Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Observational Study
. 2021 Jul;16(7):1061-1072.
doi: 10.2215/CJN.18961220. Epub 2021 Jun 4.

Renin-Angiotensin System Blockers and the Risk of COVID-19-Related Mortality in Patients with Kidney Failure

Collaborators, Affiliations
Observational Study

Renin-Angiotensin System Blockers and the Risk of COVID-19-Related Mortality in Patients with Kidney Failure

Maria Jose Soler et al. Clin J Am Soc Nephrol. 2021 Jul.

Abstract

Background and objectives: There is concern about potential deleterious effects of angiotensin-converting enzyme inhibitors (ACEis) and angiotensin II receptor blockers (ARBs) in patients with coronavirus disease 2019 (COVID-19). Patients with kidney failure, who often use ACEis/ARBs, are at higher risk of more severe COVID-19. However, there are no data available on the association of ACEi/ARB use with COVID-19 severity in this population.

Design, setting, participants, & measurements: From the European Renal Association COVID-19 database (ERACODA), we retrieved data on kidney transplant recipients and patients on dialysis who were affected by COVID-19, between February 1 and October 1, 2020, and had information on 28-day mortality. We used Cox proportional-hazards regression to calculate hazard ratios for the association between ACEi/ARB use and 28-day mortality risk. Additionally, we studied the association of discontinuation of these agents with 28-day mortality.

Results: We evaluated 1511 patients: 459 kidney transplant recipients and 1052 patients on dialysis. At diagnosis of COVID-19, 189 (41%) of the transplant recipients and 288 (27%) of the patients on dialysis were on ACEis/ARBs. A total of 88 (19%) transplant recipients and 244 (23%) patients on dialysis died within 28 days of initial presentation. In both groups of patients, there was no association between ACEi/ARB use and 28-day mortality in both crude and adjusted models (in transplant recipients, adjusted hazard ratio, 1.12; 95% confidence interval [95% CI], 0.69 to 1.83; in patients on dialysis, adjusted hazard ratio, 1.04; 95% CI, 0.73 to 1.47). Among transplant recipients, ACEi/ARB discontinuation was associated with a higher mortality risk after adjustment for demographics and comorbidities, but the association was no longer statistically significant after adjustment for severity of COVID-19 (adjusted hazard ratio, 1.36; 95% CI, 0.40 to 4.58). Among patients on dialysis, ACEi/ARB discontinuation was not associated with mortality in any model. We obtained similar results across subgroups when ACEis and ARBs were studied separately, and when other outcomes for severity of COVID-19 were studied, e.g., hospital admission, admission to the intensive care unit, or need for ventilator support.

Conclusions: Among kidney transplant recipients and patients on dialysis with COVID-19, there was no significant association of ACEi/ARB use or discontinuation with mortality.

Keywords: COVID-19; dialysis; kidney failure; kidney transplantation; renin angiotensin system.

PubMed Disclaimer

Figures

None
Graphical abstract
Figure 1.
Figure 1.
Cumulative survival probability in transplant recipients and patients on dialysis among those using (users) and those not using (nonusers) angiotensin-converting enzyme inhibitors/angiotensin II receptor blockers. (A) transplant recipients, (B) patients on dialysis.
Figure 2.
Figure 2.
Distribution of (A) hospitalization, (B) admission to the intensive care unit, and (C) ventilator support in patients on dialysis and transplant recipients by use of angiotensin-converting enzyme inhibitors/angiotensin II receptor blockers.

Similar articles

Cited by

References

    1. Soler MJ, Barrios C, Oliva R, Batlle D: Pharmacologic modulation of ACE2 expression. Curr Hypertens Rep 10: 410–414, 2008 - PMC - PubMed
    1. Soler MJ, Ye M, Wysocki J, William J, Lloveras J, Batlle D: Localization of ACE2 in the renal vasculature: Amplification by angiotensin II type 1 receptor blockade using telmisartan. Am J Physiol Renal Physiol 296: F398–F405, 2009 - PubMed
    1. Anguiano L, Riera M, Pascual J, Valdivielso JM, Barrios C, Betriu A, Mojal S, Fernández E, Soler MJ; NEFRONA study: Circulating angiotensin-converting enzyme 2 activity in patients with chronic kidney disease without previous history of cardiovascular disease. Nephrol Dial Transplant 30: 1176–1185, 2015 - PMC - PubMed
    1. Zhou P, Yang XL, Wang XG, Hu B, Zhang L, Zhang W, Si HR, Zhu Y, Li B, Huang CL, Chen HD, Chen J, Luo Y, Guo H, Jiang RD, Liu MQ, Chen Y, Shen XR, Wang X, Zheng XS, Zhao K, Chen QJ, Deng F, Liu LL, Yan B, Zhan FX, Wang YY, Xiao GF, Shi ZL: A pneumonia outbreak associated with a new coronavirus of probable bat origin. Nature 579: 270–273, 2020 - PMC - PubMed
    1. Noordzij M, Duivenvoorden R, Pena MJ, de Vries H, Kieneker LM; Collaborative ERACODA Authors: ERACODA: The European database collecting clinical information of patients on kidney replacement therapy with COVID-19. Nephrol Dial Transplant 35: 2023–2025, 2020 - PMC - PubMed

Publication types

Substances