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荟萃分析:谷胱甘肽-S-转移酶等位基因变异与酒精性肝病相关。

Meta-analysis: glutathione-S-transferase allelic variants are associated with alcoholic liver disease.

机构信息

Department of Internal Medicine, Alcoholism Unit, University Hospital of Salamanca, Salamanca, Spain.

出版信息

Aliment Pharmacol Ther. 2011 Nov;34(10):1159-72. doi: 10.1111/j.1365-2036.2011.04862.x. Epub 2011 Oct 3.

Abstract

BACKGROUND

Only a minority of alcoholics develop alcoholic liver disease (ALD) and allelic variants within genes encoding glutathione-S-transferases (GST) have been associated with ALD vulnerability with controversial results.

AIM

To assess the effects of GST polymorphisms on ALD by means of a genetic association study and meta-analysis.

METHODS

We retrieved published studies on the relationship between allelic variants within GST genes and ALD by means of electronic database search. A meta-analysis was conducted in a fixed or random effects model. Calculations of odds ratios (OR) and their confidence intervals (CI), tests for heterogeneity of the results and sensitivity analysis, have been performed. A genetic association study comparing GSTM1, GSTT1 and GSTP1 genotype distribution among 279 alcoholics with or without ALD and 144 controls was also performed. Results  Fifteen previous studies were identified analysing the association of ALD with polymorphisms within GST genes. After meta-analysis, we found a significant association between the possession of the GSTM1 null allele and the presence of ALD (OR=1.43; 95% CI: 1.14, 1.78; P=0.002) among alcoholic patients. A significant association was also found for the possession of the GSTP1 Val/Val genotype and the presence of ALD (OR=2.04; 95% CI: 1.09, 3.80; P=0.03).

CONCLUSIONS

Our results suggest that, among alcoholics, carriers of GSTM1 null genetic variant or Val/Val genotype of Ile/Val GSTP1 polymorphism have an increased risk to suffer from alcoholic liver disease. The role of glutathione-S-transferase as a potential therapeutic target in alcoholic liver disease is reinforced.

摘要

背景

只有少数酗酒者会发展为酒精性肝病(ALD),而编码谷胱甘肽-S-转移酶(GST)的基因中的等位基因变异与 ALD 的易感性有关,但结果存在争议。

目的

通过遗传关联研究和荟萃分析评估 GST 多态性对 ALD 的影响。

方法

我们通过电子数据库检索检索了关于 GST 基因内等位基因变异与 ALD 之间关系的已发表研究。采用固定或随机效应模型进行荟萃分析。计算比值比(OR)及其置信区间(CI)、结果异质性检验和敏感性分析。还进行了一项比较 279 名患有或不患有 ALD 的酗酒者和 144 名对照者中 GSTM1、GSTT1 和 GSTP1 基因型分布的遗传关联研究。结果:共确定了 15 项先前的研究,分析了 GST 基因内多态性与 ALD 的相关性。荟萃分析后,我们发现 GSTM1 无效等位基因的存在与酗酒者 ALD 的发生之间存在显著相关性(OR=1.43;95%CI:1.14,1.78;P=0.002)。还发现 GSTP1 Ile/Val 多态性的 Val/Val 基因型的存在与 ALD 的发生之间存在显著相关性(OR=2.04;95%CI:1.09,3.80;P=0.03)。

结论

我们的结果表明,在酗酒者中,GSTM1 无效遗传变异或 GSTP1 Ile/Val 多态性的 Val/Val 基因型的携带者患酒精性肝病的风险增加。谷胱甘肽-S-转移酶作为酒精性肝病潜在治疗靶点的作用得到加强。

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