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Are COVID-19 Polymorphisms in ACE and ACE2 Prognosis Predictors?

Authors :
Guarienti FA
Xavier FAC
Ferraz MD
Wagner F
Marinowic DR
da Costa JC
Machado DC
Source :
Current issues in molecular biology [Curr Issues Mol Biol] 2024 Jul 28; Vol. 46 (8), pp. 8111-8117. Date of Electronic Publication: 2024 Jul 28.
Publication Year :
2024

Abstract

Regardless of the containment of the SARS-CoV-2 pandemic, it remains paramount to comprehensively understand its underlying mechanisms to mitigate potential future health and economic impacts, comparable to those experienced throughout the course of the pandemic. The angiotensin-converting enzyme 2 (ACE2) provides anchorage for SARS-CoV-2 binding, thus implicating that ACE and ACE2 might contribute to the variability in infection severity. This study aimed to elucidate predisposing factors influencing the disease course among people infected by SARS-CoV-2, focusing on angiotensin-converting enzyme (ACE) and ACE2 polymorphisms. Notably, despite similar demographics and comorbidities, COVID-19 patients exhibit substantial differences in prognosis. Genetic polymorphisms in ACE and ACE2 have been implicated in disease progression, prompting our investigation into their role in COVID-19 evolution. Using next-generation sequencing (NGS), we analyzed ACE and ACE2 genes in a sample group comprising six subjects infected by SARS-CoV-2. Our findings revealed a correlation between specific polymorphisms and COVID-19 outcomes. Specifically, ACE and ACE2 intronic deletions were observed in all deceased patients, suggesting a potential association with mortality. These results highlight the significance of genetic factors in shaping the clinical course of COVID-19, emphasizing the importance of further research into the impact of genetic variations on COVID-19 severity.

Details

Language :
English
ISSN :
1467-3045
Volume :
46
Issue :
8
Database :
MEDLINE
Journal :
Current issues in molecular biology
Publication Type :
Academic Journal
Accession number :
39194697
Full Text :
https://doi.org/10.3390/cimb46080480