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外源性代谢酶(GSTM1 和 GSTT1)和促炎细胞因子(TNF-α 和 IL-6)基因多态性与非酒精性脂肪性肝病的关系。

Association of xenobiotic-metabolizing enzymes (GSTM1 and GSTT 1), and pro-inflammatory cytokines (TNF-α and IL-6) genetic polymorphisms with non-alcoholic fatty liver disease.

机构信息

Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran.

Dr. Zeinali's Medical Genetics Laboratory, Kawsar Human Genetics Research Center, Tehran, Iran.

出版信息

Mol Biol Rep. 2021 Feb;48(2):1225-1231. doi: 10.1007/s11033-021-06142-1. Epub 2021 Jan 25.

Abstract

Previous studies have revealed that genetic polymorphisms of the Glutathione S-transferase M1 and T1 (GSTM1 and GSTT1), tumor necrosis factor-α (TNF-α), and interleukin 6 (IL-6) are associated with the presence of non-alcoholic fatty liver disease (NAFLD) in many populations. This study was conducted to investigate the association of the GSTM1, GSTT1, TNF-α rs1800629, and IL-6 rs1800795 with NAFLD in the general Iranian population. A case-control analysis included 242 NAFLD patients and 324 healthy controls from Iranian adults. After the physical examination, the genotypes were determined by polymerase chain reaction(PCR). The GSTM1 null, GSTT1 null, TNF-α AG/AA, and IL-6 CG/CC genotypes were deemed to be high-risk. The null allele of GSTM1 and A allele of TNF-α were more frequent in NAFLD patients even after Bonferroni's correction (P values<0.005, adjusted odds ratio (OR), 1.66 and 2.02; 95% confidence intervals (CI), (1.18-2.32) and (1.34-3.34), respectively. The IL-6 CC/CG genotype association with NAFLD was not significant after correction (P value = 0.04) Polymorphisms of xenobiotic and pro-inflammatory genes are associated with NAFLD in the Iranian population and seem to be a useful tool for NAFLD prevention and care.

摘要

先前的研究表明,谷胱甘肽 S-转移酶 M1 和 T1(GSTM1 和 GSTT1)、肿瘤坏死因子-α(TNF-α)和白细胞介素 6(IL-6)的遗传多态性与许多人群中非酒精性脂肪性肝病(NAFLD)的存在有关。本研究旨在探讨 GSTM1、GSTT1、TNF-α rs1800629 和 IL-6 rs1800795 与伊朗普通人群中 NAFLD 的相关性。一项病例对照分析纳入了 242 名 NAFLD 患者和 324 名来自伊朗成年人的健康对照者。体检后,通过聚合酶链反应(PCR)确定基因型。GSTM1 缺失型、GSTT1 缺失型、TNF-α AG/AA 和 IL-6 CG/CC 基因型被认为是高危型。即使经过 Bonferroni 校正,NAFLD 患者的 GSTM1 缺失等位基因和 TNF-α 的 A 等位基因更为常见(P 值均<0.005,校正后的比值比(OR)分别为 1.66 和 2.02;95%置信区间(CI)分别为(1.18-2.32)和(1.34-3.34))。IL-6 CC/CG 基因型与 NAFLD 的相关性在校正后不显著(P 值=0.04)。外源性和促炎基因的多态性与伊朗人群中的 NAFLD 相关,似乎是预防和治疗 NAFLD 的有用工具。

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