一项关于酒精依赖的全基因组关联研究。

A genome-wide association study of alcohol dependence.

机构信息

Department of Psychiatry, Washington University School of Medicine, St Louis, MO 63110, USA.

出版信息

Proc Natl Acad Sci U S A. 2010 Mar 16;107(11):5082-7. doi: 10.1073/pnas.0911109107. Epub 2010 Mar 2.

Abstract

Excessive alcohol consumption is one of the leading causes of preventable death in the United States. Approximately 14% of those who use alcohol meet criteria during their lifetime for alcohol dependence, which is characterized by tolerance, withdrawal, inability to stop drinking, and continued drinking despite serious psychological or physiological problems. We explored genetic influences on alcohol dependence among 1,897 European-American and African-American subjects with alcohol dependence compared with 1,932 unrelated, alcohol-exposed, nondependent controls. Constitutional DNA of each subject was genotyped using the Illumina 1M beadchip. Fifteen SNPs yielded P < 10(-5), but in two independent replication series, no SNP passed a replication threshold of P < 0.05. Candidate gene GABRA2, which encodes the GABA receptor alpha2 subunit, was evaluated independently. Five SNPs at GABRA2 yielded nominal (uncorrected) P < 0.05, with odds ratios between 1.11 and 1.16. Further dissection of the alcoholism phenotype, to disentangle the influence of comorbid substance-use disorders, will be a next step in identifying genetic variants associated with alcohol dependence.

摘要

过量饮酒是美国可预防死亡的主要原因之一。大约有 14%的饮酒者在其一生中符合酒精依赖的标准,其特征为耐受、戒断、无法停止饮酒以及尽管存在严重的心理或生理问题仍继续饮酒。我们比较了 1897 名欧洲裔美国人和非裔美国酒精依赖患者与 1932 名无血缘关系、酒精暴露、无依赖对照者,探讨了遗传因素对酒精依赖的影响。每位受试者的结构 DNA 均使用 Illumina 1M 珠芯片进行基因分型。有 15 个 SNP 达到 P < 10(-5),但在两个独立的复制系列中,没有 SNP 通过 P < 0.05 的复制阈值。候选基因 GABRA2,其编码 GABA 受体 alpha2 亚单位,被独立评估。GABRA2 有 5 个 SNP 达到名义(未校正)P < 0.05,比值比在 1.11 至 1.16 之间。进一步剖析酒精中毒表型,以区分合并物质使用障碍的影响,将是确定与酒精依赖相关的遗传变异体的下一步。

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