Angiotensin II receptor blocker or angiotensin-converting enzyme inhibitor use and COVID-19-related outcomes among US Veterans

Author:

Derington Catherine G.,Cohen Jordana B.,Mohanty April F.ORCID,Greene Tom H.,Cook James,Ying Jian,Wei Guo,Herrick Jennifer S.,Stevens Vanessa W.,Jones Barbara E.,Wang LiboORCID,Zheutlin Alexander R.,South Andrew M.ORCID,Hanff Thomas C.ORCID,Smith Steven M.ORCID,Cooper-DeHoff Rhonda M.,King Jordan B.ORCID,Alexander G. Caleb,Berlowitz Dan R.,Ahmad Faraz S.,Penrod M. Jason,Hess RachelORCID,Conroy Molly B.,Fang James C.,Rubin Michael A.,Beddhu Srinivasan,Cheung Alfred K.,Xian Weiming,Weintraub William S.,Bress Adam P.ORCID

Abstract

Background Angiotensin II receptor blockers (ARBs) and angiotensin-converting enzyme inhibitors (ACEIs) may positively or negatively impact outcomes in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. We investigated the association of ARB or ACEI use with coronavirus disease 2019 (COVID-19)-related outcomes in US Veterans with treated hypertension using an active comparator design, appropriate covariate adjustment, and negative control analyses. Methods and findings In this retrospective cohort study of Veterans with treated hypertension in the Veterans Health Administration (01/19/2020-08/28/2020), we compared users of (A) ARB/ACEI vs. non-ARB/ACEI (excluding Veterans with compelling indications to reduce confounding by indication) and (B) ARB vs. ACEI among (1) SARS-CoV-2+ outpatients and (2) COVID-19 hospitalized inpatients. The primary outcome was all-cause hospitalization or mortality (outpatients) and all-cause mortality (inpatients). We estimated hazard ratios (HR) using propensity score-weighted Cox regression. Baseline characteristics were well-balanced between exposure groups after weighting. Among outpatients, there were 5.0 and 6.0 primary outcomes per 100 person-months for ARB/ACEI (n = 2,482) vs. non-ARB/ACEI (n = 2,487) users (HR 0.85, 95% confidence interval [CI] 0.73–0.99, median follow-up 87 days). Among outpatients who were ARB (n = 4,877) vs. ACEI (n = 8,704) users, there were 13.2 and 14.8 primary outcomes per 100 person-months (HR 0.91, 95%CI 0.86–0.97, median follow-up 85 days). Among inpatients who were ARB/ACEI (n = 210) vs. non-ARB/ACEI (n = 275) users, there were 3.4 and 2.0 all-cause deaths per 100 person months (HR 1.25, 95%CI 0.30–5.13, median follow-up 30 days). Among inpatients, ARB (n = 1,164) and ACEI (n = 2,014) users had 21.0 vs. 17.7 all-cause deaths, per 100 person-months (HR 1.13, 95%CI 0.93–1.38, median follow-up 30 days). Conclusions This observational analysis supports continued ARB or ACEI use for patients already using these medications before SARS-CoV-2 infection. The novel beneficial association observed among outpatients between users of ARBs vs. ACEIs on hospitalization or mortality should be confirmed with randomized trials.

Funder

National Heart, Lung and Blood Institute

National Center for Research Resources and the National Center for Advancing Translational Sciences, National Institutes of Health

National Institute on Aging

Veterans Health Administration-Office of Health Services Research and Development, Career Development

National Institutes of Health

Patient-Centered Outcomes Research Institute

VA Informatics and Computing Infrastructure

American Heart Association

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

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