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本文引用的文献

1
Interaction between two independent CNR1 variants increases risk for cocaine dependence in European Americans: a replication study in family-based sample and population-based sample.两个独立的CNR1变体之间的相互作用增加了欧裔美国人对可卡因依赖的风险:一项基于家系样本和人群样本的重复研究。
Neuropsychopharmacology. 2009 May;34(6):1504-13. doi: 10.1038/npp.2008.206. Epub 2008 Dec 3.
2
Evidence for association between polymorphisms in the cannabinoid receptor 1 (CNR1) gene and cannabis dependence.大麻素受体1(CNR1)基因多态性与大麻依赖之间关联的证据。
Am J Med Genet B Neuropsychiatr Genet. 2009 Jul 5;150B(5):736-40. doi: 10.1002/ajmg.b.30881.
3
PLINK: a tool set for whole-genome association and population-based linkage analyses.PLINK:一个用于全基因组关联分析和基于群体的连锁分析的工具集。
Am J Hum Genet. 2007 Sep;81(3):559-75. doi: 10.1086/519795. Epub 2007 Jul 25.
4
Role of cannabinoid type 1 receptors in locomotor activity and striatal signaling in response to psychostimulants.1型大麻素受体在对精神兴奋剂反应中的运动活性和纹状体信号传导中的作用。
J Neurosci. 2007 Jun 27;27(26):6937-47. doi: 10.1523/JNEUROSCI.3936-06.2007.
5
CNR1 variation modulates risk for drug and alcohol dependence.大麻素受体1(CNR1)基因变异调节药物和酒精依赖的风险。
Biol Psychiatry. 2007 Sep 15;62(6):616-26. doi: 10.1016/j.biopsych.2006.12.004. Epub 2007 May 23.
6
Phasic dopamine release evoked by abused substances requires cannabinoid receptor activation.滥用物质诱发的阶段性多巴胺释放需要大麻素受体激活。
J Neurosci. 2007 Jan 24;27(4):791-5. doi: 10.1523/JNEUROSCI.4152-06.2007.
7
Involvement of cannabinoid CB1 receptors in drug addiction: effects of rimonabant on behavioral responses induced by cocaine.大麻素CB1受体在药物成瘾中的作用:利莫那班对可卡因诱导的行为反应的影响。
Pharmacol Rep. 2006 Nov-Dec;58(6):806-19.
8
A tutorial on statistical methods for population association studies.群体关联研究统计方法教程。
Nat Rev Genet. 2006 Oct;7(10):781-91. doi: 10.1038/nrg1916.
9
A genomewide single-nucleotide-polymorphism panel with high ancestry information for African American admixture mapping.一个用于非裔美国人混合映射的具有高祖先信息的全基因组单核苷酸多态性面板。
Am J Hum Genet. 2006 Oct;79(4):640-9. doi: 10.1086/507954. Epub 2006 Aug 15.
10
Cannabinoid CB1 receptor antagonist AM251 inhibits cocaine-primed relapse in rats: role of glutamate in the nucleus accumbens.大麻素CB1受体拮抗剂AM251抑制大鼠可卡因诱导的复吸:伏隔核中谷氨酸的作用。
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进一步证据表明 CNR1 基因多态性与可卡因成瘾有关:在独立样本和荟萃分析中的证实。

Further evidence for association of polymorphisms in the CNR1 gene with cocaine addiction: confirmation in an independent sample and meta-analysis.

机构信息

Psychiatric Pharmacogenetics Laboratory Center for Neurobiology and Behavior Treatment Research Center Department of Psychiatry, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.

出版信息

Addict Biol. 2013 Jul;18(4):702-8. doi: 10.1111/j.1369-1600.2011.00346.x. Epub 2011 Jul 25.

DOI:10.1111/j.1369-1600.2011.00346.x
PMID:21790903
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3223560/
Abstract

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.

摘要

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。