Psychiatric Pharmacogenetics Laboratory Center for Neurobiology and Behavior Treatment Research Center Department of Psychiatry, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
Addict Biol. 2013 Jul;18(4):702-8. doi: 10.1111/j.1369-1600.2011.00346.x. Epub 2011 Jul 25.
Genetic research on cocaine dependence (CD) may help clarify our understanding of the disorder as well as provide insights for effective treatment. As endocannabinoid signaling and dopamine neurotransmission have been shown to be involved in drug reward, genes related to these systems are plausible candidates for susceptibility to CD. The cannabinoid receptor 1 protein regulates both the endocannabinoid and dopaminergic neurobiological systems, and polymorphisms in the cannabinoid receptor gene, CNR1, have been associated previously with substance dependence. In this study, we attempt to replicate findings associating CNR1 with CD in African Americans. Cocaine-addicted individuals (n=860) and unaffected controls (n=334) of African descent were genotyped for two single nucleotide polymorphisms (SNPs) in CNR1 (rs6454674, rs806368). We observed a significant difference in genotype frequencies between cases and controls for both SNPs (P≤0.042). A meta-analysis was also performed combining our data with that of Zuo et al. who also studied these polymorphisms in African American cocaine addicts (total n=1253 cases versus 543 controls). When our data were combined, rs6454674 increased in significance to P=0.027; however, rs806368 was no longer significant. This study confirms the association between rs6454674 and CD. However, because there is considerable co-morbidity of CD with other drugs of abuse, additional studies are necessary to determine whether polymorphisms in CNR1 induce a general susceptibility to substance dependence or are specific to cocaine addiction. Furthermore, as this population consists of American individuals of African descent, the possibility of population stratification should not be excluded.
可卡因依赖(CD)的遗传研究可能有助于阐明我们对该疾病的理解,并为有效治疗提供思路。内源性大麻素信号和多巴胺神经递质已被证明参与了药物奖赏,因此与这些系统相关的基因可能是易患 CD 的合理候选者。大麻素受体 1 蛋白调节内源性大麻素和多巴胺能神经生物学系统,大麻素受体基因 CNR1 的多态性先前与物质依赖有关。在这项研究中,我们试图复制 CNR1 与非洲裔美国人 CD 相关的发现。对具有可卡因依赖的个体(n=860)和未受影响的对照组(n=334)进行了 CNR1 中两个单核苷酸多态性(SNPs)的基因分型:rs6454674 和 rs806368。我们观察到两个 SNP 的病例和对照组之间的基因型频率存在显著差异(P≤0.042)。还对我们的数据与 Zuo 等人的数据进行了荟萃分析,他们也研究了这两个 SNP 在非洲裔美国可卡因成瘾者中的作用(总病例数为 1253 例,对照组为 543 例)。当我们的数据合并后,rs6454674 的显著性增加到 P=0.027;然而,rs806368 不再显著。这项研究证实了 rs6454674 与 CD 之间的关联。然而,由于 CD 与其他滥用药物的共病率相当高,因此需要进行更多的研究来确定 CNR1 中的多态性是否会导致对物质依赖的普遍易感性,还是仅对可卡因成瘾具有特异性。此外,由于该人群由具有非洲血统的美国个体组成,因此不应排除群体分层的可能性。