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Association of RASis and HMG-CoA reductase inhibitors with clinical manifestations in coronavirus disease 2019 patients: Results from the Khorshid Coronavirus Disease Cohort Study

Authors :
Bijan Iraj
Amir Reza Moravejolahkami
Ramin Sami
Maryam Riahinezhad
Zahra Tasdighi
Arash Toghyani
Nastaran Sadat Hosseini
Fatemeh Dehghan Niri
Gholamreza Askari
Source :
Journal of Research in Medical Sciences, Vol 28, Iss 1, Pp 15-15 (2023)
Publication Year :
2023
Publisher :
Wolters Kluwer Medknow Publications, 2023.

Abstract

Background: Angiotensin II receptor blockers (ARBs) and angiotensin-converting enzyme inhibitors (ACEinhs) may deteriorate or improve the clinical manifestations in severe acute respiratory syndrome coronavirus 2 infection. A comparative, cross-sectional study was conducted to evaluate the association of ARBs/ACEinhs and hydroxy-3-methyl-glutaryl-CoA reductase inhibitors (HMGRis) with clinical outcomes in coronavirus disease 2019 (COVID-19). Materials and Methods: From April 4 to June 2, 2020, 659 patients were categorized according to whether they were taking ARB, ACEinh, or HMGRi drugs or none of them. Demographic variables, clinical and laboratory tests, chest computed tomography findings, and intensive care unit-related data were analyzed and compared between the groups. Results: The ARB, ACEinh, and HMGRi groups significantly had lower heart rate (P < 0.05). Furthermore, a lower percent of O2 saturation (89.34 ± 7.17% vs. 84.25 ± 7.00%; P = 0.04) was observed in the ACEis group than non-ACEinhs. Mortality rate and the number of intubated patients were lower in patients taking ARBs, ACEinhs, and HMGRis, although these differences failed to reach statistical significance. Conclusion: Our findings present clinical data on the association between ARBs, ACEinhs, and HMGRis and outcomes in hospitalized, hypertensive COVID-19 patients, implying that ARBs/ACEinhs are not associated with the severity or mortality of COVID-19 in such patients.

Details

Language :
English
ISSN :
17351995 and 17357136
Volume :
28
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Journal of Research in Medical Sciences
Publication Type :
Academic Journal
Accession number :
edsdoj.f31b84bb50824ccbad090f8082e714f0
Document Type :
article
Full Text :
https://doi.org/10.4103/jrms.jrms_373_22