Correlation of ITGB3 Gene rs5918T>C and APOA1 Gene rs1799837C>T Variants with Serum Lipid Profiles in Turkish Cypriot Patients with Coronary Artery Disease

dc.contributor.authorConkbayir, Cenk
dc.contributor.authorErgoren, Mahmut Cerkez
dc.contributor.authorCobanogullari, Havva
dc.contributor.authorBalcioglu, Ozlem
dc.contributor.authorAbras, Irem
dc.contributor.authorEminsel, Tengul
dc.contributor.authorTemel, Sehime Gulsun
dc.date.accessioned2026-02-06T18:23:52Z
dc.date.issued2025
dc.departmentDoğu Akdeniz Üniversitesi
dc.description.abstractAim: The relationship between hypercholesterolemia, particularly elevated low density lipoprotein-cholesterol (LDL-C) levels and coronary artery disease is recognized by the evidence from previous epidemiologic studies. Importantly, genetic polymorphisms on different genes have been reported to be associated with plasma lipid levels. In this particular study, we aimed to investigate the relationship between the ITGB3 gene rs5918 T>C and APO-A1 gene rs1799837 C>T markers and serum lipid metabolism. Patients and methods: A total of 100 subjects with CAD and 250 healthy subjects were involved in the current study. A basic biochemical analysis, including serum glucose, total serum cholesterol, HDL-C, LDL-C and triglycerides, was performed for each participant. Genotyping for the ITG83 gene and APO-A1 gene polymorphisms was performed by polymerase chain reaction followed by restriction fragment length polymorphism (RFLP) analysis. Results: With respect to the genotype and allele distributions of ITG83 rs5918 T>C polymorphism, the frequency of the C allele was higher in the coronary artery disease (CAD) group compared to the control group (p = 0.001). Moreover, there was a statistically significant association detected between ITG83 rs5918 CC genotype and serum total cholesterol (TC) and high-density lipoprotein cholesterol (HDL-C) (p = 0.0006, p = 0.016, respectively) in CAD group. However there was no statistically significant association was identified between the APOA1 rs1799837 C>T polymorphism and biochemical parameters in control and CAD group. Conclusion: The results demonstrated that rs5918 T>C variant within the ITG83 gene might have a clinical importance as a genetic marker which increases the susceptibility to CAD. Therefore, the ITG83 gene rs5918 C allele may be offered as a screening option for CAD in Turkish Cypriot population who come in for medical check-up.
dc.identifier.doi10.33678/cor.2025.004
dc.identifier.endpage366
dc.identifier.issn0010-8650
dc.identifier.issn1803-7712
dc.identifier.issue3
dc.identifier.orcid0000-0003-4153-7739
dc.identifier.scopus2-s2.0-105010044597
dc.identifier.scopusqualityQ4
dc.identifier.startpage360
dc.identifier.urihttps://doi.org/10.33678/cor.2025.004
dc.identifier.urihttps://hdl.handle.net/11129/9945
dc.identifier.volume67
dc.identifier.wosWOS:001524062600006
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherCzech Soc Cardiology & Czech Soc Cardiovascular Surgery
dc.relation.ispartofCor Et Vasa
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260204
dc.subjectAPO-A1
dc.subjectCoronary artery disease
dc.subjectHDL-C
dc.subjectITGB3
dc.subjectLDL-C
dc.subjectPolymorphism
dc.subjectTurkish Cypriot
dc.titleCorrelation of ITGB3 Gene rs5918T>C and APOA1 Gene rs1799837C>T Variants with Serum Lipid Profiles in Turkish Cypriot Patients with Coronary Artery Disease
dc.typeArticle

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