非酒精性脂肪肝患者PNPLA3 rs738409 C>G多态性的计算机和体外分析

Fatemeh Safari, Zeinab Imani-Saber, S. Mozafari, S. Lotfi, N. Einollahi
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摘要

背景:与肝脏脂肪含量相关的多态性被称为PNPLA3 rs738409 (Patatin-like phospholipase domain containing protein 3),是全球范围内研究非酒精性脂肪肝(NAFLD)患病率的关键课题之一。本研究旨在研究该多态性的生物信息学研究,并结合NAFLD患者的体外分析。材料与方法:在本病例对照研究中,在进行生物信息学分析后,分几个步骤进行实验室检查。从53例NAFLD患者和107例肝脏超声正常受试者的血液中提取基因组DNA。采用聚合酶链反应-限制性片段长度多态性方法对PNPLA3 rs738409进行基因分型。实验室检测结果包括空腹血糖、甘油三酯、胆固醇、高密度脂蛋白、低密度脂蛋白、丙氨酸转氨酶、天冬氨酸转氨酶。最后,采用SPSS 18.0版软件进行统计分析。结果:G等位基因在患者和对照组中的频率分别为56%和36%。患者和对照组基因型频率分别为35.8%和47.7% (CC)、17%和31.8% (CG)、47.2%和20.6% (GG)。GG和CG基因型的PNPLA3 rs738409 C>G校正优势比分别为3.0(95%可信区间[CI]: 1.28 ~ 6.98, P= 0.011)和0.68 (95% CI: 0.25 ~ 1.83, P= 0.44)。结论:GG基因型与NAFLD存在相关性。此外,生物信息学研究结果表明,氨基酸取代导致的亲水特性改变可能是疾病发生的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In Silico and In Vitro Analyses of PNPLA3 rs738409 C>G Polymorphism in Patients With Non-alcoholic Fatty Liver Disease
Background: The polymorphism associated with liver fat content, which is well-known as PNPLA3 rs738409 (Patatin-like phospholipase domain-containing protein 3), is one of the critical subjects widely investigated in the literature regarding the prevalence of non-alcoholic fatty liver disease (NAFLD) worldwide. The present research aimed to study the bioinformatics investigations of this polymorphism together with the in vitro analyses among patients with NAFLD. Materials and Methods: In this case-control study, after performing bioinformatics analysis, the laboratory examination was performed in several steps. Genomic DNA was extracted from the blood of 53 NAFLD patients and 107 subjects with normal liver ultrasounds. PNPLA3 rs738409 was genotyped by the polymerase chain reaction-restriction fragment length polymorphism method. The laboratory test results, including fasting blood sugar, triglyceride, cholesterol, high-density lipoprotein, low-density lipoprotein, alanine aminotransferase, and aspartate aminotransferase were collected from medical records. Finally, statistical analysis was performed using SPSS software, version 18.0. Results: The frequency of the G allele was 56% and 36% among patients and in the control group, respectively. The frequency of genotypes was 35.8% and 47.7% (CC), 17% and 31.8% (CG), 47.2% and 20.6% (GG) in patients and control groups, respectively. The adjusted odds ratios for PNPLA3 rs738409 C>G were 3.0 (95% confidence interval [CI]: 1.28-6.98, P=.011) and 0.68 (95% CI: 0.25- 1.83, P = .44) for GG and CG genotypes, respectively. Conclusion: The findings showed the association between the GG genotype and the presence of NAFLD. Furthermore, the bioinformatics findings suggested the probable risk of the disease incidence regarding the change of hydropathic characteristics resulting from the amino acid substitution.
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