Institute of Psychiatric Research, Department of Psychiatry, School of Medicine, Indiana University, 320 W. 15th Street, Indianapolis, IN, 46202, USA,
Curr Psychiatry Rep. 2014 Dec;16(12):518. doi: 10.1007/s11920-014-0518-0.
Alcohol use and alcohol use disorders are substantially heritable. Variants in genes coding for alcohol metabolic enzymes have long been known to influence consumption. More recent studies in family-based samples have implicated GABRA2, nicotinic receptor genes such as CHRNB3, and a number of other specific single genes as associated with alcohol use disorders. The growing use of genetic analyses, in particular studies using polygenic risk scores; neurobiologic pathways; and methods for quantifying gene × gene and gene × environment interactions have also contributed to an evolving understanding of the genetic architecture of alcohol use disorders. Additionally, the study of behavioral traits associated with alcohol dependence such as impulsivity and sensation seeking, and the influences of demographic factors (i.e., sex and ethnicity) have significantly enhanced the genetics of alcoholism literature. This article provides a brief overview of the current topically relevant findings in the field to date and includes areas of research still requiring attention.
饮酒和酒精使用障碍在很大程度上是可遗传的。长期以来,编码酒精代谢酶的基因变异被认为会影响酒精的摄入。最近在基于家族的样本中的研究表明,GABRA2、尼古丁受体基因(如 CHRNB3)和许多其他特定的单基因与酒精使用障碍有关。遗传分析的广泛应用,特别是使用多基因风险评分、神经生物学途径和量化基因-基因和基因-环境相互作用的方法,也促进了对酒精使用障碍遗传结构的不断认识。此外,对与酒精依赖相关的行为特征(如冲动性和寻求刺激)以及人口因素(即性别和种族)的研究,极大地丰富了酒精中毒文献的遗传学内容。本文简要概述了迄今为止该领域目前相关的发现,并包括仍需要关注的研究领域。