<term>Cause de décès (MeSH)</term>
<term>Femelle (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Indice de gravité de la maladie (MeSH)</term>
<term>Infections à coronavirus (traitement médicamenteux)</term>
<term>Infections à coronavirus (épidémiologie)</term>
<term>Inhibiteurs de l'enzyme de conversion de l'angiotensine (administration et posologie)</term>
<term>Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase (administration et posologie)</term>
<term>Maisons de repos (statistiques et données numériques)</term>
<term>Maisons de retraite médicalisées (statistiques et données numériques)</term>
<term>Modèles logistiques (MeSH)</term>
<term>Mâle (MeSH)</term>
<term>Odds ratio (MeSH)</term>
<term>Pandémies (statistiques et données numériques)</term>
<term>Pneumopathie virale (traitement médicamenteux)</term>
<term>Pneumopathie virale (épidémiologie)</term>
<term>Résultat thérapeutique (MeSH)</term>
<term>Sujet âgé (MeSH)</term>
<term>Sujet âgé de 80 ans ou plus (MeSH)</term>
<term>Taux de survie (MeSH)</term>
<term>Études de cohortes (MeSH)</term>
<term>Études rétrospectives (MeSH)</term>
<term>Évaluation gériatrique (MeSH)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="administration & dosage" xml:lang="en">
<term>Angiotensin Receptor Antagonists</term>
<term>Angiotensin-Converting Enzyme Inhibitors</term>
<term>Hydroxymethylglutaryl-CoA Reductase Inhibitors</term>
</keywords>
<keywords scheme="MESH" type="geographic" qualifier="epidemiology" xml:lang="en">
<term>Belgium</term>
</keywords>
<keywords scheme="MESH" qualifier="administration et posologie" xml:lang="fr">
<term>Antagonistes des récepteurs aux angiotensines</term>
<term>Inhibiteurs de l'enzyme de conversion de l'angiotensine</term>
<term>Inhibiteurs de l'hydroxyméthylglutaryl-CoA réductase</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en">
<term>Coronavirus Infections</term>
<term>Pneumonia, Viral</term>
</keywords>
<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en">
<term>Coronavirus Infections</term>
<term>Pneumonia, Viral</term>
</keywords>
<keywords scheme="MESH" qualifier="statistics & numerical data" xml:lang="en">
<term>Homes for the Aged</term>
<term>Nursing Homes</term>
<term>Pandemics</term>
</keywords>
<keywords scheme="MESH" qualifier="statistiques et données numériques" xml:lang="fr">
<term>Maisons de repos</term>
<term>Maisons de retraite médicalisées</term>
<term>Pandémies</term>
</keywords>
<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr">
<term>Infections à coronavirus</term>
<term>Pneumopathie virale</term>
</keywords>
<keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr">
<term>Belgique</term>
<term>Infections à coronavirus</term>
<term>Pneumopathie virale</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Cause of Death</term>
<term>Cohort Studies</term>
<term>Female</term>
<term>Geriatric Assessment</term>
<term>Humans</term>
<term>Logistic Models</term>
<term>Male</term>
<term>Odds Ratio</term>
<term>Retrospective Studies</term>
<term>Risk Assessment</term>
<term>Severity of Illness Index</term>
<term>Survival Rate</term>
<term>Treatment Outcome</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Appréciation des risques</term>
<term>Cause de décès</term>
<term>Femelle</term>
<term>Humains</term>
<term>Indice de gravité de la maladie</term>
<term>Modèles logistiques</term>
<term>Mâle</term>
<term>Odds ratio</term>
<term>Résultat thérapeutique</term>
<term>Sujet âgé</term>
<term>Sujet âgé de 80 ans ou plus</term>
<term>Taux de survie</term>
<term>Études de cohortes</term>
<term>Études rétrospectives</term>
<term>Évaluation gériatrique</term>
</keywords>
<keywords scheme="Wicri" type="geographic" xml:lang="fr">
<term>Belgique</term>
</keywords>
</textClass>
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</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p>
<b>OBJECTIVES</b>
</p>
<p>Angiotensin-converting enzyme inhibitors (ACEi), angiotensin II receptor blockers (ARBs), and HMG-CoA reductase inhibitors ("statins") have been hypothesized to affect COVID-19 severity. However, up to now, no studies investigating this association have been conducted in the most vulnerable and affected population groups (ie, older adults residing in nursing homes). The objective of this study was to explore the association of ACEi/ARB and/or statins with clinical manifestations in COVID-19-infected older adults residing in nursing homes.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>DESIGN</b>
</p>
<p>We undertook a retrospective multicenter cohort study to analyze the association between ACEi/ARB and/or statin use with clinical outcome of COVID-19. The outcomes were (1) serious COVID-19 defined as long-stay hospital admission or death within 14 days of disease onset, and (2) asymptomatic (ie, no disease symptoms in the whole study period while still being diagnosed by polymerase chain reaction).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>SETTING AND PARTICIPANTS</b>
</p>
<p>A total of 154 COVID-19-positive subjects were identified, residing in 1 of 2 Belgian nursing homes that experienced similar COVID-19 outbreaks.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>MEASURES</b>
</p>
<p>Logistic regression models were applied with age, sex, functional status, diabetes, and hypertension as covariates.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>We found a statistically significant association between statin intake and the absence of symptoms during COVID-19 (odds ratio [OR] 2.91; confidence interval [CI] 1.27-6.71), which remained statistically significant after adjusting for covariates (OR 2.65; CI 1.13-6.68). Although the effects of statin intake on serious clinical outcome were in the same beneficial direction, these were not statistically significant (OR 0.75; CI 0.24-1.87). There was also no statistically significant association between ACEi/ARB and asymptomatic status (OR 2.72; CI 0.59-25.1) or serious clinical outcome (OR 0.48; CI 0.10-1.97).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS AND IMPLICATIONS</b>
</p>
<p>Our data indicate that statin intake in older, frail adults could be associated with a considerable beneficial effect on COVID-19 clinical symptoms. The role of statins and renin-angiotensin system drugs needs to be further explored in larger observational studies as well as randomized clinical trials.</p>
</div>
</front>
</TEI>
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<Year>2020</Year>
<Month>07</Month>
<Day>30</Day>
</DateCompleted>
<DateRevised>
<Year>2020</Year>
<Month>07</Month>
<Day>30</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">1538-9375</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>21</Volume>
<Issue>7</Issue>
<PubDate>
<Year>2020</Year>
<Month>Jul</Month>
</PubDate>
</JournalIssue>
<Title>Journal of the American Medical Directors Association</Title>
<ISOAbbreviation>J Am Med Dir Assoc</ISOAbbreviation>
</Journal>
<ArticleTitle>The Effects of ARBs, ACEis, and Statins on Clinical Outcomes of COVID-19 Infection Among Nursing Home Residents.</ArticleTitle>
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<AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">Angiotensin-converting enzyme inhibitors (ACEi), angiotensin II receptor blockers (ARBs), and HMG-CoA reductase inhibitors ("statins") have been hypothesized to affect COVID-19 severity. However, up to now, no studies investigating this association have been conducted in the most vulnerable and affected population groups (ie, older adults residing in nursing homes). The objective of this study was to explore the association of ACEi/ARB and/or statins with clinical manifestations in COVID-19-infected older adults residing in nursing homes.</AbstractText>
<AbstractText Label="DESIGN" NlmCategory="METHODS">We undertook a retrospective multicenter cohort study to analyze the association between ACEi/ARB and/or statin use with clinical outcome of COVID-19. The outcomes were (1) serious COVID-19 defined as long-stay hospital admission or death within 14 days of disease onset, and (2) asymptomatic (ie, no disease symptoms in the whole study period while still being diagnosed by polymerase chain reaction).</AbstractText>
<AbstractText Label="SETTING AND PARTICIPANTS" NlmCategory="METHODS">A total of 154 COVID-19-positive subjects were identified, residing in 1 of 2 Belgian nursing homes that experienced similar COVID-19 outbreaks.</AbstractText>
<AbstractText Label="MEASURES" NlmCategory="METHODS">Logistic regression models were applied with age, sex, functional status, diabetes, and hypertension as covariates.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">We found a statistically significant association between statin intake and the absence of symptoms during COVID-19 (odds ratio [OR] 2.91; confidence interval [CI] 1.27-6.71), which remained statistically significant after adjusting for covariates (OR 2.65; CI 1.13-6.68). Although the effects of statin intake on serious clinical outcome were in the same beneficial direction, these were not statistically significant (OR 0.75; CI 0.24-1.87). There was also no statistically significant association between ACEi/ARB and asymptomatic status (OR 2.72; CI 0.59-25.1) or serious clinical outcome (OR 0.48; CI 0.10-1.97).</AbstractText>
<AbstractText Label="CONCLUSIONS AND IMPLICATIONS" NlmCategory="CONCLUSIONS">Our data indicate that statin intake in older, frail adults could be associated with a considerable beneficial effect on COVID-19 clinical symptoms. The role of statins and renin-angiotensin system drugs needs to be further explored in larger observational studies as well as randomized clinical trials.</AbstractText>
<CopyrightInformation>Copyright © 2020 AMDA – The Society for Post-Acute and Long-Term Care Medicine. All rights reserved.</CopyrightInformation>
</Abstract>
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<LastName>De Spiegeleer</LastName>
<ForeName>Anton</ForeName>
<Initials>A</Initials>
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<Affiliation>Drug Quality and Registration Group, Faculty of Pharmaceutical Sciences, Ghent University, Ghent, Belgium; Department of Geriatrics, Faculty of Medicine and Health Sciences, Ghent University Hospital, Ghent, Belgium; Unit for Molecular Immunology and Inflammation, VIB-Center for Inflammation Research, Ghent, Belgium.</Affiliation>
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<Affiliation>DDCM Laboratory, Department of Telecommunications and Information Processing, Faculty of Engineering and Architecture, Ghent University, Ghent, Belgium.</Affiliation>
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<LastName>Teo</LastName>
<ForeName>James T</ForeName>
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<Affiliation>Department of Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.</Affiliation>
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<ForeName>Geert</ForeName>
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<ForeName>Guy</ForeName>
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<LastName>Belmans</LastName>
<ForeName>Luc</ForeName>
<Initials>L</Initials>
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<Affiliation>Department of Public Health and Primary Care, Faculty of Medicine and Health Sciences, Ghent University Hospital, Ghent, Belgium.</Affiliation>
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<ForeName>Filip</ForeName>
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<ForeName>Diemer</ForeName>
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<LastName>Fedson</LastName>
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<ForeName>Bart</ForeName>
<Initials>B</Initials>
<AffiliationInfo>
<Affiliation>Drug Quality and Registration Group, Faculty of Pharmaceutical Sciences, Ghent University, Ghent, Belgium. Electronic address: bart.despiegeleer@ugent.be.</Affiliation>
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<Month>06</Month>
<Day>15</Day>
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