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Genome-wide Association Study of Alcohol Dependence

全基因组关联研究 单核苷酸多态性 遗传关联 酒精依赖 遗传学 等位基因 生物 人口 医学 基因型 基因 生物化学 环境卫生
作者
Jens Treutlein,Sven Cichon,Monika Ridinger,Norbert Wodarz,Michael B. Soyka,Peter Zill,Wolfgang Maier,Rainald Moessner,Wolfgang Gäebel,Norbert Dahmen,Christoph Fehr,Norbert Scherbaum,Michael Steffens,Kerstin U. Ludwig,Josef Frank,H.-Erich Wichmann,Stefan Schreiber,Nico Dragano,Wolfgang H. Sommer,Fernando Leonardi‐Essmann
出处
期刊:Archives of General Psychiatry [American Medical Association]
卷期号:66 (7): 773-773 被引量:377
标识
DOI:10.1001/archgenpsychiatry.2009.83
摘要

Context

Alcohol dependence is a serious and common public health problem. It is well established that genetic factors play a major role in the development of this disorder. Identification of genes that contribute to alcohol dependence will improve our understanding of the mechanisms that underlie this disorder.

Objective

To identify susceptibility genes for alcohol dependence through a genome-wide association study (GWAS) and a follow-up study in a population of German male inpatients with an early age at onset.

Design

The GWAS tested 524 396 single-nucleotide polymorphisms (SNPs). All SNPs withP < 10−4were subjected to the follow-up study. In addition, nominally significant SNPs from genes that had also shown expression changes in rat brains after long-term alcohol consumption were selected for the follow-up step.

Setting

Five university hospitals in southern and central Germany.

Participants

The GWAS included 487 male inpatients with alcohol dependence as defined by theDSM-IVand an age at onset younger than 28 years and 1358 population-based control individuals. The follow-up study included 1024 male inpatients and 996 age-matched male controls. All the participants were of German descent.

Main Outcome Measures

Significant association findings in the GWAS and follow-up study with the same alleles.

Results

The GWAS produced 121 SNPs with nominalP < 10−4. These, together with 19 additional SNPs from homologues of rat genes showing differential expression, were genotyped in the follow-up sample. Fifteen SNPs showed significant association with the same allele as in the GWAS. In the combined analysis, 2 closely linked intergenic SNPs met genome-wide significance (rs7590720,P = 9.72 × 10−9; rs1344694,P = 1.69 × 10−8). They are located on chromosome region 2q35, which has been implicated in linkage studies for alcohol phenotypes. Nine SNPs were located in genes, including theCDH13andADH1Cgenes, that have been reported to be associated with alcohol dependence.

Conclusions

This is the first GWAS and follow-up study to identify a genome-wide significant association in alcohol dependence. Further independent studies are required to confirm these findings.

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