Muramatsu T, Higuchi S
National Institute on Alcoholism, Kurihama National Hospital, Kanagawa, Japan.
Biochem Biophys Res Commun. 1995 Jun 6;211(1):28-32. doi: 10.1006/bbrc.1995.1773.
In this search for a possible association between the dopamine transporter gene (DAT1) polymorphism and alcoholism, 655 Japanese alcoholics were grouped according to their aldehyde dehydrogenase-2 (ALDH2) genotypes. Because inactive ALDH2 is an established negative risk factor for alcoholism, alcoholics with the mutant allele, ALDH22, were considered a relatively homogeneous group. The frequency of the 7-repeat allele of the DAT1 variable number of tandem repeat was significantly higher in alcoholics with ALDH22 than in control subjects. These results are consistent with the hypothesis that alteration in the dopaminergic system plays some role in the development of alcoholism.
在探索多巴胺转运体基因(DAT1)多态性与酒精中毒之间可能存在的关联时,655名日本酗酒者根据其乙醛脱氢酶2(ALDH2)基因型进行了分组。由于无活性的ALDH2是已确定的酒精中毒负性风险因素,携带突变等位基因ALDH22的酗酒者被视为一个相对同质的群体。DAT1可变串联重复序列7次重复等位基因的频率在携带ALDH22的酗酒者中显著高于对照组。这些结果与多巴胺能系统改变在酒精中毒发展中起一定作用的假说一致。