Chung Patrick, Logge Warren B, Riordan Benjamin C, Haber Paul S, Merriman Marilyn E, Phipps-Green Amanda, Topless Ruth K, Merriman Tony R, Conner Tamlin, Morley Kirsten C
Discipline of Addiction Medicine, Central Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
Psychological Medicine, Central Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
Front Psychiatry. 2020 Dec 7;11:549429. doi: 10.3389/fpsyt.2020.549429. eCollection 2020.
Risk behaviors for young adults such as alcohol use are associated with increased risk of morbidity and mortality. Patterns of risk behavior may be genetically determined and vary between genders. Previous studies in both young adults and heavy drinking adult samples have demonstrated that some genotypes, such as A118G, Val158Met and Taq1A and C52IT, may predict addictive behaviors including alcohol consumption and impulsivity, although results have been mixed. This study aimed to investigate the predictive relationship of these four single nucleotide polymorphisms (SNPs) prospectively on student patterns of drinking using a micro-longitudinal daily diary design in a sample of 628 young adults ages 18-25 of predominantly of European ethnicity. Linear mixed models were used to examine the effect of SNPs on the number of drinks per drinking session with gender as a moderating variable. There were no main effects for genotype on alcohol consumption, nor for gender × genotype for any of the SNPs. There was a trend for an effect of the Taq1A on the number of drinks per drinking day and for the interaction of gender and Taq1A on the number of drinks per drinking day. These findings suggest that the Taq1A A118G, C521T, or Val158Met polymorphisms, are not associated with alcohol consumption in young adults, although there may be a relationship between Taq1A and alcohol consumption in young adult males.
诸如饮酒等年轻人的风险行为与发病率和死亡率增加相关。风险行为模式可能由基因决定,且存在性别差异。此前针对年轻人和大量饮酒成年人样本的研究表明,某些基因型,如A118G、Val158Met、Taq1A和C52IT,可能预测包括饮酒和冲动性在内的成瘾行为,尽管结果不一。本研究旨在采用微观纵向每日日记设计,对628名年龄在18 - 25岁、主要为欧洲裔的年轻人样本,前瞻性地研究这四种单核苷酸多态性(SNP)与学生饮酒模式之间的预测关系。使用线性混合模型,以性别作为调节变量,检验SNP对每次饮酒的饮酒量的影响。基因型对酒精消费没有主效应,任何SNP的性别×基因型交互作用也没有主效应。Taq1A对每日饮酒量有影响趋势,且性别与Taq1A对每日饮酒量存在交互作用。这些发现表明,Taq1A A118G、C521T或Val158Met多态性与年轻人的酒精消费无关,尽管Taq1A与年轻成年男性的酒精消费之间可能存在关系。