Department of Sociology, University of Kentucky, 1515 Patterson Office Tower, Lexington, KY 40506-0027, USA.
Behav Genet. 2013 Sep;43(5):402-14. doi: 10.1007/s10519-013-9607-9. Epub 2013 Aug 23.
Gender-moderated gene-environment interactions are rarely explored, raising concerns about inaccurate specification of etiological models and inferential errors. The current study examined the influence of gender, negative and positive daily life events, and GABRA2 genotype (SNP rs279871) on alcohol dependence, testing two- and three-way interactions between these variables using multi-level regression models fit to data from 2,281 White participants in the Collaborative Study on the Genetics of Alcoholism. Significant direct effects of variables of interest were identified, as well as gender-specific moderation of genetic risk on this SNP by social experiences. Higher levels of positive life events were protective for men with the high-risk genotype, but not among men with the low-risk genotype or women, regardless of genotype. Our findings support the disinhibition theory of alcohol dependence, suggesting that gender differences in social norms, constraints and opportunities, and behavioral undercontrol may explain men and women's distinct patterns of association.
性别调节的基因-环境相互作用很少被探索,这引起了人们对病因模型不准确指定和推理错误的担忧。本研究考察了性别、负面和正面的日常生活事件以及 GABRA2 基因型(SNP rs279871)对酒精依赖的影响,使用多水平回归模型检验了这些变量之间的二项和三项交互作用,这些数据来自于酒精遗传学合作研究中 2281 名白种人参与者。确定了感兴趣变量的显著直接效应,以及由社会经验引起的该 SNP 上遗传风险的性别特异性调节。高水平的积极生活事件对高风险基因型的男性具有保护作用,但对低风险基因型的男性或女性没有保护作用,无论基因型如何。我们的研究结果支持酒精依赖的去抑制理论,表明社会规范、约束和机会以及行为失控方面的性别差异可能解释了男性和女性之间不同的关联模式。