Kuo Po-Hsiu, Kalsi Gursharan, Prescott Carol A, Hodgkinson Colin A, Goldman David, van den Oord Edwin J, Alexander Jeffry, Jiang Cizhong, Sullivan Patrick F, Patterson Diana G, Walsh Dermot, Kendler Kenneth S, Riley Brien P
Institute of Clinical Medicine, College of Medicine, National Cheng Kung University Hospital 138, National Cheng Kung University, Sheng-Li Road, Tainan 704, Taiwan.
Alcohol Clin Exp Res. 2008 May;32(5):785-95. doi: 10.1111/j.1530-0277.2008.00642.x. Epub 2008 Mar 4.
The genes coding for ethanol metabolism enzymes [alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH)] have been widely studied for their influence on the risk to develop alcohol dependence (AD). However, the relation between polymorphisms of these metabolism genes and AD in Caucasian subjects has not been clearly established. The present study examined evidence for the association of alcohol metabolism genes with AD in the Irish Affected Sib Pair Study of alcohol dependence.
We conducted a case-control association study with 575 independent subjects who met Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, AD diagnosis and 530 controls. A total of 77 single nucleotide polymorphisms (SNPs) in the seven ADH (ADH1-7) and two ALDH genes (ALDH1A1 and ALDH2) were genotyped using the Illumina GoldenGate protocols. Several statistical procedures were implemented to control for false discoveries.
All markers with minor allele frequency greater than 0.01 were in Hardy-Weinberg equilibrium. Numerous SNPs in ADH genes showed association with AD, including one marker in the coding region of ADH1C (rs1693482 in exon6, Ile271Gln). Haplotypic association was observed in the ADH5 and ADH1C genes, and in a long haplotype block formed by the ADH1A and ADH1B loci. We detected two significant interactions between pairs of markers in intron 6 of ADH6 and intron 12 of ALDH2 (p = 5 x 10(-5)), and 5' of both ADH4 and ADH1A (p = 2 x 10(-4)).
We found evidence for the association of several ADH genes with AD in a sample of Western European origin. The significant interaction effects between markers in ADH and ALDH genes suggest possible epistatic roles between alcohol metabolic enzymes in the risk for AD.
编码乙醇代谢酶[酒精脱氢酶(ADH)和乙醛脱氢酶(ALDH)]的基因因其对酒精依赖(AD)发生风险的影响而受到广泛研究。然而,这些代谢基因的多态性与白种人AD之间的关系尚未明确确立。本研究在爱尔兰酒精依赖同胞对研究中检验了酒精代谢基因与AD关联的证据。
我们对575名符合《精神疾病诊断与统计手册》第4版AD诊断标准的独立受试者和530名对照进行了病例对照关联研究。使用Illumina GoldenGate方案对7个ADH基因(ADH1 - 7)和2个ALDH基因(ALDH1A1和ALDH2)中的总共77个单核苷酸多态性(SNP)进行基因分型。实施了几种统计程序以控制假发现。
所有次要等位基因频率大于0.01的标记均处于哈迪 - 温伯格平衡。ADH基因中的许多SNP显示与AD相关,包括ADH1C编码区的一个标记(外显子6中的rs1693482,Ile271Gln)。在ADH5和ADH1C基因以及由ADH1A和ADH1B位点形成的一个长单倍型块中观察到单倍型关联。我们在ADH6内含子6和ALDH2内含子12的标记对之间(p = 5×10^(-5))以及ADH4和ADH1A两者的5'端(p = 2×10^(-4))检测到两个显著的相互作用。
我们在一个西欧血统样本中发现了几个ADH基因与AD关联的证据。ADH和ALDH基因中标记之间的显著相互作用效应表明酒精代谢酶在AD风险中可能存在上位性作用。