Evidence map›Paper›PMID 41734172›Full record

ArticlePloS one2026

The synergistic interaction between ACE and TMPRSS2 polymorphisms increases the risk of severe COVID-19.

Odonchimeg Bayaraa, Chimedlkhamsuren Ganbold, Bayarlakh Byambadorj, Zolzaya Battulga, Ichinnorov Dashtseren, Sarantuya Jav

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Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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6 authors.

Odonchimeg BayaraaDepartment of Pulmonology and Allergy, School of Medicine, Mongolian National University of Medical Science, Ulaanbaatar, Mongolia.
Chimedlkhamsuren GanboldDepartment of Molecular Biology and Genetics, School of Biomedicine, Mongolian National University of Medical Science, Ulaanbaatar, Mongolia.
Bayarlakh ByambadorjDepartment of Molecular Biology and Genetics, School of Biomedicine, Mongolian National University of Medical Science, Ulaanbaatar, Mongolia.ORCID https://orcid.org/0000-0002-8164-681X
Zolzaya BattulgaDepartment of Molecular Biology and Genetics, School of Biomedicine, Mongolian National University of Medical Science, Ulaanbaatar, Mongolia.ORCID https://orcid.org/0000-0002-1467-1169
Ichinnorov DashtserenDepartment of Pulmonology and Allergy, School of Medicine, Mongolian National University of Medical Science, Ulaanbaatar, Mongolia.
Sarantuya JavDepartment of Molecular Biology and Genetics, School of Biomedicine, Mongolian National University of Medical Science, Ulaanbaatar, Mongolia.ORCID https://orcid.org/0000-0002-3032-4490

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Within a few years after the pandemic outbreak, several of evidence have found to suggest that the genetic factors influence the severity and mortality rate of COVID-19. In particular, the identification of genetic markers that increase the risk of severe or critical COVID-19 is important for public health management during the pandemic. By August 2021, 88.9% of Mongolian population had been vaccinated. Therefore, we conducted this study to compare the polymorphisms of candidate genes by selecting people who developed mild or severe COVID-19 within this vaccinated population. A total of 90 patients with severe COVID-19, 95 patients with mild COVID-19, and 90 asymptomatic patients were participated in present cross-sectional study. rs4646994, rs4240157, rs41423247, rs56149945, rs10052957, rs12329760, rs4303795, rs75603675 and rs17854725 polymorphisms of the ACE, ACE2, NR3C1 and TMPRSS2 genes were genotyped. Genotyping performed by real-time PCR, RFLP and allele-specific PCR methods. Odds ratio, 95% confidence interval, p value were calculated using logistic regression analysis. SNP-SNP interaction were explored using multi-dimensional reduction analysis. P values for multivariate model was corrected by Bonferroni correction. Totally 10 polymorphisms of above-mentioned genes were genotyped among the groups. Only A/C genotype frequencies of rs75603675 were significantly different between groups. Compared with mild COVID-19 group, the participants who carrying A/C genotype of rs75603675 had 3.58-fold (95% CI, 1.38-9.29, p = 0.009) higher risk for severe COVID-19. In addition, the synergistic interaction (RERI = 2.573; AP = 0.934; S = 8.352) was observed between D/D or I/D genotype of rs4646994 and A/C genotype of rs75603675, which combination (OR=4.88, 95% CI, 1.38-18.01, p = 0.014, Power = 91.1%) was associated with increased risk of severe COVID-19 after Bonferroni correction. Our result suggesting that the combination of rs4646994 of the ACE gene and rs75603675 of the TMPRSS2 gene is associated with increased risk of severe COVID-19.

Indexed as

COVID-19Peptidyl-Dipeptidase APolymorphism, Single NucleotideSerine EndopeptidasesAdultAgedCross-Sectional StudiesFemaleGenetic Predisposition to DiseaseGenotypeHumansMaleMiddle AgedMongoliaSARS-CoV-2Severity of Illness IndexACE protein, humanPeptidyl-Dipeptidase ASerine EndopeptidasesTMPRSS2 protein, human

Identifiers

PMID41734172
PMCPMC12931805

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