VA Medical Center, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
Department of Psychiatry and Behavioral Sciences, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
Alcohol Clin Exp Res. 2019 Jul;43(7):1519-1527. doi: 10.1111/acer.14079. Epub 2019 May 31.
Risk for alcoholism may be enhanced by exposure to early-life adversity (ELA) in persons with genetic vulnerabilities. We examined ELA in the presence of a common variant of the gene for the enzyme catechol-O-methyltransferase (COMT, Val158Met, rs4680) in relation to cortisol reactivity, the onset of early drinking, and experimentation with drugs.
Saliva cortisol reactivity to speech and mental arithmetic stress was measured in 480 healthy young adults (23.5 years of age, 50% females) who experienced either 0, 1, or ≥ 2 forms of ELA during childhood and adolescence, provided information on use of alcohol and recreational drugs, and were genotyped for the Val158Met polymorphism.
ELA led to progressively smaller cortisol responses in the Met/Met and Val/Met allele groups but to progressively larger responses in Val homozygotes, F = 3.29, p = 0.011. ELA independently predicted earlier age at first drink, F = 14.2, p < 0.0001, with a larger effect in Met-allele carriers, F = 13.95, p < 0.00001, and a smaller effect in Val homozygotes, F = 4.14, p = 0.02. Similar effects were seen in recreational drug use. Cortisol reactivity was unrelated to drinking behavior or drug experimentation.
ELA leads to blunted stress reactivity and, independently, contributes to potentially risky drinking and drug-use behaviors in persons carrying 1 or 2 copies of the COMT 158Met allele. The results reinforce the impact of early experience on the stress axis and on risky behaviors, and they point to the 158Met allele as conveying a vulnerability to the early environment.
具有遗传易感性的个体如果在生命早期经历逆境(ELA),则可能会增加患酒精中毒的风险。我们研究了在存在儿茶酚-O-甲基转移酶(COMT,Val158Met,rs4680)基因常见变异的情况下,ELA 与皮质醇反应、早期饮酒开始和药物使用实验之间的关系。
在 480 名健康的年轻成年人(23.5 岁,50%为女性)中测量了唾液皮质醇对演讲和心算应激的反应,这些成年人在儿童和青少年时期经历了 0、1 或≥2 种 ELA,提供了关于使用酒精和娱乐性药物的信息,并对 Val158Met 多态性进行了基因分型。
ELA 导致 Met/Met 和 Val/Met 等位基因组的皮质醇反应逐渐减小,但 Val 纯合子的反应逐渐增大,F=3.29,p=0.011。ELA 独立预测首次饮酒年龄较早,F=14.2,p<0.0001,Met 等位基因携带者的影响更大,F=13.95,p<0.00001,Val 纯合子的影响更小,F=4.14,p=0.02。在娱乐性药物使用中也观察到类似的效果。皮质醇反应与饮酒行为或药物实验无关。
ELA 导致应激反应迟钝,并且独立地导致携带 1 或 2 个 COMT 158Met 等位基因的个体出现潜在危险的饮酒和药物使用行为。结果强化了早期经验对压力轴和危险行为的影响,并指出 158Met 等位基因易受早期环境的影响。