Mrug Sylvie, Windle Michael
University of Alabama at Birmingham, Department of Psychology, 1720 Second Avenue South, CH415, Birmingham, AL 35294-1170, United States.
Emory University, Department of Behavioral Science and Health Education, 1518 Clifton Road NE, Room 514, Atlanta, GA 30322, United States.
Drug Alcohol Depend. 2014 Dec 1;145:168-73. doi: 10.1016/j.drugalcdep.2014.10.009. Epub 2014 Oct 23.
The long allele of DRD4 is associated with greater susceptibility to peer influences on alcohol use in young adulthood, but it is unclear whether this increased susceptibility extends to other developmental periods. This study examined the interactive effects of DRD4 polymorphism and friends' alcohol use from adolescence to adulthood.
Participants (N = 340; 59% female; 98% White) reported on their own and their friends' alcohol use at four time points between mean ages 17 and 33. Autoregressive cross-lagged models evaluated reciprocal relationships between friends' alcohol use and participants' own alcohol use and frequency of heavy drinking over time. Multigroup modeling tested differences in model paths and covariances across high vs. low risk DRD4 polymorphisms.
Alcohol use at age 33 was predicted by previous friends' alcohol use and correlated with current friends' alcohol use only for carriers of the DRD4 long allele. Regardless of DRD4 genotype, friends' alcohol use at age 17 predicted greater alcohol use and more frequent heavy drinking at age 23. Alcohol use and/or heavy drinking predicted greater friends' alcohol use at later time points for both genotype groups across adolescence and adulthood.
The long allele of DRD4 is associated with increased susceptibility to peer influences on alcohol use in young adulthood, but not earlier in development. Adults with the long allele of DRD4 may benefit from interventions educating them about this risk and equipping them with strategies to reduce affiliations with and influence of drinking friends.
多巴胺D4受体基因(DRD4)的长等位基因与青年期酒精使用受同伴影响的易感性增加有关,但尚不清楚这种增加的易感性是否会延伸到其他发育阶段。本研究考察了DRD4基因多态性与从青少年到成年期朋友饮酒行为之间的交互作用。
参与者(N = 340;59%为女性;98%为白人)在平均年龄17岁至33岁之间的四个时间点报告了自己及朋友的饮酒情况。自回归交叉滞后模型评估了朋友饮酒行为与参与者自身饮酒行为及随时间推移的重度饮酒频率之间的相互关系。多组模型检验了高风险与低风险DRD4基因多态性在模型路径和协方差方面的差异。
只有DRD4长等位基因携带者的33岁时饮酒行为可由之前朋友的饮酒行为预测,且与当前朋友的饮酒行为相关。无论DRD4基因型如何,17岁时朋友的饮酒行为可预测23岁时更多的饮酒行为和更频繁的重度饮酒。在整个青少年期和成年期,两个基因型组的饮酒行为和/或重度饮酒在后期时间点均可预测朋友更多的饮酒行为。
DRD4长等位基因与青年期酒精使用受同伴影响的易感性增加有关,但在发育早期并非如此。携带DRD4长等位基因的成年人可能会从相关干预措施中受益,这些干预措施应让他们了解这种风险,并为他们提供减少与饮酒朋友交往及受其影响的策略。