Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States of America.
Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States of America.
PLoS One. 2022 Apr 8;17(4):e0266384. doi: 10.1371/journal.pone.0266384. eCollection 2022.
This study examined whether polygenic risk scores (PRS) for lifetime cannabis and alcohol use were associated with misusing opioids, and whether sex differences existed in these relations in an urban, African-American sample.
Data were drawn from three cohorts of participants (N = 1,103; 45% male) who were recruited in first grade as part of a series of elementary school-based, universal preventive intervention trials conducted in a Mid-Atlantic region of the U.S. In young adulthood, participants provided a DNA sample and reported on whether they had used heroin or misused prescription opioids in their lifetime. Three substance use PRS were computed based on prior GWAS: lifetime cannabis use from Pasman et al. (2018), heavy drinking indexed via maximum number of drinks from Gelernter et al. (2019), and alcohol consumption from Kranzler et al. (2019).
Higher PRS for lifetime cannabis use, greater heavy drinking, and greater alcohol consumption were associated with heightened risk for misusing opioids among the whole sample. Significant sex by PRS interactions were also observed such that higher PRS for heavy drinking and alcohol consumption were associated with a greater likelihood of opioid misuse among males, but not females.
Our findings further elucidate the genetic contributions to misusing opioids by showing that the genetics of cannabis and alcohol consumption are associated with lifetime opioid misuse among young adults, though replication of our findings is needed.
本研究旨在探讨终生大麻和酒精使用的多基因风险评分(PRS)是否与滥用阿片类药物有关,以及在一个城市的非裔美国人群体中,这些关系是否存在性别差异。
数据来自三个队列的参与者(N=1103;45%为男性),他们在一年级时作为一系列在美国中大西洋地区进行的基于小学的普遍性预防干预试验的一部分被招募。在成年早期,参与者提供了一份 DNA 样本,并报告他们一生中是否使用过海洛因或滥用处方类阿片。基于先前的 GWAS,计算了三种物质使用 PRS:帕斯曼等人(2018 年)的终生大麻使用、格尔纳特等人(2019 年)的最大饮酒量指数化的重度饮酒,以及克拉泽勒等人(2019 年)的酒精消费。
在整个样本中,终生大麻使用的 PRS 较高、重度饮酒较多和酒精消费较多与滥用阿片类药物的风险增加有关。还观察到 PRS 与性别之间的显著相互作用,即较高的重度饮酒和酒精消费 PRS 与男性滥用阿片类药物的可能性增加有关,但与女性无关。
我们的发现进一步阐明了滥用阿片类药物的遗传贡献,表明大麻和酒精消费的遗传学与年轻人的终生阿片类药物滥用有关,但需要对我们的发现进行复制。