Department of Psychiatry, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Behav Brain Funct. 2012 Jul 11;8:18. doi: 10.1186/1744-9081-8-18.
Several studies have hypothesized that genes regulating the components of the serotonin system, including serotonin transporter (5-HTTLPR) and serotonin 1 B receptor (5-HT1B), may be associated with alcoholism, but their results are contradictory because of alcoholism's heterogeneity. Therefore, we examined whether the 5-HTTLPR gene and 5-HT1B gene G861C polymorphism are susceptibility factors for a specific subtype of alcoholism, antisocial alcoholism in Han Chinese in Taiwan.
We recruited 273 Han Chinese male inmates with antisocial personality disorder (ASPD) [antisocial alcoholism (AS-ALC) group (n=120) and antisocial non-alcoholism (AS-N-ALC) group (n=153)] and 191 healthy male controls from the community. Genotyping was done using PCR-RFLP.
There were no significant differences in the genotypic frequency of the 5-HT1B G861C polymorphism between the 3 groups. Although AS-ALC group members more frequently carried the 5-HTTLPR S/S, S/LG, and LG/LG genotypes than controls, the difference became non-significant after controlling for the covarying effects of age. However, the 5-HTTLPR S/S, S/LG, and LG/LG genotypes may have interacted with the 5-HT1B G861C C/C polymorphism and increased the risk of becoming antisocial alcoholism.
Our study suggests that neither the 5-HTTLPR gene nor the 5-HT1B G861C polymorphism alone is a risk factor for antisocial alcoholism in Taiwan's Han Chinese population, but that the interaction between both genes may increase susceptibility to antisocial alcoholism.
有几项研究假设,调节 5-羟色胺系统成分的基因,包括 5-羟色胺转运体(5-HTTLPR)和 5-羟色胺 1B 受体(5-HT1B),可能与酗酒有关,但由于酗酒的异质性,它们的结果相互矛盾。因此,我们研究了 5-HTTLPR 基因和 5-HT1B 基因 G861C 多态性是否是台湾汉族人群特定酗酒亚型(反社会酗酒)的易感因素。
我们招募了 273 名汉族男性囚犯,他们患有反社会人格障碍(ASPD)[反社会酗酒(AS-ALC)组(n=120)和反社会非酗酒(AS-N-ALC)组(n=153)]和 191 名来自社区的健康男性对照。采用 PCR-RFLP 法进行基因分型。
3 组间 5-HT1B G861C 多态性的基因型频率无显著差异。尽管 AS-ALC 组成员比对照组更频繁携带 5-HTTLPR S/S、S/LG 和 LG/LG 基因型,但在控制年龄的协变量影响后,差异变得无统计学意义。然而,5-HTTLPR S/S、S/LG 和 LG/LG 基因型可能与 5-HT1B G861C C/C 多态性相互作用,增加了患反社会酗酒的风险。
本研究表明,5-HTTLPR 基因或 5-HT1B G861C 多态性单独均不是台湾汉族人群反社会酗酒的危险因素,但两者的相互作用可能会增加反社会酗酒的易感性。