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土耳其裔非酒精性脂肪性肝炎患者中 CYP2E1、GCKR 和 PNPLA3 的基因型变异。

Genotypic variation in CYP2E1, GCKR, and PNPLA3 among nonalcoholic steatohepatitis patients of Turkish origin.

机构信息

Life Science, and Biomedical Engineering Application and Research Center, Istanbul Gelisim University, Istanbul, 34310, Turkey.

Vocational School of health services, Istanbul Gelisim University, Istanbul, 34310, Turkey.

出版信息

Mol Biol Rep. 2024 Jul 23;51(1):845. doi: 10.1007/s11033-024-09787-w.

Abstract

BACKGROUND

This study examines genetic variations in CYP2E1 (rs6413432, rs3813867), GCKR (rs780094, rs1260326), and PNPLA3 (rs738409) among Turkish patients to assess their influence on nonalcoholic steatohepatitis.

METHODS

Allele 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.

RESULTS

No 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.

CONCLUSIONS

Variants 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.

摘要

背景

本研究旨在探讨 CYP2E1(rs6413432、rs3813867)、GCKR(rs780094、rs1260326)和 PNPLA3(rs738409)在土耳其患者中的基因变异情况,以评估其对非酒精性脂肪性肝炎的影响。

方法

通过聚合酶链反应-限制性片段长度多态性 SNP 基因分型,比较 245 例 NASH 患者和 120 例健康对照者的等位基因和基因型频率。此外,还检查了观察到的基因型频率与 Hardy-Weinberg 比例的偏差。

结果

NASH 患者和健康对照组之间,rs6413432、rs3813867 和 rs780094 的等位基因和基因型分布无显著差异。然而,rs1260326 和 rs738409 的分布存在显著差异。性别和年龄特异性分布无明显差异。唯一观察到的偏离 Hardy-Weinberg 比例的是 rs738409 的基因型频率。

结论

GCKR(rs1260326)和 PNPLA3(rs738409)的变异与土耳其人群 NASH 风险增加显著相关,其中 rs738409 变异可能在 NASH 发病机制中发挥更重要的作用。

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