Treutlein Jens, Cichon Sven, Ridinger Monika, Wodarz Norbert, Soyka Michael, Zill Peter, Maier Wolfgang, Moessner Rainald, Gaebel Wolfgang, Dahmen Norbert, Fehr Christoph, Scherbaum Norbert, Steffens Michael, Ludwig Kerstin U, Frank Josef, Wichmann H Erich, Schreiber Stefan, Dragano Nico, Sommer Wolfgang H, Leonardi-Essmann Fernando, Lourdusamy Anbarasu, Gebicke-Haerter Peter, Wienker Thomas F, Sullivan Patrick F, Nöthen Markus M, Kiefer Falk, Spanagel Rainer, Mann Karl, Rietschel Marcella
Department of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Mannheim, Germany.
Arch Gen Psychiatry. 2009 Jul;66(7):773-84. doi: 10.1001/archgenpsychiatry.2009.83.
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.
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.
The GWAS tested 524,396 single-nucleotide polymorphisms (SNPs). All SNPs with P < 10(-4) were 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.
Five university hospitals in southern and central Germany.
The GWAS included 487 male inpatients with alcohol dependence as defined by the DSM-IV and 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.
Significant association findings in the GWAS and follow-up study with the same alleles.
The GWAS produced 121 SNPs with nominal P < 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 x 10(-9); rs1344694, P = 1.69 x 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 the CDH13 and ADH1C genes, that have been reported to be associated with alcohol dependence.
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.
酒精依赖是一个严重且常见的公共卫生问题。众所周知,遗传因素在这种疾病的发展中起主要作用。识别导致酒精依赖的基因将增进我们对该疾病潜在机制的理解。
通过全基因组关联研究(GWAS)以及对一群发病年龄较早的德国男性住院患者进行后续研究,来识别酒精依赖的易感基因。
GWAS检测了524,396个单核苷酸多态性(SNP)。所有P<10^(-4)的SNP都进入后续研究。此外,还选择了来自长期饮酒后大鼠大脑中也显示出表达变化的基因的名义上显著的SNP进行后续研究。
德国南部和中部的五所大学医院。
GWAS纳入了487名符合DSM-IV定义的酒精依赖男性住院患者,发病年龄小于28岁,以及1358名基于人群的对照个体。后续研究纳入了1024名男性住院患者和996名年龄匹配的男性对照。所有参与者均为德国血统。
GWAS和后续研究中与相同等位基因的显著关联结果。
GWAS产生了121个名义P<10^(-4)的SNP。这些SNP以及另外19个来自显示差异表达的大鼠基因同源物的SNP在后续样本中进行了基因分型。15个SNP显示出与GWAS中相同的等位基因有显著关联。在综合分析中,2个紧密连锁的基因间SNP达到全基因组显著性水平(rs7590720,P = 9.72×10^(-9);rs1344694,P = 1.69×10^(-8))。它们位于2q35染色体区域,该区域在酒精表型的连锁研究中已有涉及。9个SNP位于基因中,包括已报道与酒精依赖相关的CDH13和ADH1C基因。
这是首次在酒精依赖中识别出全基因组显著关联的GWAS及后续研究。需要进一步的独立研究来证实这些发现。