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首页> 外文期刊>Psychiatric genetics >Genetic polymorphisms of the promoter region of dopamine D2 receptor and dopamine transporter genes and alcoholism among four aboriginal groups and Han Chinese in Taiwan.
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Genetic polymorphisms of the promoter region of dopamine D2 receptor and dopamine transporter genes and alcoholism among four aboriginal groups and Han Chinese in Taiwan.

机译:台湾四个原住民群体和汉族人群中多巴胺D2受体和多巴胺转运蛋白基因的启动子区域遗传多态性与酒精中毒。

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摘要

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.
机译:这项研究旨在检验多巴胺D2受体(DRD2)基因启动子区域的功能多态性(即-141C Ins / Del)与多巴胺转运蛋白3'非翻译区的可变数目的串联重复多态性之间的关系( DAT)基因(SLC6A3)与酒精中毒的病例对照研究中。病例(n = 203)为酒精中毒且有戒断症状的患者,对照组(n = 213)为性别和种族相匹配的个体,这些个体经过筛查以排除四个原住民群体(Atayal,Ami,Bunun,和排湾)和台湾的汉族。为了控制潜在的混杂因素,在部分分析中,我们从控制对象中排除了烟草滥用者,并比较了具有严重医疗并发症的酗酒者和较轻医疗并发症的酗酒者的遗传多态性分布。在这五个不同种族的饮酒者和对照组之间,这两个不同遗传标记的等位基因和基因型频率没有差异。 -141C多态性与另外两个DRD2多态性(TaqI A和NcoI)之间没有显着的连锁不平衡。当病例仅限于酒精中毒且具有更严重的医疗并发症时,或将吸烟者排除在控制对象之外时,结果仍保持不变。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。

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