Institute for Behavioral Genetics, University of Colorado Boulder, CO.
Department of Psychology and Neuroscience, University of Colorado Boulder, CO.
Sleep. 2021 Mar 12;44(3). doi: 10.1093/sleep/zsaa188.
Estimate the genetic relationship of cannabis use with sleep deficits and an eveningness chronotype.
We used linkage disequilibrium score regression (LDSC) to analyze genetic correlations between sleep deficits and cannabis use behaviors. Secondly, we generated sleep deficit polygenic risk score (PRS) and estimated their ability to predict cannabis use behaviors using linear and logistic regression. Summary statistics came from existing genome-wide association studies of European ancestry that were focused on sleep duration, insomnia, chronotype, lifetime cannabis use, and cannabis use disorder (CUD). A target sample for PRS prediction consisted of high-risk participants and participants from twin/family community-based studies (European ancestry; n = 760, male = 64%; mean age = 26.78 years). Target data consisted of self-reported sleep (sleep duration, feeling tired, and taking naps) and cannabis use behaviors (lifetime ever use, number of lifetime uses, past 180-day use, age of first use, and lifetime CUD symptoms).
Significant genetic correlation between lifetime cannabis use and an eveningness chronotype (rG = 0.24, p < 0.001), as well as between CUD and both short sleep duration (<7 h; rG = 0.23, p = 0.017) and insomnia (rG = 0.20, p = 0.020). Insomnia PRS predicted earlier age of first cannabis use (OR = 0.92, p = 0.036) and increased lifetime CUD symptom count (OR = 1.09, p = 0.012).
Cannabis use is genetically associated with both sleep deficits and an eveningness chronotype, suggesting that there are genes that predispose individuals to both cannabis use and sleep deficits.
估计大麻使用与睡眠不足和夜间型时型的遗传关系。
我们使用连锁不平衡评分回归(LDSC)分析睡眠不足和大麻使用行为之间的遗传相关性。其次,我们生成睡眠不足多基因风险评分(PRS),并使用线性和逻辑回归估计它们预测大麻使用行为的能力。汇总统计数据来自关注睡眠时长、失眠、时型、终生大麻使用和大麻使用障碍(CUD)的欧洲血统全基因组关联研究。PRS 预测的目标样本包括高风险参与者和来自双胞胎/家庭社区研究的参与者(欧洲血统;n=760,男性=64%;平均年龄=26.78 岁)。目标数据包括自我报告的睡眠(睡眠时长、疲倦感和小睡)和大麻使用行为(终生曾使用、使用次数、过去 180 天使用、首次使用年龄和终生 CUD 症状)。
终生大麻使用与夜间型时型之间存在显著的遗传相关性(rG=0.24,p<0.001),以及 CUD 与睡眠时长较短(<7 h;rG=0.23,p=0.017)和失眠(rG=0.20,p=0.020)之间存在显著的遗传相关性。失眠 PRS 预测首次大麻使用年龄较早(OR=0.92,p=0.036)和终生 CUD 症状数增加(OR=1.09,p=0.012)。
大麻使用与睡眠不足和夜间型时型在遗传上相关,这表明存在使个体易患大麻使用和睡眠不足的基因。