Abstract
AbstractAimsThe study aimed to identify specific genes and functional genetic variants affecting susceptibility to two alcohol related phenotypes: heavy drinking and problem drinking.MethodsPhenotypic and exome sequence data was downloaded from the UK Biobank. Reported drinks in the last 24 hours was used to define heavy drinking while responses to a mental health questionnaire defined problem drinking. Gene-wise weighted burden analysis was applied, with genetic variants which were rarer and/or had a more severe functional effect being weighted more highly. Additionally, previously reported variants of interest were analysed inidividually.ResultsOf exome sequenced subjects, for heavy drinking there were 8,166 cases and 84,461 controls while for problem drinking there were 7,811 cases and 59,606 controls. No gene was formally significant after correction for multiple testing but three genes possibly related to autism were significant at p < 0.001,FOXP1, ARHGAP33andCDH9, along withVGFwhich may also be of psychiatric interest. Well established associations with rs1229984 inADH1Band rs671 inALDH2were confirmed but previously reported variants inALDH1B1andGRM3were not associated with either phenotype.ConclusionsThis large study fails to conclusively implicate any novel genes or variants. It is possible that more definitive results will be obtained when sequence data for the remaining UK Biobank participants becomes available and/or if data can be obtained for a more extreme phenotype such as alcohol dependence disorder. This research has been conducted using the UK Biobank Resource.Short summaryTests for association of rare, functional genetic variants with heavy drinking and problem drinking confirm the known effects of variants inADH1BandALDH2but fail to implicate novel variants or genes. Results for three genes potentially related to autism suggest they might exert a protective effect.
Publisher
Cold Spring Harbor Laboratory