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Genomic influences on alcohol problems in a population‐based sample of young adults
Author(s) -
Edwards Alexis C.,
Aliev Fazil,
Wolen Aaron R.,
Salvatore Jessica E.,
Gardner Charles O.,
McMahon George,
Evans David M.,
Macleod John,
Hickman Matthew,
Dick Danielle M.,
Kendler Kenneth S.
Publication year - 2015
Publication title -
addiction
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.424
H-Index - 193
eISSN - 1360-0443
pISSN - 0965-2140
DOI - 10.1111/add.12822
Subject(s) - alcohol , sample (material) , population , young adult , genetics , psychology , medicine , clinical psychology , psychiatry , biology , environmental health , developmental psychology , chemistry , chromatography , biochemistry
Aims Alcohol problems (AP) contribute substantially to the global disease burden. Twin and family studies suggest that AP are genetically influenced, although few studies have identified variants or genes that are robustly associated with risk. This study identifies genetic and genomic influences on AP during young adulthood, which is often when drinking habits are established. Design We conducted a genome‐wide association study of AP. We further conducted gene‐based tests, gene ontology analyses and functional genomic enrichment analyses to assess genomic factors beyond single variants that are relevant to AP. Setting The Avon Longitudinal Study of Parents and Children, a large population‐based study of a UK birth cohort. Participants Genetic and phenotypical data were available for 4304 participants. Measurements The AP phenotype was a factor score derived from items from the Alcohol Use Disorders Identification Test, symptoms of DSM‐IV alcohol dependence, and three additional problem‐related items. Findings One variant met genome‐wide significance criteria. Four out of 22 880 genes subjected to gene‐based analyses survived a stringent significance threshold ( q < 0.05); none of these have been implicated previously in alcohol‐related phenotypes. Several biologically plausible gene ontologies were statistically over‐represented among implicated single nucleotide polymorphisms (SNPs). SNPs on the Illumina 550 K SNP chip accounted for ~5% of the phenotypical variance in AP. Conclusions Genetic and genomic factors appear to play a role in alcohol problems in young adults. Genes involved in nervous system‐related processes, such as signal transduction and neurogenesis, potentially contribute to liability to alcohol problems, as do genes expressed in non‐brain tissues.