Husseini, Abbas Ali2024-09-112024-09-1120240301-48511573-4978https://doi.org/10.1007/s11033-024-09787-whttps://hdl.handle.net/11363/7617BackgroundThis study examines genetic variations in CYP2E1 (rs6413432, rs3813867), GCKR (rs780094, rs1260326), and PNPLA3 (rs738409) among Turkish patients to assess their influence on nonalcoholic steatohepatitis.MethodsAllele and genotype frequencies were compared between 245 NASH patients and 120 healthy controls using SNP genotyping via polymerase chain reaction-restriction fragment length polymorphism. Additionally, the deviation of the observed genotype frequencies from Hardy-Weinberg proportion was examined.ResultsNo significant differences were found in the allelic and genotypic distributions of rs6413432, rs3813867, and rs780094 between NASH patients and healthy controls. However, significant disparities were noted for rs1260326 and rs738409. Gender and age-specific distributions showed no notable differences. The only observed deviation from Hardy-Weinberg proportion was in the genotype frequency of rs738409.ConclusionsVariants in GCKR (rs1260326) and PNPLA3 (rs738409) are significantly associated with increased NASH risk in the Turkish population, with the rs738409 variant potentially playing a more prominent role in NASH development.eninfo:eu-repo/semantics/closedAccessSingle nucleotide polymorphismNonalcoholic steatohepatitisTurkish populationHardy-Weinberg proportionArticle51110.1007/s11033-024-09787-w390422592-s2.0-85199302723WOS:001275388500010N/A