Chen W J, Chen C H, Huang J, Hsu Y P, Seow S V, Chen C C, Cheng A T
Institute of Epidemiology, College of Public Health, National Taiwan University, Taipei, Taiwan.
Psychiatr Genet. 2001 Dec;11(4):187-95. doi: 10.1097/00041444-200112000-00002.
This study aims to examine the relationship between the functional polymorphism at the promoter region of the dopamine D2 receptor (DRD2) gene (i.e. -141C Ins/Del) and variable number of tandem repeat polymorphism at the 3' untranslated region of the dopamine transporter (DAT) gene (SLC6A3) with alcoholism in a case-control study. The cases (n = 203) were alcohol dependents with withdrawal symptoms, and the controls (n = 213) were sex- and ethnicity-matched individuals who were screened to exclude those with alcohol problems among four aboriginal groups (Atayal, Ami, Bunun, and Paiwan) and Han Chinese in Taiwan. To control for potential confounding factors, we excluded tobacco abusers from control subjects in part of the analysis and compared the distribution of the genetic polymorphisms in alcoholics with severe medical complications versus those with less severe medical complications. There were no differences in allele and genotype frequencies of these two distinct genetic markers between alcoholics and control subjects in these five different ethnic groups. There was no significant linkage disequilibrium between the -141C polymorphism and two other DRD2 polymorphisms (TaqI A and NcoI). The results remained unchanged when cases were limited to alcoholics with more severe medical complications or when tobacco abusers were excluded from control subjects. The results suggest that both the DRD2 promoter region and the DAT gene do not play a significant role in conferring vulnerability to alcoholism.
本研究旨在通过一项病例对照研究,探讨多巴胺D2受体(DRD2)基因启动子区域的功能多态性(即-141C插入/缺失)与多巴胺转运体(DAT)基因(SLC6A3)3'非翻译区串联重复多态性的可变数目与酒精中毒之间的关系。病例组(n = 203)为有戒断症状的酒精依赖者,对照组(n = 213)为性别和种族匹配的个体,这些个体在台湾的四个原住民群体(泰雅族、阿美族、布农族和排湾族)以及汉族中经过筛查以排除有酒精问题的人。为控制潜在的混杂因素,在部分分析中我们从对照组中排除了烟草滥用者,并比较了患有严重医学并发症的酗酒者与患有较轻医学并发症的酗酒者之间基因多态性的分布。在这五个不同种族群体中,酗酒者与对照组之间这两种不同基因标记的等位基因和基因型频率没有差异。-141C多态性与其他两个DRD2多态性(TaqI A和NcoI)之间没有显著的连锁不平衡。当病例仅限于患有更严重医学并发症的酗酒者时,或者当从对照组中排除烟草滥用者时,结果保持不变。结果表明,DRD2启动子区域和DAT基因在赋予酒精中毒易感性方面均不发挥重要作用。