Citation

Sanchez-Roige S, Fontanillas P, Elson SL, Gray JC, de Wit H, Davis LK, Mackillop J, Palmer AA. Addict. Biol. 2019; 24(1): 121-131.

Affiliation

Institute for Genomic Medicine, University of California San Diego, La Jolla, CA, USA.

Copyright

(Copyright © 2019, John Wiley and Sons)

DOI

10.1111/adb.12574

PMID

29058377

Abstract

Genetic factors contribute to the risk for developing alcohol use disorder (AUD). In collaboration with the genetics company 23andMe, Inc., we performed a genome-wide association study of the alcohol use disorder identification test (AUDIT), an instrument designed to screen for alcohol misuse over the past year. Our final sample consisted of 20 328 research participants of European ancestry (55.3% females; mean age = 53.8, SD = 16.1) who reported ever using alcohol. Our results showed that the 'chip-heritability' of AUDIT score, when treated as a continuous phenotype, was 12%. No loci reached genome-wide significance. The gene ADH1C, which has been previously implicated in AUD, was among our most significant associations (4.4 × 10(-7) ; rs141973904). We also detected a suggestive association on chromosome 1 (2.1 × 10(-7) ; rs182344113) near the gene KCNJ9, which has been implicated in mouse models of high ethanol drinking. Using linkage disequilibrium score regression, we identified positive genetic correlations between AUDIT score, high alcohol consumption and cigarette smoking. We also observed an unexpected positive genetic correlation between AUDIT and educational attainment and additional unexpected negative correlations with body mass index/obesity and attention-deficit/hyperactivity disorder. We conclude that conducting a genetic study using responses to an online questionnaire in a population not ascertained for AUD may represent a cost-effective strategy for elucidating aspects of the etiology of AUD.

© 2017 Society for the Study of Addiction.

Language: en

Keywords

AUDIT; GWAS; alcohol use disorder; alcohol-metabolizing enzymes; complex traits; genetic