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肿瘤坏死因子启动子多态性与酒精性脂肪性肝炎易感性的关联。

Association of a tumor necrosis factor promoter polymorphism with susceptibility to alcoholic steatohepatitis.

作者信息

Grove J, Daly A K, Bassendine M F, Day C P

机构信息

Department of Medicine, University of Newcastle, Newcastle upon Tyne, UK.

出版信息

Hepatology. 1997 Jul;26(1):143-6. doi: 10.1002/hep.510260119.

Abstract

Twin concordance studies suggest that genetic factors play a role in determining why only a minority of heavy drinkers develop hepatitis and cirrhosis. Tumor necrosis factor alpha (TNF-alpha) has emerged as the "final common pathway" in the pathogenesis of alcohol-related hepatic necro-inflammation. We have examined the frequency of the two recently described polymorphisms of the TNF-alpha promoter in 150 patients with biopsy-proven alcoholic liver disease and 145 healthy volunteers. There was a significant excess of the rare allele (TNFA-A; G(-238) --> A) at position -238 in patients with steatohepatitis compared with controls or patients without this lesion. This is consistent with previous suggestions that the TNFA-A allele, which falls within a putative Y regulation box of the TNF-alpha promoter, is associated with increased TNF-alpha expression. No differences were observed for the polymorphism at position -308.

摘要

双生子一致性研究表明,遗传因素在决定为何仅有少数重度饮酒者会发展为肝炎和肝硬化方面发挥作用。肿瘤坏死因子α(TNF-α)已成为酒精性肝坏死炎症发病机制中的“最终共同通路”。我们检测了150例经活检证实为酒精性肝病的患者及145名健康志愿者中最近描述的两种TNF-α启动子多态性的频率。与对照组或无此病变的患者相比,脂肪性肝炎患者中-238位点的罕见等位基因(TNFA-A;G(-238)→A)显著增多。这与之前的观点一致,即位于TNF-α启动子假定的Y调控框内的TNFA-A等位基因与TNF-α表达增加有关。在-308位点的多态性方面未观察到差异。

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