Kranzler Henry, Lappalainen Jaakko, Nellissery Maggie, Gelernter Joel
Department of Psychiatry, Alchohol Research Center, university of Connecticut School of Medicine, Farmington, Connecticult 06030-2103, USA.
Alcohol Clin Exp Res. 2002 Sep;26(9):1330-5. doi: 10.1097/01.ALC.0000030840.48315.40.
Association studies of a reportedly functional polymorphism in the promoter region (5'-HTTLPR) of the gene encoding the serotonin transporter protein (genetic locus SLC6A4) in alcoholics have yielded conflicting results. The most frequently observed alleles of the 5'-HTTLPR polymorphism are the short and long variants; the short variant is associated with lower transcriptional activity of the SLC6A4 gene than is the long variant. To reduce the heterogeneity that may confound association studies of alcohol dependence, we examined the association of 5'-HTTLPR alleles with three dichotomous typologies of alcoholism based on sex, comorbid drug dependence, or age of onset of alcohol dependence.
A sample of 471 alcohol-dependent subjects [363 European Americans (EAs) and 108 African Americans (AAs)] and 235 control subjects (192 EAs and 43 AAs) were included in the analyses. Alcohol dependence diagnoses were made using a structured interview. DNA isolated from whole blood was PCR-amplified, and genotypes were assigned on the basis of agarose gel size fractionation.
Although allele frequencies differed significantly by population, there was no evidence of differences by diagnosis or as a function of any of the three subtypes.
Variable findings in the literature in relation to the association of 5'-HTTLPR alleles to alcohol dependence seem to be due to factors other than the composition of study samples in terms of univariate typologies based on sex, comorbid drug dependence, or age of onset of alcohol dependence.
对酒精成瘾者中血清素转运蛋白(基因座SLC6A4)编码基因启动子区域(5'-HTTLPR)中一个据报道具有功能的多态性进行的关联研究得出了相互矛盾的结果。5'-HTTLPR多态性最常观察到的等位基因是短变体和长变体;与长变体相比,短变体与SLC6A4基因较低的转录活性相关。为了减少可能混淆酒精依赖关联研究的异质性,我们根据性别、合并药物依赖或酒精依赖发病年龄,研究了5'-HTTLPR等位基因与三种二分法酒精成瘾类型的关联。
分析纳入了471名酒精依赖受试者样本[363名欧洲裔美国人(EA)和108名非裔美国人(AA)]以及235名对照受试者(192名EA和43名AA)。使用结构化访谈进行酒精依赖诊断。从全血中分离的DNA进行PCR扩增,并根据琼脂糖凝胶大小分级确定基因型。
虽然等位基因频率在不同人群中存在显著差异,但没有证据表明在诊断方面或作为三种亚型中任何一种的函数存在差异。
文献中关于5'-HTTLPR等位基因与酒精依赖关联的不同结果似乎是由于除了基于性别、合并药物依赖或酒精依赖发病年龄的单变量类型学研究样本组成之外的其他因素。