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dc.contributor.authorCapraz, Mustafa
dc.contributor.authorTekcan, Akin
dc.contributor.authorCihangiroglu, Mustafa
dc.contributor.authorNursal, Ayse Feyda
dc.contributor.authorCapraz, Aylin
dc.contributor.authorMenekse, Elif
dc.contributor.authorDemir, Hatice Dortok
dc.date.accessioned2025-03-28T07:23:01Z
dc.date.available2025-03-28T07:23:01Z
dc.date.issued2025
dc.identifier.issn1525-7770
dc.identifier.issn1532-2335
dc.identifier.urihttps://doi.org/10.1080/15257770.2024.2395872
dc.identifier.urihttps://hdl.handle.net/20.500.12450/5986
dc.description.abstractThe coronavirus disease 2019 (COVID-19) is a recent pandemic occurring worldwide due to the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus, spreading mainly through large respiratory droplets or maybe through other transmission routes. The human genome has the most varied immune response genes correlated with infectious diseases. Genetic variants of mannose-binding lectin 2 (MBL2), an immunomodulatory gene, were associated with the risk, severity, and frequency of viral infections. In the present study, we hypothesized that the MBL2 gene rs1800450 variant could be associated with the development of COVID-19 disease in a Turkish population. Ninety-eight COVID-19 patients and 98 healthy, ethnically matched controls were studied. We isolated genomic DNA from whole blood and analyzed the MBL2 rs1800450 using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Associations were analyzed with the SPSS 20 statistical software. We found that MBL2 rs1800450 genotype distribution was significantly different between patients and controls. The patients had a higher MBL2 rs1800450 AA genotype than the controls had (4.94% in patients vs. 3.12% in controls, p=0.006). The subjects carrying AA genotype had a 10.83-fold increased risk for COVID-19 disease (OR = 10.83, %95CI = 1.359-86.349). We could not detect any significant difference between the COVID-19 patients and healthy controls in allele frequencies. Our findings demonstrated that the MBL2 rs1800450 BB genotype might increase the susceptibility to COVID-19 disease in the Turkish population. We suggest further studies with a larger sample size and other ethnic populations. HIGHLIGHTSComplement activation is involved in the pathogenesis of cardiovascular diseases through pleiotropic effects on inflammatory processes, endothelial and hematopoetic cell function, and hemostasis.MBL is a serum protein dependent on calcium that is effective in the innate immune response and binds to carbohydrates on the surface of several pathogens, activating the complement system or serving directly as an opsonin.It was found that COVID-19 patients had a higher MBL2 gene rs1800450 AA genotype than the controls.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Incen_US
dc.relation.ispartofNucleosides Nucleotides & Nucleic Acidsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCovid-19en_US
dc.subjectMBL2 geneen_US
dc.subjectvarianten_US
dc.titleThe effect of the MBL2 gene rs1800450 variant on COVID-19 development in Turkish patientsen_US
dc.typearticleen_US
dc.departmentAmasya Üniversitesien_US
dc.authoridKURUCA, Nilufer/0000-0001-5601-4952
dc.identifier.volume44en_US
dc.identifier.issue1en_US
dc.identifier.startpage79en_US
dc.identifier.endpage89en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-85203282516en_US
dc.identifier.doi10.1080/15257770.2024.2395872
dc.department-temp[Capraz, Mustafa] Amasya Univ, Dept Internal Med, Fac Med, Amasya, Turkiye; [Tekcan, Akin] Amasya Univ, Dept Med Biol, Fac Med, Amasya, Turkiye; [Cihangiroglu, Mustafa] Amasya Univ, Dept Infect Dis, Fac Med, Amasya, Turkiye; [Nursal, Ayse Feyda] Hitit Univ, Dept Med Genet, Fac Med, Corum, Turkiye; [Capraz, Aylin] Amasya Univ, Dept Chest Dis, Fac Med, Amasya, Turkiye; [Menekse, Elif] Amasya Univ, Lab Med Biochem, Sabuncuoglu Serefeddin Educ & Res Hosp, Amasya, Turkiye; [Demir, Hatice Dortok] Amasya Univ, Dept Med Biochem, Fac Med, Amasya, Turkiye; [Kuruca, Nilufer] Ondokuz Mayis Univ, Dept Pathol, Fac Vet Med, Samsun, Turkiye; [Yigit, Serbulent] Ondokuz Mays Univ, Dept Genet, Fac Vet Med, Samsun, Turkiyeen_US
dc.identifier.wosWOS:001308466400001en_US
dc.identifier.pmid39210720en_US
dc.snmzKA_WOS_20250328
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US


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