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 (ACEeI) 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.

RAAS inhibitors are not associated with mortality in COVID-19 patients: Findings from an observational multicenter study in Italy and a meta-analysis of 19 studies

Barbieri, G;Carrozzi, L;Mengozzi, A;Menichetti, F;Minutolo, F;De Caterina, R;
2020-01-01

Abstract

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 (ACEeI) 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.
2020
Di Castelnuovo, A; Costanzo, S; Antinori, A; Berselli, N; Blandi, L; Bonaccio, M; Cauda, R; Gialluisi, A; Guaraldi, G; Menicanti, L; Mennuni, M; Mussinelli, R; My, I; Parruti, G; Patti, G; Perlini, S; Santilli, F; Signorelli, C; Stefanini, Gg; Vergori, A; Abete, P; Ageno, W; Agostoni, P; Aiello, L; Moghazi, Sa; Arboretti, R; Aucella, F; Barbieri, G; Barchitta, M; Bartoloni, A; Bonfanti, P; Cacciatore, F; Caiano, L; Carrozzi, L; Cascio, A; Castiglione, G; Cianfrone, S; Ciccullo, A; Cingolani, A; Cipollone, F; Colomba, C; Colombo, C; Cozzi, O; Crisetti, A; Crosta, F; Danzi, Gb; D'Ardes, D; Donati, Kd; Di Gennaro, F; Di Tano, G; D'Offizi, G; Fusco, Fm; Gentile, I; Graziani, E; Guarnieri, G; Larizza, G; Leone, A; Lio, V; Lucia, Mb; Maccagni, G; Madaro, F; Maitan, S; Mancarella, S; Manuele, R; Mapelli, M; Maragna, R; Marcucci, R; Maresca, G; Marongiu, S; Marotta, C; Marra, L; Mastroianni, F; Mazzitelli, M; Mengozzi, A; Menichetti, F; Meschiari, M; Milic, J; Minutolo, F; Molena, B; Mussini, C; Musso, M; Odone, A; Olivieri, M; Palimodde, A; Pasi, E; Pesavento, R; Petri, F; Pinchera, B; Pivato, Ca; Poletti, V; Ravaglia, C; Rossato, M; Rossi, M; Sabena, A; Salinaro, F; Sangiovanni, V; Sanrocco, C; Scoppettuolo, G; Scorzolini, L; Sgariglia, R; Simeone, Pg; Trecarichi, Em; Vettor, R; Vianello, A; Vinceti, M; Virano, A; Vocciante, L; De Caterina, R; Iacoviello, L
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/1066605
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