The sample includes 349 participants (59% female, 96% White) who were assessed at five points between mean ages 16 and 33. At each assessment, participants reported on their own alcohol use and the proportion of close friends who used alcohol (in adolescence) or drank heavily (in adulthood). Genotyping of DRD4 polymorphism was conducted from saliva samples. Multiple regressions predicted alcohol use at subsequent time points from friends’ alcohol use, DRD4 (dichotomized as low vs. high risk), and their interaction, adjusting for alcohol use at baseline, sex, ethnicity, and family income.
Having the long allele of DRD4 interacted with friends’ drinking in adulthood (ages 24 and 29), but not in adolescence (ages 16 and 17). Specifically, friends’ alcohol use in adolescence predicted subsequent drinking regardless of DRD4 genotype. However, friends’ drinking in adulthood was associated with later increased heavy drinking only among participants with the long allele of the DRD4, and not among those without this genetic risk. This pattern of results replicated across multiple measures of alcohol use and alcohol problems.
The results provide strong evidence that the long allele of DRD4 increases individuals’ susceptibility to friends’ heavy alcohol use in adulthood, but not in adolescence. The findings are consistent with behavior genetic studies reporting strong environmental influences on adolescent drinking, with the role of genetic factors increasing in adulthood (Kendler et al., 2008). Adults with the long allele of DRD4 may benefit from interventions designed to help them reduce affiliations with heavy drinking friends or decrease these peer influences. Additional genetic markers are currently being genotyped and will be included in the presentation.