跨越青春期和成年早期的狂饮轨迹:与双系统冲动型人格特征、酒精消费和酒精使用障碍的遗传影响有关。

Alex P Miller, Kellyn M Spychala, Wendy S Slutske, Kim Fromme, Ian R Gizer
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引用次数: 0

摘要

酗酒是青少年中比较常见的一种饮酒模式,其正常频率轨迹在青春期和成年早期达到顶峰。频繁暴饮不仅是导致酒精使用障碍(AUD)的重要风险因素,也会增加酒精相关伤害和死亡的几率,因此是一个重大的公共卫生问题。暴饮在整个成长过程中的变化与冲动型人格特质(IPTs)的变化密切相关,而冲动型人格特质被假定为与大量饮酒和 AUD 遗传风险相关的中间表型。本研究试图探讨在青春期和成年早期,暴饮和醉酒频率的纵向变化在多大程度上与双系统IPTs(即自上而下[缺乏自我控制]和自下而上[寻求感觉和紧迫感])的遗传影响以及酒精消费和AUD的遗传风险相关。在三个独立的纵向样本(N = 10,554)中,使用条件潜增长曲线多基因评分(PGS)模型对相关性进行了测试。结果表明,在所有样本中,寻求感觉的 PGS 与模型截距(即在第一次测量时暴饮暴食的频率较高)和酒精消费的 PGS 与模型斜率(即向暴饮暴食频率峰值陡增)之间存在一致的显著和独立的关联。紧迫性 PGS 与暴饮或醉酒频率的变化无明显关联。总之,这些研究结果强调了独特但相关的IPT和酒精特异性遗传因素在青少年和成年早期暴饮出现和升级中的作用。
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Binge drinking trajectories across adolescence and early adulthood: Associations with genetic influences for dual-systems impulsive personality traits, alcohol consumption, and alcohol use disorder.

Binge drinking is a relatively common pattern of alcohol use among youth with normative frequency trajectories peaking in emerging and early adulthood. Frequent binge drinking is a critical risk factor for not only the development of alcohol use disorders (AUDs) but also increased odds of alcohol-related injury and death, and thus constitutes a significant public health concern. Changes in binge drinking across development are strongly associated with changes in impulsive personality traits (IPTs) which have been hypothesized as intermediate phenotypes associated with genetic risk for heavy alcohol use and AUD. The current study sought to examine the extent to which longitudinal changes in binge drinking and intoxication frequency across adolescence and early adulthood are associated with genetic influences underlying dual-systems IPTs (i.e., top-down [lack of self-control] and bottom-up [sensation seeking and urgency] constructs) alongside genetic risk for alcohol consumption and AUD. Associations were tested using conditional latent growth curve polygenic score (PGS) models in three independent longitudinal samples (N=10,554). Results suggested consistent significant and independent associations across all samples between sensation seeking PGSs and model intercepts (i.e., higher frequency of binge drinking at first measurement occasion) and alcohol consumption PGSs and model slopes (i.e., steeper increases toward peak binge drinking frequency). Urgency PGSs were not significantly associated with changes in binge drinking or intoxication frequency. Collectively, these findings highlight the role of unique but correlated IPT and alcohol-specific genetic factors in the emergence and escalation of binge drinking during adolescence and early adulthood.

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