MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK; Department of Population Health Sciences, Bristol Medical School, University of Bristol, UK.
MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK; Department of Population Health Sciences, Bristol Medical School, University of Bristol, UK.
Drug Alcohol Depend. 2021 Apr 1;221:108654. doi: 10.1016/j.drugalcdep.2021.108654. Epub 2021 Feb 27.
Heavy alcohol consumption often co-occurs with mental health problems; this could be due to confounding, shared biological mechanisms, or causal effects. Polygenic risk scores (PRS) for alcohol use can be used to explore this association at critical life stages.
We characterized a PRS reliably associated with patterns of adult alcohol consumption by 1) validating whether it predicts own alcohol use at different life-stages (pregnancy, adolescence) of interest for mental health impact. Additionally, we explored associations of alcohol PRS on mental health phenotypes 2) within-individuals (using own alcohol PRS on own phenotypes) and 3) intergenerationally (using maternal alcohol PRS on offspring phenotypes). We used data from the Avon Longitudinal Study of Parents and Children (ALSPAC) (n = 960-7841). Additional substance abuse behaviors and mental health/behavioral outcomes were investigated (alcohol phenotypes n = 22; health phenotypes n = 91).
Maternal alcohol PRS was associated with consumption during pregnancy (strongest signal: alcohol frequency at 18 weeks' gestation: β = 0.041, 95%CI = 0.0.02-0.06), p = 1.01 × 10, adjusted R = 1.6 %), offspring alcohol PRS did not predict offspring alcohol consumption. We found evidence for an association of maternal alcohol PRS with own perinatal depression (OR = 1.10, 95% CI = 1.02 to 1.18, p = 0.022) and decreased offspring intellectual ability (β=-0.209, 95% CI -0.38 to -0.04, p= 0.016).
These alcohol PRS are a valid proxy for maternal alcohol use in pregnancy. Offspring alcohol PRS was not associated with drinking in adolescence. Consistently with results from different study designs, we found evidence that maternal alcohol PRS are associated with both prenatal depression and decreased offspring intellectual ability.
大量饮酒常与心理健康问题同时发生;这可能是由于混杂因素、共同的生物学机制或因果效应。用于酒精使用的多基因风险评分(PRS)可用于探索在关键生命阶段的这种关联。
我们通过以下方式来描述与成年饮酒模式可靠相关的 PRS:1)验证其是否可以预测在心理健康有影响的感兴趣的不同生命阶段(妊娠、青春期)的自身饮酒情况。此外,我们还探索了个体内(使用自身的酒精 PRS 来预测自身的表型)和代际间(使用母亲的酒精 PRS 来预测后代的表型)的酒精 PRS 与心理健康表型的关联。我们使用了来自阿冯纵向研究父母和儿童(ALSPAC)的数据(n=960-7841)。还调查了其他物质滥用行为和心理健康/行为结果(酒精表型 n=22;健康表型 n=91)。
母亲的酒精 PRS 与妊娠期间的饮酒量相关(最强信号:18 周妊娠时的酒精频率:β=0.041,95%CI=0.00-0.06,p=1.01×10-4,调整后的 R=1.6%),而后代的酒精 PRS 并不能预测后代的饮酒量。我们发现母亲的酒精 PRS 与自身围产期抑郁(OR=1.10,95%CI=1.02-1.18,p=0.022)和后代智力下降(β=-0.209,95%CI=-0.38 至-0.04,p=0.016)有关联的证据。
这些酒精 PRS 是妊娠期间母亲饮酒的有效替代指标。后代的酒精 PRS 与青春期饮酒无关。与来自不同研究设计的结果一致,我们发现证据表明,母亲的酒精 PRS 与产前抑郁和后代智力下降都有关联。