Randesi Matthew, van den Brink Wim, Levran Orna, Blanken Peter, Butelman Eduardo R, Yuferov Vadim, da Rosa Joel Correa, Ott Jurg, van Ree Jan M, Kreek Mary Jeanne
Laboratory of the Biology of Addictive Diseases, The Rockefeller University, 1230 York Avenue, New York, NY 10065, USA.
Central Committee on the Treatment of Heroin Addicts (CCBH), Utrecht, The Netherlands; Amsterdam Institute for Addiction Research, Department of Psychiatry, Academic Medical Center, University of Amsterdam, PO Box 22660, 1100 DD, Amsterdam, The Netherlands.
Drug Alcohol Depend. 2016 Nov 1;168:164-169. doi: 10.1016/j.drugalcdep.2016.08.634. Epub 2016 Sep 5.
BACKGROUND: Heroin addiction is a chronic, relapsing brain disease. Genetic factors are involved in the development of drug addiction. The aim of this study was to determine whether specific variants in genes of the opioid system are associated with non-dependent opioid use and heroin dependence. METHODS: Genetic information from four subject groups was collected: non-dependent opioid users (NOD) [n=163]; opioid-dependent (OD) patients in methadone maintenance treatment (MMT) [n=143]; opioid-dependent MMT-resistant patients in heroin-assisted treatment (HAT) [n=138]; and healthy controls with no history of opioid use (HC) [n=153]. Eighty-two variants in eight opioid system genes were studied. To establish the role of these genes in (a) non-dependent opioid use, and (b) heroin dependence, the following groups were compared: HC vs. NOD; HC vs. OD (MMT+HAT); and NOD vs. OD (MMT+HAT). RESULTS: Five unique SNPs in four genes showed nominally significant associations with non-dependent opioid use and heroin dependence. The association of the delta opioid receptor (OPRD1) intronic SNP rs2236861 with non-dependent opioid use (HC vs. NOD) remained significant after correction for multiple testing (OR=0.032; p=0.015). This SNP exhibited a significant gene-gene interaction with prepronociceptin (PNOC) SNP rs2722897 (OR=5.24; p=0.041) (HC vs. NOD). CONCLUSIONS: This study identifies several new and some previously reported associations of variants with heroin dependence and with non-dependent opioid use, an important and difficult to obtain group not extensively studied previously. Further studies are warranted to confirm and elucidate the potential roles of these variants in the vulnerability to illicit drug use and drug addiction.
背景:海洛因成瘾是一种慢性复发性脑部疾病。遗传因素参与药物成瘾的发展过程。本研究的目的是确定阿片系统基因中的特定变体是否与非依赖性阿片类药物使用及海洛因依赖有关。 方法:收集了四组受试者的遗传信息:非依赖性阿片类药物使用者(NOD)[n = 163];接受美沙酮维持治疗(MMT)的阿片类药物依赖(OD)患者[n = 143];接受海洛因辅助治疗(HAT)的阿片类药物依赖且对MMT耐药的患者[n = 138];以及无阿片类药物使用史的健康对照(HC)[n = 153]。对八个阿片系统基因中的82个变体进行了研究。为确定这些基因在(a)非依赖性阿片类药物使用及(b)海洛因依赖中的作用,对以下几组进行了比较:HC与NOD;HC与OD(MMT + HAT);以及NOD与OD(MMT + HAT)。 结果:四个基因中的五个独特单核苷酸多态性(SNP)与非依赖性阿片类药物使用及海洛因依赖呈现出名义上的显著关联。在进行多重检验校正后,δ阿片受体(OPRD1)内含子SNP rs2236861与非依赖性阿片类药物使用(HC与NOD)之间的关联仍然显著(比值比[OR] = 0.032;p = 0.015)。该SNP与前痛敏肽原(PNOC)SNP rs2722897表现出显著的基因 - 基因相互作用(OR = 5.24;p = 0.041)(HC与NOD)。 结论:本研究确定了几种新的以及一些先前报道的变体与海洛因依赖和非依赖性阿片类药物使用之间的关联,非依赖性阿片类药物使用者是一个重要且此前未被广泛研究的难以获取的群体。有必要进行进一步研究以证实并阐明这些变体在非法药物使用和药物成瘾易感性中的潜在作用。
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