TY - JOUR
T1 - RAAS inhibitors are not associated with mortality in COVID-19 patients
T2 - Findings from an observational multicenter study in Italy and a meta-analysis of 19 studies
AU - The COvid-19 RISk and Treatments (CORIST) collaboration
AU - Di Castelnuovo, Augusto
AU - Costanzo, Simona
AU - Antinori, Andrea
AU - Berselli, Nausicaa
AU - Blandi, Lorenzo
AU - Bonaccio, Marialaura
AU - Cauda, Roberto
AU - Gialluisi, Alessandro
AU - Guaraldi, Giovanni
AU - Menicanti, Lorenzo
AU - Mennuni, Marco
AU - Mussinelli, Roberta
AU - My, Ilaria
AU - Parruti, Giustino
AU - Patti, Giuseppe
AU - Perlini, Stefano
AU - Santilli, Francesca
AU - Signorelli, Carlo
AU - Stefanini, Giulio G.
AU - Vergori, Alessandra
AU - Abete, Pasquale
AU - Ageno, Walter
AU - Agostoni, Piergiuseppe
AU - Aiello, Luca
AU - Al Moghazi, Samir
AU - Arboretti, Rosa
AU - Aucella, Filippo
AU - Barbieri, Greta
AU - Barchitta, Martina
AU - Bartoloni, Alessandro
AU - Bonfanti, Paolo
AU - Cacciatore, Francesco
AU - Caiano, Lucia
AU - Carrozzi, Laura
AU - Cascio, Antonio
AU - Castiglione, Giacomo
AU - Cianfrone, Stefania
AU - Ciccullo, Arturo
AU - Cingolani, Antonella
AU - Cipollone, Francesco
AU - Colomba, Claudia
AU - Colombo, Crizia
AU - Cozzi, Ottavia
AU - Crisetti, Annalisa
AU - Crosta, Francesca
AU - Danzi, Gian Battista
AU - D'Ardes, Damiano
AU - de Gaetano Donati, Katleen
AU - Di Gennaro, Francesco
AU - Di Tano, Giuseppe
N1 - Publisher Copyright:
© 2020 Elsevier Inc.
PY - 2020/12
Y1 - 2020/12
N2 - Objective: The hypothesis that been set forward that use of Renin Angiotensin Aldosterone System (RAAS) inhibitors is associated with COVID−19 severity. We set-up a multicenter Italian collaboration (CORIST Project, ClinicalTrials.gov ID: NCT04318418) to retrospectively investigate the relationship between RAAS inhibitors and COVID−19 in-hospital mortality. We also carried out an updated meta-analysis on the relevant studies. Methods: We analyzed 4069 unselected patients with laboratory-confirmed SARS-CoV-2 infection and hospitalized in 34 clinical centers in Italy from February 19, 2020 to May 23, 2020. The primary end-point in a time-to event analysis was in-hospital death, comparing patients who received angiotensin-converting–enzyme inhibitors (ACE[sbnd]I) or angiotensin-receptor blockers (ARB) with patients who did not. Articles for the meta-analysis were retrieved until July 13th, 2020 by searching in web-based libraries, and data were combined using the general variance-based method. Results: Out of 4069 COVID−19 patients, 13.5% and 13.3% received ACE-I or ARB, respectively. Use of neither ACE-I nor ARB was associated with mortality (multivariable hazard ratio (HR) adjusted also for COVID−19 treatments: 0.96, 95% confidence interval 0.77–1.20 and HR = 0.89, 0.67–1.19 for ACE-I and ARB, respectively). Findings were similar restricting the analysis to hypertensive (N = 2057) patients (HR = 1.00, 0.78–1.26 and HR = 0.88, 0.65–1.20) or when ACE-I or ARB were considered as a single group. Results from the meta-analysis (19 studies, 29,057 COVID−19 adult patients, 9700 with hypertension) confirmed the absence of association. Conclusions: In this observational study and meta-analysis of the literature, ACE-I or ARB use was not associated with severity or in-hospital mortality in COVID−19 patients.
AB - Objective: The hypothesis that been set forward that use of Renin Angiotensin Aldosterone System (RAAS) inhibitors is associated with COVID−19 severity. We set-up a multicenter Italian collaboration (CORIST Project, ClinicalTrials.gov ID: NCT04318418) to retrospectively investigate the relationship between RAAS inhibitors and COVID−19 in-hospital mortality. We also carried out an updated meta-analysis on the relevant studies. Methods: We analyzed 4069 unselected patients with laboratory-confirmed SARS-CoV-2 infection and hospitalized in 34 clinical centers in Italy from February 19, 2020 to May 23, 2020. The primary end-point in a time-to event analysis was in-hospital death, comparing patients who received angiotensin-converting–enzyme inhibitors (ACE[sbnd]I) or angiotensin-receptor blockers (ARB) with patients who did not. Articles for the meta-analysis were retrieved until July 13th, 2020 by searching in web-based libraries, and data were combined using the general variance-based method. Results: Out of 4069 COVID−19 patients, 13.5% and 13.3% received ACE-I or ARB, respectively. Use of neither ACE-I nor ARB was associated with mortality (multivariable hazard ratio (HR) adjusted also for COVID−19 treatments: 0.96, 95% confidence interval 0.77–1.20 and HR = 0.89, 0.67–1.19 for ACE-I and ARB, respectively). Findings were similar restricting the analysis to hypertensive (N = 2057) patients (HR = 1.00, 0.78–1.26 and HR = 0.88, 0.65–1.20) or when ACE-I or ARB were considered as a single group. Results from the meta-analysis (19 studies, 29,057 COVID−19 adult patients, 9700 with hypertension) confirmed the absence of association. Conclusions: In this observational study and meta-analysis of the literature, ACE-I or ARB use was not associated with severity or in-hospital mortality in COVID−19 patients.
KW - ACE-I
KW - ARB
KW - Angiotensin converting enzyme inhibitors
KW - Angiotensin receptor blockers
KW - COVID−19
KW - Mortality
KW - Sartans
UR - https://www.scopus.com/pages/publications/85093963915
U2 - 10.1016/j.vph.2020.106805
DO - 10.1016/j.vph.2020.106805
M3 - Article
SN - 1537-1891
VL - 135
JO - Vascular Pharmacology
JF - Vascular Pharmacology
M1 - 106805
ER -