鉴定酒精依赖的基因变异。

IF 6.8 1区 医学 Q1 SUBSTANCE ABUSE
Alcohol Research : Current Reviews Pub Date : 2012-01-01
Arpana Agrawal, Laura J Bierut
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引用次数: 0

摘要

研究人员正在使用各种策略来识别可能与酗酒有关的基因。最初的努力主要依赖于候选基因和连锁研究;然而,最近,基因分型的现代进步导致了酒精依赖的全基因组关联研究的广泛使用。早期研究的主要发现是,编码酒精脱氢酶1B(即ADH1B基因)、醛脱氢酶2(即ALDH2基因)和其他酒精代谢酶的基因DNA序列的变异(即多态性)介导了酒精中毒的风险;此外,这些多态性也对与酒精有关的癌症(如食道癌)的风险有影响。此外,一种编码神经递质γ-氨基丁酸(GABA)受体的基因GABRA2似乎在酒精依赖的发展中起作用。现在,全基因组关联研究为发现酒精依赖的遗传病因和揭示新的治疗策略提供了大量新机会,同时也带来了挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identifying genetic variation for alcohol dependence.

Researchers are using various strategies to identify the genes that may be associated with alcoholism. The initial efforts primarily relied on candidate gene and linkage studies; more recently, however, modern advances in genotyping have resulted in widespread use of genome-wide association studies for alcohol dependence. The key findings of the earlier studies were that variations (i.e., polymorphisms) in the DNA sequences of the genes encoding alcohol dehydrogenase 1B (i.e., the ADH1B gene), aldehyde dehydrogenase 2 (i.e., the ALDH2 gene), and other alcohol-metabolizing enzymes mediate the risk for alcoholism; moreover, these polymorphisms also have an impact on the risk of alcohol-related cancers, such as esophageal cancer. In addition, a gene encoding one of the receptors for the neurotransmitter γ-aminobutyric acid (GABA) known as GABRA2 seems to have a role in the development of alcohol dependence. Genome-wide association studies now offer a host of emerging opportunities, as well as challenges, for discovering the genetic etiology of alcohol dependence and for unveiling new treatment strategies.

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来源期刊
自引率
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期刊介绍: Alcohol Research: Current Reviews (ARCR) is an open-access, peer-reviewed journal published by the National Institute on Alcohol Abuse and Alcoholism (NIAAA) at the National Institutes of Health. Starting from 2020, ARCR follows a continuous, rolling publication model, releasing one virtual issue per yearly volume. The journal offers free online access to its articles without subscription or pay-per-view fees. Readers can explore the content of the current volume, and past volumes are accessible in the journal's archive. ARCR's content, including previous titles, is indexed in PubMed, PsycINFO, Scopus, and Web of Science.
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