| Literature DB >> 26958455 |
Benjamin A Tabak1, Suzanne Vrshek-Schallhorn2, Richard E Zinbarg3, Jason M Prenoveau4, Susan Mineka2, Eva E Redei5, Emma K Adam6, Michelle G Craske1.
Abstract
Variation in the CD38 gene, which regulates secretion of the neuropeptide oxytocin, has been associated with several social phenotypes. Specifically, rs3796863 A allele carriers have demonstrated increased social sensitivity. In 400 older adolescents, we used trait-state-occasion modeling to investigate how rs3796863 genotype, baseline ratings of chronic interpersonal stress, and their gene-environment (GxE) interaction predicted trait social anxiety and depression symptoms over six years. We found significant GxE effects for CD38 A-carrier genotypes and chronic interpersonal stress at baseline predicting greater social anxiety and depression symptoms. A significant GxE effect of smaller magnitude was also found for C/C genotype and chronic interpersonal stress predicting greater depression; however, this effect was small compared to the main effect of chronic interpersonal stress. Thus, in the context of chronic interpersonal stress, heightened social sensitivity associated with the rs3796863 A allele may prospectively predict risk for social anxiety and (to a lesser extent) depression.Entities:
Keywords: CD38; depression; gene-environment interaction; interpersonal stress; oxytocin; social anxiety; trait-state-occasion modeling
Year: 2015 PMID: 26958455 PMCID: PMC4779340 DOI: 10.1177/2167702615577470
Source DB: PubMed Journal: Clin Psychol Sci ISSN: 2167-7034