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Renin-Angiotensin System Blocker in COVID-19. A Single Center Study
Riya Job1, Mohamed Abdul Qader1, Pedro Torres1
1Departments of Medicine; and.
Abstract:
Early during the Coronavirus disease 2019 (Covid-19) pandemic, concerns were raised regarding potential adverse outcomes in patients taking angiotensin-converting enzyme inhibitors (ACEIs)/angiotensin receptor blockers (ARBs). These concerns were based on animal studies showing increased ACE-2 expression in mice treated with ACEI/ARB. This is a single-center, retrospective, cohort study of 289 patients diagnosed with 2019 Novel Coronavirus (SARS-CoV-2) hospitalized between March of 2020 and June of 2020. The study was intended to investigate the impact of ACEIs and/or ARBs on in-hospital mortality, intensive care unit (ICU) admission, postadmission hemodialysis requirement, and the need for mechanical ventilation in patients with COVID-19. This cohort of 289 patients included 139 of 289 women (48%) with a mean age of 61 ± 19 years. Patients using ACEIs/ARBs were older (69.68 vs. 57.9 years; P < 0.0001), more likely to have a history of hypertension (97% vs. 36%; P < 0.0001), diabetes mellitus (48% vs. 20.9%; P < 0.0001), chronic heart failure (11.39% vs. 4.29%; P < 0.0512), coronary artery disease (20.25% vs. 7.14%; P < 0.0025), stroke/Transient Ischemic Attack (7.59% vs. 2.38%; P < 0.0761), chronic kidney disease (11.39% vs. 3.33%; P < 0.0167), atrial fibrillation/flutter (18.99% vs. 7.14%; P < 0.0080), and dementia (22.7% vs. 11.4%; P < 0.0233) compared with the nonuser group. There was significantly higher in-hospital mortality in patients using ACEIs/ARBs than nonusers, respectively (32.9% vs. 15.2%; P < 0.0015). However, a multivariate logistics regression analysis performed to adjust for common confounders demonstrated no significant difference in all-cause in-patient mortality (P 0.7141). Admission to ICU, postadmission hemodialysis requirement, and mechanical ventilation showed no significant differences between the 2 groups (P = NS). This study suggests that the use of ACEIs and ARBs in patients with COVID-19 was not found to significantly increase all-cause in-hospital mortality, ICU admissions, and hemodialysis and mechanical ventilation requirements.
Insights
This study found that angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) did not significantly increase mortality or critical care needs in COVID-19 patients. These findings address early pandemic concerns about ACEI/ARB use in SARS-CoV-2 patients.
Area of Science:
- Cardiology
- Infectious Diseases
- Pharmacology
Background:
- Early COVID-19 pandemic concerns arose regarding potential adverse effects of ACEIs/ARBs.
- Concerns were linked to animal studies showing increased ACE-2 expression with ACEI/ARB treatment.
- This study aimed to clarify the impact of these medications on COVID-19 patient outcomes.
Purpose of the Study:
- To investigate the association between ACEI/ARB use and in-hospital mortality in COVID-19 patients.
- To assess the impact of ACEI/ARB use on ICU admission, hemodialysis, and mechanical ventilation requirements.
- To determine if ACEI/ARB use is associated with worse outcomes in hospitalized SARS-CoV-2 patients.
Main Methods:
- Retrospective cohort study of 289 hospitalized COVID-19 patients.
- Comparison of outcomes between patients using ACEIs/ARBs and non-users.
- Multivariate logistic regression analysis to adjust for confounding factors.
Main Results:
- Unadjusted analysis showed higher mortality in ACEI/ARB users (32.9% vs. 15.2%).
- Multivariate analysis revealed no significant difference in all-cause in-hospital mortality (P=0.7141).
- No significant differences were observed in ICU admission, hemodialysis, or mechanical ventilation rates between groups.
Conclusions:
- ACEI/ARB use in COVID-19 patients was not associated with increased all-cause in-hospital mortality after adjusting for confounders.
- The study suggests that ACEIs and ARBs do not significantly worsen critical outcomes in hospitalized COVID-19 patients.
- Findings help alleviate early pandemic-related concerns about these commonly prescribed medications.
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