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成瘾的人类遗传学:新的见解和未来方向。

Human Genetics of Addiction: New Insights and Future Directions.

机构信息

Behavioral and Urban Health Program, Behavioral Health and Criminal Justice Division, RTI International, 3040 East Cornwallis Road, P. O. Box 12194, Research Triangle Park, NC, 27709, USA.

Department of Psychiatry, Washington University, St. Louis, MO, USA.

出版信息

Curr Psychiatry Rep. 2018 Mar 5;20(2):8. doi: 10.1007/s11920-018-0873-3.

Abstract

PURPOSE OF REVIEW

With the advent of the genome-wide association study (GWAS), our understanding of the genetics of addiction has made significant strides forward. Here, we summarize genetic loci containing variants identified at genome-wide statistical significance (P < 5 × 10) and independently replicated, review evidence of functional or regulatory effects for GWAS-identified variants, and outline multi-omics approaches to enhance discovery and characterize addiction loci.

RECENT FINDINGS

Replicable GWAS findings span 11 genetic loci for smoking, eight loci for alcohol, and two loci for illicit drugs combined and include missense functional variants and noncoding variants with regulatory effects in human brain tissues traditionally viewed as addiction-relevant (e.g., prefrontal cortex [PFC]) and, more recently, tissues often overlooked (e.g., cerebellum). GWAS analyses have discovered several novel, replicable variants contributing to addiction. Using larger sample sizes from harmonized datasets and new approaches to integrate GWAS with multiple 'omics data across human brain tissues holds great promise to significantly advance our understanding of the biology underlying addiction.

摘要

目的综述:随着全基因组关联研究(GWAS)的出现,我们对成瘾遗传学的理解取得了重大进展。在这里,我们总结了包含在全基因组统计学意义上(P < 5×10)独立复制的变异体的遗传位点,回顾了 GWAS 鉴定的变异体的功能或调节效应的证据,并概述了多组学方法,以增强发现和描述成瘾基因座。

最新发现:可复制的 GWAS 发现跨越了 11 个与吸烟相关的遗传位点、8 个与酒精相关的遗传位点和 2 个与非法药物相关的遗传位点,包括错义功能变异体和具有调节作用的非编码变异体,这些变异体在传统上被认为与成瘾相关的人类脑组织(例如前额叶皮层 [PFC])中,以及最近在经常被忽视的组织(例如小脑)中。GWAS 分析发现了几个新的、可复制的与成瘾相关的变异体。利用来自协调数据集的更大样本量和新方法将 GWAS 与人类脑组织的多种“组学”数据整合起来,有望极大地促进我们对成瘾生物学基础的理解。

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