D'Addario Claudio, Shchetynsky Klementy, Pucci Mariangela, Cifani Carlo, Gunnar Agneta, Vukojević Vladana, Padyukov Leonid, Terenius Lars
Karolinska Institutet, Department of Clinical Neuroscience, Center for Molecular Medicine, Stockholm, Sweden; Faculty of Bioscience and Technology for Food, Agriculture and Environment, University of Teramo, Italy.
Rheumatology Unit, Department of Medicine, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden.
Prog Neuropsychopharmacol Biol Psychiatry. 2017 Jun 2;76:195-203. doi: 10.1016/j.pnpbp.2017.03.012. Epub 2017 Mar 21.
Dynorphins are critically involved in the development, maintenance and relapse of alcoholism. Alcohol-induced changes in the prodynorphin gene expression may be influenced by both gene polymorphisms and epigenetic modifications. The present study of human alcoholics aims to evaluate DNA methylation patterns in the prodynorphin gene (PDYN) promoter and to identify single nucleotide polymorphisms (SNPs) associated with alcohol dependence and with altered DNA methylation. Genomic DNA was isolated from peripheral blood cells of alcoholics and healthy controls, and DNA methylation was studied in the PDYN promoter by bisulfite pyrosequencing. In alcoholics, DNA methylation increased in three of the seven CpG sites investigated, as well as in the average of the seven CpG sites. Data stratification showed lower increase in DNA methylation levels in individuals reporting craving and with higher levels of alcohol consumption. Association with alcoholism was observed for rs2235751 and the presence of the minor allele G was associated with reduced DNA methylation at PDYN promoter in females and younger subjects. Genetic and epigenetic factors within PDYN are related to risk for alcoholism, providing further evidence of its involvement on ethanol effects. These results might be of relevance for developing new biomarkers to predict disease trajectories and therapeutic outcome.
强啡肽在酒精中毒的发生、维持和复发中起关键作用。酒精诱导的前强啡肽基因表达变化可能受基因多态性和表观遗传修饰的影响。本研究针对人类酒精中毒者,旨在评估前强啡肽基因(PDYN)启动子中的DNA甲基化模式,并鉴定与酒精依赖及DNA甲基化改变相关的单核苷酸多态性(SNP)。从酒精中毒者和健康对照者的外周血细胞中分离基因组DNA,采用亚硫酸氢盐焦磷酸测序法研究PDYN启动子中的DNA甲基化。在酒精中毒者中,所研究的7个CpG位点中的3个以及7个CpG位点的平均值处的DNA甲基化增加。数据分层显示,报告有酒瘾且饮酒量较高的个体,其DNA甲基化水平升高幅度较小。观察到rs2235751与酒精中毒有关,且小等位基因G的存在与女性和年轻受试者PDYN启动子处DNA甲基化减少有关。PDYN内的遗传和表观遗传因素与酒精中毒风险相关,为其参与乙醇效应提供了进一步证据。这些结果可能与开发预测疾病轨迹和治疗结果的新生物标志物相关。