Alcohol dehydrogenase 1C (ADH1C) gene polymorphism and alcoholic liver cirrhosis risk: a meta analysis.

IF 0.2 Q4 MEDICINE, RESEARCH & EXPERIMENTAL International journal of clinical and experimental medicine Pub Date : 2015-07-15 eCollection Date: 2015-01-01
Lei He, Tao Deng, He-Sheng Luo
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Abstract

The association between alcohol dehydrogenase 1C (ADH1C) gene polymorphism and alcoholic liver cirrhosis (ALC) has been analyzed in several studies, but results have been conflicting. In this study, a meta-analysis was performed to assess the associations between the ADH1C polymorphism and risk of ALC. Relevant studies were identified using PubMed, Web of Science, CNKI and Wanfang databases up to January 10, 2015. Odds ratios (ORs) and 95% confidence intervals (CIs) were used to assess the strength of the association using the fixed or random effect model. A total of 16 case-control studies, including 1375 cases and 1802 controls, were included. Overall, no significant association between the ADH1C polymorphism and ALC risk was found (dominant model: OR=0.87, 95% CI: 0.62-1.23; recessive model: OR=1.30, 95% CI: 0.84-1.99; *1/*2 vs. *1/*1: OR=0.87, 95% CI: 0.63-1.21; *2/*2 vs. *1/*1: OR=1.10, 95% CI: 0.71-1.70). In the subgroup analysis by ethnicity, we observed a significant association in Asian descent (*1/*2 vs. *1/*1: OR=1.63, 95% CI: 1.07-2.49), while a decreased risk was found among Caucasians (dominant model: OR=0.81, 95% CI: 0.66-0.99; *1/*2 vs. *1/*1: OR=0.76, 95% CI: 0.61-0.95). This meta-analysis demonstrated that the ADH1C polymorphism might increase the risk of ALC in Asians, while it may be a protective factor for ALC among Caucasians.

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酒精脱氢酶1C (ADH1C)基因多态性与酒精性肝硬化风险的meta分析
一些研究分析了酒精脱氢酶1C (ADH1C)基因多态性与酒精性肝硬化(ALC)之间的关系,但结果相互矛盾。在这项研究中,进行了一项荟萃分析,以评估ADH1C多态性与ALC风险之间的关系。截至2015年1月10日,检索PubMed、Web of Science、CNKI、万方等数据库。比值比(ORs)和95%置信区间(CIs)采用固定或随机效应模型评估关联强度。共纳入16项病例对照研究,包括1375例病例和1802例对照。总体而言,ADH1C多态性与ALC风险之间未发现显著关联(优势模型:OR=0.87, 95% CI: 0.62-1.23;隐性模型:OR=1.30, 95% CI: 0.84-1.99;*1/*2 vs. *1/*1: OR=0.87, 95% CI: 0.63-1.21;*2/*2 vs. *1/*1: OR=1.10, 95% CI: 0.71-1.70)。在按种族划分的亚组分析中,我们观察到亚洲血统有显著的相关性(*1/*2 vs *1/*1: OR=1.63, 95% CI: 1.07-2.49),而白种人的风险较低(优势模型:OR=0.81, 95% CI: 0.66-0.99;*1/*2 vs. *1/*1: OR=0.76, 95% CI: 0.61-0.95)。该荟萃分析表明,ADH1C多态性可能增加亚洲人患ALC的风险,而它可能是白种人患ALC的保护因素。
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