SooHoo Jackson F, Davis Christal N, Han Angela, Jinwala Zeal, Gelernter Joel, Feinn Richard, Kranzler Henry R
Center for Studies of Addiction, Department of Psychiatry, University of Pennsylvania School of Medicine, Philadelphia, PA, USA.
Mental Illness Research, Education, and Clinical Center, Crescenz VAMC, Philadelphia, PA, USA.
Psychol Med. 2025 May 2;55:e132. doi: 10.1017/S0033291725001163.
Genetic and environmental factors, including adverse childhood experiences (ACEs), contribute to substance use disorders (SUDs). However, the interactions between these factors are poorly understood.
We examined associations between SUD polygenic scores (PGSs), ACEs, and the initiation of use and severity of alcohol (AUD), opioid use disorder (OUD), and cannabis use disorder (CanUD) in 10,275 individuals (43.5% female, 47.2% African-like ancestry [AFR], and 52.8% European-like ancestry [EUR]). ACEs and SUD severity were modeled as latent factors. We conducted logistic and linear regressions within ancestry groups to examine the associations of ACEs, PGS, and their interaction with substance use initiation and SUD severity.
All three SUD PGS were associated with ACEs in EUR individuals, indicating a gene-environment correlation. Among EUR individuals, only the CanUD PGS was associated with initiating use, whereas ACEs were associated with initiating use of all three substances in both ancestry groups. Additionally, a negative gene-by-environment interaction was identified for opioid initiation in EUR individuals. ACEs were associated with all three SUD severity latent factors in EUR individuals and with AUD and CanUD severity in AFR individuals. PGS were associated with AUD severity in both ancestry groups and with CanUD severity in AFR individuals. Gene-by-environment interactions were identified for AUD and CanUD severity among EUR individuals.
Findings highlight the roles of ACEs and polygenic risk in substance use initiation and SUD severity. Gene-by-environment interactions implicate ACEs as moderators of genetic susceptibility, reinforcing the importance of considering both genetic and environmental influences on SUD risk.
包括童年不良经历(ACEs)在内的遗传和环境因素会导致物质使用障碍(SUDs)。然而,这些因素之间的相互作用却知之甚少。
我们在10275名个体(43.5%为女性,47.2%为非洲裔血统[AFR],52.8%为欧洲裔血统[EUR])中,研究了SUD多基因评分(PGSs)、ACEs与酒精使用障碍(AUD)、阿片类物质使用障碍(OUD)和大麻使用障碍(CanUD)的使用起始及严重程度之间的关联。ACEs和SUD严重程度被建模为潜在因素。我们在不同血统组内进行逻辑回归和线性回归,以研究ACEs、PGS及其相互作用与物质使用起始和SUD严重程度之间的关联。
在欧洲裔个体中,所有三种SUD PGS均与ACEs相关,表明存在基因-环境相关性。在欧洲裔个体中,只有CanUD PGS与使用起始相关,而在两个血统组中,ACEs均与所有三种物质的使用起始相关。此外,在欧洲裔个体中,发现阿片类物质使用起始存在负向基因-环境相互作用。在欧洲裔个体中,ACEs与所有三种SUD严重程度潜在因素相关,在非洲裔个体中与AUD和CanUD严重程度相关。PGS在两个血统组中均与AUD严重程度相关,在非洲裔个体中与CanUD严重程度相关。在欧洲裔个体中,发现AUD和CanUD严重程度存在基因-环境相互作用。
研究结果突出了ACEs和多基因风险在物质使用起始和SUD严重程度中的作用。基因-环境相互作用表明ACEs是遗传易感性的调节因子,强化了考虑遗传和环境对SUD风险影响的重要性。