Examining interactions between polygenic scores and interpersonal trauma exposure on alcohol consumption and use disorder in an ancestrally diverse college cohort

Front Genet. 2024 Feb 1:14:1274381. doi: 10.3389/fgene.2023.1274381. eCollection 2023.

Abstract

Introduction: Genetic factors impact alcohol consumption and use disorder (AUD), with large-scale genome-wide association studies (GWAS) identifying numerous associated variants. Aggregate genetic methods in combination with important environmental factors (e.g., interpersonal trauma [IPT]) can be applied to expand our understanding of the ways by which genetic and environmental variables work together to influence alcohol consumption and disordered use. The present study aimed to detail the relationships between genome-wide polygenic scores (PGS) for alcohol phenotypes (i.e., alcohol consumption and AUD status) and IPT exposure as well as the interaction between them across ancestry. Methods: Data were drawn from the Spit for Science (S4S) study, a US college student population, where participants reported on IPT exposure prior to college and alcohol consumption and problems during college (N = 9,006; ancestry: 21.3% African [AFR], 12.5% Admixed Americas [AMR], 9.6% East Asian [EAS], 48.1% European [EUR], 8.6% South Asian [SAS]). Two trans-ancestry PGS were constructed, one for alcohol consumption and another for AUD, using large-scale GWAS summary statistics from multiple ancestries weighted using PRS-CSx. Regression models were applied to test for the presence of associations between alcohol-PGS and IPT main and interaction effects. Results: In the meta-analysis across ancestry groups, IPT exposure and PGS were significantly associated with alcohol consumption (βIPT = 0.31, P IPT = 0.0002; βPGS = 0.09, P PGS = 0.004) and AUD (ORIPT = 1.12, P IPT = 3.5 × 10-8; ORPGS = 1.02, P PGS = 0.002). No statistically significant interactions were detected between IPT and sex nor between IPT and PGS. When inspecting ancestry specific results, the alcohol consumption-PGS and AUD-PGS were only statistically significant in the EUR ancestry group (βPGS = 0.09, P PGS = 0.04; ORPGS = 1.02, P PGS = 0.022, respectively). Discussion: IPT exposure prior to college was strongly associated with alcohol outcomes in this college-age sample, which could be used as a preventative measure to identify students at high risk for problematic alcohol use. Additionally, results add to developing evidence of polygenic score association in meta-analyzed samples, highlighting the importance of continued efforts to increase ancestral representation in genetic studies and inclusive analytic approaches to increase the generalizability of results from genetic association studies.

Keywords: alcohol consumption; alcohol use disorder (AUD); college and university students; interpersonal trauma; physical assault; polygenic score (PGS); sexual assault; trans-ancestry.

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported in part by the National Institutes of Health (NIH) including the National Institute on Alcohol Abuse and Alcoholism (NIAAA) K01AA025692 (CMS), P50AA022537 (REP); National Institute on General Medical Sciences (NIGMS) 5K12GM093857-11 (EEL); National Institute of Drug Abuse (NIDA) R01DA054313 (EPW); National Institute of Mental Health (NIMH) R01MH125938 (REP, EEL, CC); 5R25DA051339-03 (HSR). This work was also supported by the Virginia Commonwealth University (VCU) Institute for Research on Behavioral and Emotional Health (IRBEH; REP, CMS, RO, EPW, EEL). Spit for Science has been supported by VCU, P20AA017828, R37AA011408, K02AA018755, P50AA022537, and K01AA024152 from NIAAA and UL1RR031990 from the National Center for Research Resources and NIH Roadmap for Medical Research, as well as support by the Center for the Study of Tobacco Products at VCU. REDCap support is provided by CTSA award UM1TR004360 from the National Center for Advancing Translational Sciences. The content is solely the responsibility of the authors and does not necessarily represent the views of the respective funding agencies.