Antecedent Administration of Angiotensin-Converting Enzyme Inhibitors or Angiotensin II Receptor Antagonists and Survival After Hospitalization for COVID-19 Syndrome

被引:28
作者
Palazzuoli, Alberto [1 ,8 ]
Mancone, Massimo [2 ]
De Ferrari, Gaetano M. [3 ]
Forleo, Giovanni [4 ]
Secco, Gioel G. [5 ]
Ruocco, Gaetano M. [6 ]
D'Ascenzo, Fabrizio [3 ]
Monticone, Silvia [7 ]
Paggi, Anita [8 ]
Vicenzi, Marco [9 ]
Palazzo, Anna G. [10 ]
Landolina, Maurizio [11 ]
Taravelli, Erika [11 ]
Tavazzi, Guido [12 ]
Blasi, Francesco [13 ,14 ]
Infusino, Fabio [2 ]
Fedele, Francesco [2 ]
De Rosa, Francesco G. [10 ]
Emmett, Michael [15 ]
Schussler, Jeffrey M. [15 ,16 ,17 ]
Tecson, Kristen M. [15 ,16 ,17 ]
McCullough, Peter A. [15 ,16 ,17 ]
机构
[1] Univ Siena, AOUS Le Scotte Hosp, Dept Med Sci, Cardiovasc Dis Unit, Siena, Italy
[2] Sapienza Univ Rome, Dept Clin Internal Anesthesiol & Cardiovasc Sci, Rome, Italy
[3] Univ Turin, Citta Salute & Sci Le Molinette Hosp Torino, Dept Med Sci, Cardiol, Turin, Italy
[4] Pacing Azienda Osped Polo Univ Luigi Sacco, Sect Head Electrophysiol & Cardiac, Milan, Italy
[5] Azienda Osped SS Antonio & Biagio & Cesare Arrigo, Intervent Cardiol & Cardiac Surg Unit, Alessandria, Italy
[6] Regina Montis Regalis Hosp Mondovi, Div Cardiol, Cuneo, Italy
[7] Univ Turin, Dept Med Sci, Div Internal Med, Turin, Italy
[8] ASSST Nord Milano E Bassini Hosp Cisanello Balsam, Dept Internal Med, Intervent Cardiol, Milan, Italy
[9] Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Dept Internal Med, Cardiovasc Dis Unit, Milan, Italy
[10] Univ Torino, AOU Citta Salute & Sci, Dept Med Sci, Infect Dis, Turin, Italy
[11] Osped Maggiore Crema, Div Cardiol, Crema, Italy
[12] Univ Pavia, Fdn IRCCS Policlin San Matteo, Intens Care, Pavia, Italy
[13] Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policli, Resp Unit, Milan, Italy
[14] Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policli, Adult Cyst Fibrosis Ctr, Dept Internal Med, Milan, Italy
[15] Baylor Univ, Med Ctr, Dallas, TX USA
[16] Baylor Scott & White Heart & Vasc Hosp, Dallas, TX USA
[17] Baylor Heart & Vasc Inst, Dallas, TX USA
来源
JOURNAL OF THE AMERICAN HEART ASSOCIATION | 2020年 / 9卷 / 22期
关键词
angiotensin-converting enzyme inhibitor; angiotensin-converting enzyme-2; COVID-19; hospitalization; mortality; renin-angiotensin converting enzyme inhibitor; SARS-CoV-2; LUNG; DISEASE;
D O I
10.1161/JAHA.120.017364
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) utilizes the angiotensin-converting enzyme-2 (ACE-2) receptor to enter human cells. Angiotensin-converting enzyme inhibitors (ACEI) and angiotensin II receptor antagonists (ARB) are associated with ACE-2 upregulation. We hypothesized that antecedent use of ACEI/ARB may be associated with mortality in coronavirus disease 2019 (COVID-19). Methods and Results We used the Coracle registry, which contains data of patients hospitalized with COVID-19 in 4 regions of Italy, and restricted analyses to those >= 50 years of age. The primary outcome was in-hospital mortality. Among these 781 patients, 133 (17.0%) used an ARB and 171 (21.9%) used an ACEI. While neither sex nor smoking status differed by user groups, patients on ACEI/ARB were older and more likely to have hypertension, diabetes mellitus, and congestive heart failure. The overall mortality rate was 15.1% (118/781) and increased with age (P-Trend<0.0001). The crude odds ratios (ORs) for death for ACEI users and ARB users were 0.98, 95% CI, 0.60-1.60, P=0.9333, and 1.13, 95% CI, 0.67-1.91, P=0.6385, respectively. After adjusting for age, hypertension, diabetes mellitus, and congestive heart failure, antecedent ACEI administration was associated with reduced mortality (OR, 0.55; 95% CI, 0.31-0.98, P=0.0436); a similar, but weaker trend was observed for ARB administration (OR, 0.58; 95% CI, 0.32-1.07, P=0.0796). Conclusions In those aged >= 50 years hospitalized with COVID-19, antecedent use of ACEI was independently associated with reduced risk of inpatient death. Our findings suggest a protective role of renin-angiotensin-aldosterone system inhibition in patients with high cardiovascular risk affected by COVID-19.
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