Foroud Tatiana, Wetherill Leah Flury, Dick Danielle M, Hesselbrock Victor, Nurnberger John I, Kramer John, Tischfield Jay, Schuckit Marc, Bierut Laura J, Xuei Xiaoling, Edenberg Howard J
Indiana University School of Medicine, Indianapolis, Indiana 46202-3002, USA.
Alcohol Clin Exp Res. 2007 Nov;31(11):1773-9. doi: 10.1111/j.1530-0277.2007.00505.x. Epub 2007 Sep 11.
To test whether variation in the gene encoding the enzyme catechol-O-methyltransferase (COMT), which catalyzes the breakdown of dopamine and other catecholamine neurotransmitters, is associated with the risk for alcohol dependence and habitual smoking.
Single nucleotide polymophisms (SNPs) were genotyped in a sample of 219 multiplex alcohol-dependent families of European American descent from the Collaborative Study on the Genetics of Alcoholism (COGA). Family-based tests of association were performed to evaluate the evidence of association between the 18 SNPs distributed throughout COMT, including the functional Val158Met polymorphism, and the phenotypes of alcohol dependence, early onset alcohol dependence, habitual smoking, and comorbid alcohol dependence and habitual smoking.
No significant, consistent evidence of association was found with alcohol dependence, early onset alcohol dependence, habitual smoking or the comorbid phenotype. There was no evidence that the functional Val158Met polymorphism, previously reported to be associated with these phenotypes, was associated with any of them.
Despite the substantial size of this study, we did not find evidence to support an association between alcohol dependence or habitual smoking and variation in COMT.
测试编码儿茶酚-O-甲基转移酶(COMT)的基因变异是否与酒精依赖和习惯性吸烟风险相关,该酶催化多巴胺和其他儿茶酚胺神经递质的分解。
在酒精中毒遗传学合作研究(COGA)中,对219个欧美裔多重酒精依赖家庭样本进行单核苷酸多态性(SNP)基因分型。进行基于家庭的关联测试,以评估分布在整个COMT中的18个SNP(包括功能性Val158Met多态性)与酒精依赖、早发性酒精依赖、习惯性吸烟以及酒精依赖与习惯性吸烟共病表型之间的关联证据。
未发现与酒精依赖、早发性酒精依赖、习惯性吸烟或共病表型有显著、一致的关联证据。没有证据表明先前报道与这些表型相关的功能性Val158Met多态性与其中任何一种有关。
尽管本研究规模较大,但我们未找到证据支持酒精依赖或习惯性吸烟与COMT变异之间存在关联。