Department of Psychology, Boston University, Boston, MA 02215, USA.
Drug Alcohol Depend. 2010 Apr 1;108(1-2):1-6. doi: 10.1016/j.drugalcdep.2009.11.017. Epub 2010 Jan 8.
Previous studies have implicated a relationship between particular allelic variations of the serotonin transporter gene (5HTTLPR) and alcohol dependence. To provide a current estimate of the strength of this association, particularly in light of inconsistent results for 5HTTLPR, we conducted a meta-analytic review of the association between 5HTTLPR and a clinical diagnosis of alcohol dependence. Of 145 studies initially identified, 22 (including 8050 participants) met inclusion criteria. Results indicated that there was a significant albeit modest association between alcohol dependence diagnosis and the presence of at least 1 short allele (OR=1.15, 95% CI=1.01, 1.30, p<.05). Slightly more robust results were observed for participants who were homogeneous for the short allele (OR=1.21, 95% CI=1.02, 1.44, p<.05). These results were unrelated to sex and race/ethnicity of participants; however, the effect size was moderated by study sample size and publication year. Additionally, the fail-safe N analysis indicated potential publication bias. Therefore, although our review indicates that there is a significant association between 5HTTLPR and alcohol dependence diagnosis, this result should be interpreted with caution.
先前的研究表明,5-羟色胺转运体基因(5HTTLPR)的特定等位基因变异与酒精依赖之间存在关联。为了提供对这种关联强度的最新估计,特别是考虑到 5HTTLPR 的结果不一致,我们对 5HTTLPR 与酒精依赖临床诊断之间的关联进行了荟萃分析综述。在最初确定的 145 项研究中,有 22 项(包括 8050 名参与者)符合纳入标准。结果表明,酒精依赖诊断与至少存在 1 个短等位基因之间存在显著但适度的关联(OR=1.15,95% CI=1.01,1.30,p<.05)。对于短等位基因同质的参与者,观察到的结果略为稳健(OR=1.21,95% CI=1.02,1.44,p<.05)。这些结果与参与者的性别和种族/民族无关;然而,研究样本量和发表年份调节了效应大小。此外,失效安全 N 分析表明存在潜在的发表偏倚。因此,尽管我们的综述表明 5HTTLPR 与酒精依赖诊断之间存在显著关联,但应谨慎解释这一结果。