Is There an Association Between COVID-19 Mortality and the Renin-Angiotensin System? A Call for Epidemiologic Investigations. (26th March 2020)

• Record Type: Journal Article
• Authors: Hanff, Thomas C; Harhay, Michael O; Brown, Tyler S; Cohen, Jordana B; Mohareb, Amir M
• Is Part Of: Clinical infectious diseases. Volume 71:Number 15(2020)
• Page Start: 870
• Page End: 874
• Publication Date: 2020-03-26
• Subjects: COVID-19 -- SARS-CoV-2 -- angiotensin-converting enzyme 2 -- renin-angiotensin system -- cardiovascular disease; Communicable diseases -- Periodicals; 616.905
• DOI: 10.1093/cid/ciaa329
• Languages: English
• ISSNs: 1058-4838

Abstract

Abstract: Mortality from coronavirus disease 2019 (COVID-19) is strongly associated with cardiovascular disease, diabetes, and hypertension. These disorders share underlying pathophysiology related to the renin-angiotensin system (RAS) that may be clinically insightful. In particular, activity of the angiotensin-converting enzyme 2 (ACE2) is dysregulated in cardiovascular disease, and this enzyme is used by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) to initiate the infection. Cardiovascular disease and pharmacologic RAS inhibition both increase ACE2 levels, which may increase the virulence of SARS-CoV-2 within the lung and heart. Conversely, mechanistic evidence from related coronaviruses suggests that SARS-CoV-2 infection may downregulate ACE2, leading to toxic overaccumulation of angiotensin II that induces acute respiratory distress syndrome and fulminant myocarditis. RAS inhibition could mitigate this effect. With conflicting mechanistic evidence, we propose key clinical research priorities necessary to clarify the role of RAS inhibition in COVID-19 mortality that could be rapidly addressed by the international research community. Abstract : The association between coronavirus disease 2019 (COVID-19) mortality and cardiovascular disease is likely mediated by dysregulation of the renin-angiotensin system (RAS). Pharmacoepidemiologic studies are needed to clarify whether RAS inhibition mediates this association and is helpful or harmful.