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The Association Between Genetic Variants in ACE1and ACE2 Genes with Susceptibility to COVID-19 Infection.
- Source :
-
Biochemical genetics [Biochem Genet] 2024 Dec; Vol. 62 (6), pp. 4679-4692. Date of Electronic Publication: 2024 Feb 13. - Publication Year :
- 2024
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Abstract
- Angiotensin-converting enzyme 2 (ACE2) receptors facilitate the entry of the causative virus severe acute respiratory syndrome coronavirus 2 (SARS‑CoV‑2) into target cells. Some ACE gene variants have been suggested to be involved in COVID-19 pathogenesis. So, the aim was to assess the association between ACE1 rs4646994 and ACE2 rs2285666 genes polymorphisms and the susceptibility and severity of COVID-19. This case-control study was conducted on 197 patients with COVID-19 and 197 healthy controls. ACE-1 insertion/deletion (I/D) (rs4646994) and ACE2 rs2285666 genes polymorphisms were determined by the amplification refractory mutation system- polymerase chain reaction (ARMS-PCR) technique. The DD genotype of ACE1 I/D polymorphism was associated with increased susceptibility to COVID-19 infection (p = 0.012), whereas the ID genotype of this polymorphism was associated with decreased susceptibility (p = 0.003) (significance level = 0.017). There was no significant association in allele and genotype distribution of ACE2 rs2285666 polymorphism between cases and controls. The ACE1 I/D polymorphism may be considered as a risk factor for COVID-19 susceptibility.<br />Competing Interests: Declarations. Ethical Approval: The Ethics Committee of Birjand University of Medical Sciences, Birjand, Iran approved the study (Ethical code: IR.BUMS.REC.1399.060). Consent to Participate: A written informed consent was obtained from all participants in this study. Consent for Publication: Not applicable. Competing Interests: The authors declare no competing interests.<br /> (© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
Details
- Language :
- English
- ISSN :
- 1573-4927
- Volume :
- 62
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Biochemical genetics
- Publication Type :
- Academic Journal
- Accession number :
- 38349438
- Full Text :
- https://doi.org/10.1007/s10528-024-10722-8