Host Genetic Polymorphisms and Disease Severity in Pregnant Women with COVID-19 in Türkiye
Özet
Objective: The study aimed to analyze the association between coronavirus disease-2019 (COVID-19) disease severity and genetic susceptibility in pregnant women. Material and Methods: The research included 54 pregnant women with confirmed COVID-19 diagnosis. All volunteers were evaluated physically and biochemically. Angiotensin-converting enzyme (ACE)2 (p.T27A A>G, p.G326E G>A, p.K419T A>C, ACE (p.T776T A>G, and g.16471_16472delinsALU (I/D), AGTR1 c.*86A>C, methylenetetrahydrofolate-reductase (MTHFR) p.A222V C>T and PAI-1-844 G>A were analyzed. Results: The allele frequency was also compared with control groups of the different studies made on Turkish women. MTHFR “CT” genotype compared to “CC” had lower platelet counts (p=0.015). In ACE “ID” genotype, there was a lower D-dimer level compared to “DD” genotype (p=0.02). In PAI-1-844G>A, the AA vs. AG+GG genotype and AA vs. GG genotype elevate the risk of hospitalization 6.4-fold (OR: 6.4 95% (Cl): 1.6-25.8 p=0.009), and 4.6-fold (OR: 4.6 95% CI:1.0-21.6 p=0.049), respectively. In MTHFR p.A222V, to have CC vs. CT genotype increased the risk of enoxaparin and antibiotic use 4.1-fold and 3.2-fold at the borderline significance (OR: 4.1 95% Cl: 0.99-16.9 p=0.052 and OR: 3.2 95% Cl: 0.98-10.5 p=0.053), respectively. An allele frequency difference wasn't found between the patient and the healthy women related to the investigated polymorphisms. Conclusion: PAI-1-844G>A, MTHFR p.A222V, and ACE (I/D) associated with a poor COVID-19 outcome, the risk of enoxaparin and antibiotic use, and also increased risk of hospitalization. Allele frequencies of the genes were not different between healthy control women and women with COVID-19; genetic variation may not influence the risk of infection but disease severity. Copyright © 2024 by Türkiye Klinikleri.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Polat, Seher | |
| dc.contributor.author | Kiremitli, Sevil | |
| dc.contributor.author | Kiremitli, Tunay | |
| dc.contributor.author | Kirkinci, Ahmet | |
| dc.contributor.author | Kurnuç, Fatma Zehra | |
| dc.contributor.author | Arslan, Yusuf Kemal | |
| dc.date.accessioned | 2026-10-18T20:26:55.665312624Z | |
| dc.date.available | 2026-10-18T20:26:55.665312624Z | |
| dc.date.issued | 2024 | |
| dc.description.abstract | Objective: The study aimed to analyze the association between coronavirus disease-2019 (COVID-19) disease severity and genetic susceptibility in pregnant women. Material and Methods: The research included 54 pregnant women with confirmed COVID-19 diagnosis. All volunteers were evaluated physically and biochemically. Angiotensin-converting enzyme (ACE)2 (p.T27A A>G, p.G326E G>A, p.K419T A>C, ACE (p.T776T A>G, and g.16471_16472delinsALU (I/D), AGTR1 c.*86A>C, methylenetetrahydrofolate-reductase (MTHFR) p.A222V C>T and PAI-1-844 G>A were analyzed. Results: The allele frequency was also compared with control groups of the different studies made on Turkish women. MTHFR “CT” genotype compared to “CC” had lower platelet counts (p=0.015). In ACE “ID” genotype, there was a lower D-dimer level compared to “DD” genotype (p=0.02). In PAI-1-844G>A, the AA vs. AG+GG genotype and AA vs. GG genotype elevate the risk of hospitalization 6.4-fold (OR: 6.4 95% (Cl): 1.6-25.8 p=0.009), and 4.6-fold (OR: 4.6 95% CI:1.0-21.6 p=0.049), respectively. In MTHFR p.A222V, to have CC vs. CT genotype increased the risk of enoxaparin and antibiotic use 4.1-fold and 3.2-fold at the borderline significance (OR: 4.1 95% Cl: 0.99-16.9 p=0.052 and OR: 3.2 95% Cl: 0.98-10.5 p=0.053), respectively. An allele frequency difference wasn't found between the patient and the healthy women related to the investigated polymorphisms. Conclusion: PAI-1-844G>A, MTHFR p.A222V, and ACE (I/D) associated with a poor COVID-19 outcome, the risk of enoxaparin and antibiotic use, and also increased risk of hospitalization. Allele frequencies of the genes were not different between healthy control women and women with COVID-19; genetic variation may not influence the risk of infection but disease severity. Copyright © 2024 by Türkiye Klinikleri. | |
| dc.identifier.doi | 10.5336/jcog.2023-96185 | |
| dc.identifier.eissn | 2619-9467 | |
| dc.identifier.endpage | 9 | |
| dc.identifier.issn | 2619-9467 | |
| dc.identifier.issue | 1 | |
| dc.identifier.scopus | 2-s2.0-85190966878 | |
| dc.identifier.startpage | 1 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/11953 | |
| dc.identifier.volume | 34 | |
| dc.identifier.wos | WOS:001212008000001 | |
| dc.language.iso | en | |
| dc.publisher | OrtadogÂu Reklam Tanitim Yayincilik Turizm Egitim Insaat Sanayi ve Ticaret A.S. | |
| dc.relation.ispartof | Journal of Clinical Obstetrics and Gynecology | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | COVID-19 | |
| dc.subject | gene polymorphism | |
| dc.subject | genetic susceptibility | |
| dc.subject | pregnant women | |
| dc.subject | 5,10 methylenetetrahydrofolate reductase (FADH2) | |
| dc.subject | angiotensin converting enzyme 2 | |
| dc.subject | antibiotic agent | |
| dc.subject | enoxaparin | |
| dc.subject | plasminogen activator inhibitor 1 | |
| dc.subject | adult | |
| dc.subject | Article | |
| dc.subject | biochemical analysis | |
| dc.subject | cohort analysis | |
| dc.subject | controlled study | |
| dc.subject | coronavirus disease 2019 | |
| dc.subject | disease severity | |
| dc.subject | DNA polymorphism | |
| dc.subject | female | |
| dc.subject | gene frequency | |
| dc.subject | genotype | |
| dc.subject | hospitalization | |
| dc.subject | human | |
| dc.subject | human cell | |
| dc.subject | major clinical study | |
| dc.subject | pregnant woman | |
| dc.subject | risk assessment | |
| dc.subject | Turkey (republic) | |
| dc.title | Host Genetic Polymorphisms and Disease Severity in Pregnant Women with COVID-19 in Türkiye | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 0 | |
| rdl.citation.trdizin | 0 | |
| rdl.citation.wos | 0 | |
| rdl.department | ÇUKUROVA ÜNİVERSİTESİ | |
| rdl.department | ERZİNCAN BİNALİ YILDIRIM ÜNİVERSİTESİ | |
| rdl.oa.status | open | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | TRDIZIN | |
| rdl.wos.index | Emerging Sources Citation Index (ESCI) |
