Birley Andrew J, James Michael R, Dickson Peter A, Montgomery Grant W, Heath Andrew C, Martin Nicholas G, Whitfield John B
Genetic Epidemiology Unit, Queensland Institute of Medical Research, PO Royal Brisbane Hospital, Brisbane, Queensland 4029, Australia.
Hum Mol Genet. 2009 Apr 15;18(8):1533-42. doi: 10.1093/hmg/ddp060. Epub 2009 Feb 4.
We have previously found that variation in alcohol metabolism in Europeans is linked to the chromosome 4q region containing the ADH gene family. We have now typed 103 single nucleotide polymorphisms (SNPs) across this region to test for allelic associations with variation in blood and breath alcohol concentrations after an alcohol challenge. In vivo alcohol metabolism was modelled with three parameters that identified the absorption and rise of alcohol concentration following ingestion, and the rate of elimination. Alleles of ADH7 SNPs were associated with the early stages of alcohol metabolism, with additional effects in the ADH1A, ADH1B and ADH4 regions. Rate of elimination was associated with SNPs in the intragenic region between ADH7 and ADH1C, and across ADH1C and ADH1B. SNPs affecting alcohol metabolism did not correspond to those reported to affect alcohol dependence or alcohol-related disease. The combined SNP associations with early- and late-stage metabolism only account for approximately 20% of the total genetic variance linked to the ADH region, and most of the variance for in vivo alcohol metabolism linked to this region is yet to be explained.
我们之前发现,欧洲人酒精代谢的差异与包含ADH基因家族的4号染色体q区域有关。我们现在对该区域的103个单核苷酸多态性(SNP)进行了分型,以检测在酒精激发后与血液和呼气酒精浓度变化的等位基因关联。体内酒精代谢用三个参数进行建模,这三个参数确定了摄入后酒精浓度的吸收和上升以及消除速率。ADH7 SNP的等位基因与酒精代谢的早期阶段相关,在ADH1A、ADH1B和ADH4区域还有额外影响。消除速率与ADH7和ADH1C之间基因内区域以及ADH1C和ADH1B之间的SNP相关。影响酒精代谢的SNP与那些据报道影响酒精依赖或酒精相关疾病的SNP并不对应。SNP与早期和晚期代谢的联合关联仅占与ADH区域相关的总遗传变异的约20%,与该区域相关的体内酒精代谢的大部分变异仍有待解释。