Risks of ACE Inhibitor and ARB Usage in COVID-19: Evaluating the Evidence

被引:108
作者
Sriram, Krishna [1 ]
Insel, Paul A. [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
关键词
ANGIOTENSIN-CONVERTING ENZYME; SYSTEM BLOCKADE; EXPRESSION; KIDNEY; PHARMACOKINETICS; RECEPTOR; ENALAPRIL; LOSARTAN; PLASMA; RATS;
D O I
10.1002/cpt.1863
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Concerns have been raised regarding the safety of angiotensin converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) in patients with coronavirus disease of 2019 (COVID-19), based on the hypothesis that such medications may raise expression of ACE2, the receptor for severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2). We conducted a literature review of studies (n = 12) in experimental animals and human subjects (n = 12) and evaluated the evidence regarding the impact of administration of ACEIs and ARBs on ACE2 expression. We prioritized studies that assessed ACE2 protein expression data, measured directly or inferred from ACE2 activity assays. The findings in animals are inconsistent with respect to an increase in ACE2 expression in response to treatment with ACEIs or ARBs. Control/sham animals show little to no effect in the plurality of studies. Those studies that report increases in ACE2 expression tend to involve acute injury models and/or higher doses of ACEIs or ARBs than are typically administered to patients. Data from human studies overwhelmingly imply that administration of ACEIs/ARBs does not increase ACE2 expression. Available evidence, in particular, data from human studies, does not support the hypothesis that ACEI/ARB use increases ACE2 expression and the risk of complications from COVID-19. We conclude that patients being treated with ACEIs and ARBs should continue their use for approved indications.
引用
收藏
页码:236 / 241
页数:6
相关论文
共 53 条
[1]   Circulating angiotensin-converting enzyme 2 activity in patients with chronic kidney disease without previous history of cardiovascular disease [J].
Anguiano, Lidia ;
Riera, Marta ;
Pascual, Julio ;
Manuel Valdivielso, Jose ;
Barrios, Clara ;
Betriu, Angels ;
Mojal, Sergi ;
Fernandez, Elvira ;
Jose Soler, Maria .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2015, 30 (07) :1176-1185
[2]  
Bi BT, 2012, EUR REV MED PHARMACO, V16, P2162
[3]  
Bozkurt B, 2020, HFSA ACC AHA STATEME
[4]   Combination renin-angiotensin system blockade and angiotensin-converting enzyme 2 in experimental myocardial infarction: implications for future therapeutic directions [J].
Burchill, Luke J. ;
Velkoska, Elena ;
Dean, Rachael G. ;
Griggs, Karen ;
Patel, Sheila K. ;
Burrell, Louise M. .
CLINICAL SCIENCE, 2012, 123 (11-12) :649-658
[5]   Chronic kidney disease: cardiac and renal angiotensin-converting enzyme (ACE) 2 expression in rats after subtotal nephrectomy and the effect of ACE inhibition [J].
Burrell, L. M. ;
Burchill, L. ;
Dean, R. G. ;
Griggs, K. ;
Patel, S. K. ;
Velkoska, E. .
EXPERIMENTAL PHYSIOLOGY, 2012, 97 (04) :477-485
[6]   Renin-Angiotensin System Blockers and the COVID-19 Pandemic At Present There Is No Evidence to Abandon Renin-Angiotensin System Blockers [J].
Danser, A. H. Jan ;
Epstein, Murray ;
Batlle, Daniel .
HYPERTENSION, 2020, 75 (06) :1382-1385
[7]  
Dubey Ramkumar, 2015, Sci Pharm, V83, P107, DOI 10.3797/scipharm.1410-15
[8]   Detection of soluble angiotensin-converting enzyme 2 in heart failure [J].
Epelman, Slava ;
Tang, W. H. Wilson ;
Chen, Stephen Y. ;
Van Lente, Frederick ;
Francis, Gary S. ;
Sen, Subha .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2008, 52 (09) :750-754
[9]   Are patients with hypertension and diabetes mellitus at increased risk for COVID-19 infection? [J].
Fang, Lei ;
Karakiulakis, George ;
Roth, Michael .
LANCET RESPIRATORY MEDICINE, 2020, 8 (04) :E21-E21
[10]   Effects of renin-angiotensin system blockade on renal angiotensin-(1-7) forming enzymes and receptors [J].
Ferrario, CM ;
Jessup, J ;
Gallagher, PE ;
Averill, DB ;
Brosnihan, KB ;
Tallant, EA ;
Smith, RD ;
Chappell, MC .
KIDNEY INTERNATIONAL, 2005, 68 (05) :2189-2196