Unknown

Dataset Information

0

Potential harmful effects of discontinuing ACE-inhibitors and ARBs in COVID-19 patients.


ABSTRACT: The discovery of angiotensin converting enzyme-2 (ACE-2) as the receptor for SARS- CoV-2 (Severe Acute Respiratory Syndrome Coronavirus-2) has implicated the renin-angiotensin-aldosterone system in acute respiratory distress syndrome (ARDS) and respiratory failure in patients with coronavirus disease-19 (COVID-19). The angiotensin converting enzyme-1-angiotensin II-angiotensin AT1 receptor pathway contributes to the pathophysiology of ARDS, whereas activation of the ACE-2-angiotensin(1-7)-angiotensin AT2 receptor and the ACE-2-angiotensin(1-7)-Mas receptor pathways have been shown to be protective. Here we propose and discuss therapeutic considerations how to increase soluble ACE-2 in plasma in order for ACE-2 to capture and thereby inactivate SARS-CoV-2. This could be achieved by administering recombinant soluble ACE-2. We also discuss why and how ACEIs and ARBs provide cardiovascular, renal and also pulmonary protection in SARS-CoV-2- associated ARDS. Discontinuing these medications in COVID-19 patients may therefore potentially be harmful.

SUBMITTER: Rossi GP 

PROVIDER: S-EPMC7198232 | biostudies-literature | 2020 Apr

REPOSITORIES: biostudies-literature

altmetric image

Publications

Potential harmful effects of discontinuing ACE-inhibitors and ARBs in COVID-19 patients.

Rossi Gian Paolo GP   Sanga Viola V   Barton Matthias M  

eLife 20200406


The discovery of angiotensin converting enzyme-2 (ACE-2) as the receptor for SARS- CoV-2 (Severe Acute Respiratory Syndrome Coronavirus-2) has implicated the renin-angiotensin-aldosterone system in acute respiratory distress syndrome (ARDS) and respiratory failure in patients with coronavirus disease-19 (COVID-19). The angiotensin converting enzyme-1-angiotensin II-angiotensin AT<sub>1</sub> receptor pathway contributes to the pathophysiology of ARDS, whereas activation of the ACE-2-angiotensin(  ...[more]

Similar Datasets

| S-EPMC7561344 | biostudies-literature
| S-EPMC7958102 | biostudies-literature
| S-EPMC7595232 | biostudies-literature
2023-07-26 | GSE227585 | GEO
| S-EPMC7753609 | biostudies-literature
| S-EPMC7502385 | biostudies-literature