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ACEI/ARB use and risk of infection or severity or mortality of COVID-19: A systematic review and meta-analysis
The effects of angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) on the risk of COVID-19 infection and disease progression are yet to be investigated. The relationship between ACEI/ARB use and COVID-19 infection was systematically reviewed. To identify relevan...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7227582/ https://www.ncbi.nlm.nih.gov/pubmed/32422341 http://dx.doi.org/10.1016/j.phrs.2020.104927 |
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author | Zhang, Xue Yu, Jiong Pan, Li-ya Jiang, Hai-yin |
author_facet | Zhang, Xue Yu, Jiong Pan, Li-ya Jiang, Hai-yin |
author_sort | Zhang, Xue |
collection | PubMed |
description | The effects of angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) on the risk of COVID-19 infection and disease progression are yet to be investigated. The relationship between ACEI/ARB use and COVID-19 infection was systematically reviewed. To identify relevant studies that met predetermined inclusion criteria, unrestricted searches of the PubMed, Embase, and Cochrane Library databases were conducted. The search strategy included clinical date published until May 9, 2020. Twelve articles involving more than 19,000 COVID-19 cases were included. To estimate overall risk, random-effects models were adopted. Our results showed that ACEI/ARB exposure was not associated with a higher risk of COVID-19 infection (OR = 0.99; 95 % CI, 0–1.04; P = 0.672). Among those with COVID-19 infection, ACEI/ARB exposure was also not associated with a higher risk of having severe infection (OR = 0.98; 95 % CI, 0.87–1.09; P = 0.69) or mortality (OR = 0.73, 95 %CI, 0.5–1.07; P = 0.111). However, ACEI/ARB exposure was associated with a lower risk of mortality compared to those on non-ACEI/ARB antihypertensive drugs (OR = 0.48, 95 % CI, 0.29−0.81; P = 0.006). In conclusion, current evidence did not confirm the concern that ACEI/ARB exposure is harmful in patientswith COVID-19 infection. This study supports the current guidelines that discourage discontinuation of ACEIs or ARBs in COVID-19 patients and the setting of the COVID-19 pandemic. |
format | Online Article Text |
id | pubmed-7227582 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72275822020-05-18 ACEI/ARB use and risk of infection or severity or mortality of COVID-19: A systematic review and meta-analysis Zhang, Xue Yu, Jiong Pan, Li-ya Jiang, Hai-yin Pharmacol Res Article The effects of angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) on the risk of COVID-19 infection and disease progression are yet to be investigated. The relationship between ACEI/ARB use and COVID-19 infection was systematically reviewed. To identify relevant studies that met predetermined inclusion criteria, unrestricted searches of the PubMed, Embase, and Cochrane Library databases were conducted. The search strategy included clinical date published until May 9, 2020. Twelve articles involving more than 19,000 COVID-19 cases were included. To estimate overall risk, random-effects models were adopted. Our results showed that ACEI/ARB exposure was not associated with a higher risk of COVID-19 infection (OR = 0.99; 95 % CI, 0–1.04; P = 0.672). Among those with COVID-19 infection, ACEI/ARB exposure was also not associated with a higher risk of having severe infection (OR = 0.98; 95 % CI, 0.87–1.09; P = 0.69) or mortality (OR = 0.73, 95 %CI, 0.5–1.07; P = 0.111). However, ACEI/ARB exposure was associated with a lower risk of mortality compared to those on non-ACEI/ARB antihypertensive drugs (OR = 0.48, 95 % CI, 0.29−0.81; P = 0.006). In conclusion, current evidence did not confirm the concern that ACEI/ARB exposure is harmful in patientswith COVID-19 infection. This study supports the current guidelines that discourage discontinuation of ACEIs or ARBs in COVID-19 patients and the setting of the COVID-19 pandemic. Elsevier Ltd. 2020-08 2020-05-15 /pmc/articles/PMC7227582/ /pubmed/32422341 http://dx.doi.org/10.1016/j.phrs.2020.104927 Text en © 2020 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Zhang, Xue Yu, Jiong Pan, Li-ya Jiang, Hai-yin ACEI/ARB use and risk of infection or severity or mortality of COVID-19: A systematic review and meta-analysis |
title | ACEI/ARB use and risk of infection or severity or mortality of COVID-19: A systematic review and meta-analysis |
title_full | ACEI/ARB use and risk of infection or severity or mortality of COVID-19: A systematic review and meta-analysis |
title_fullStr | ACEI/ARB use and risk of infection or severity or mortality of COVID-19: A systematic review and meta-analysis |
title_full_unstemmed | ACEI/ARB use and risk of infection or severity or mortality of COVID-19: A systematic review and meta-analysis |
title_short | ACEI/ARB use and risk of infection or severity or mortality of COVID-19: A systematic review and meta-analysis |
title_sort | acei/arb use and risk of infection or severity or mortality of covid-19: a systematic review and meta-analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7227582/ https://www.ncbi.nlm.nih.gov/pubmed/32422341 http://dx.doi.org/10.1016/j.phrs.2020.104927 |
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