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肥胖症手术相关变异与阿片类药物和可卡因成瘾人群的病例对照关联研究。

Case-control association study of WLS variants in opioid and cocaine addicted populations.

机构信息

Center for Neurobiology and Behavior, Department of Psychiatry, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA 19104, USA.

出版信息

Psychiatry Res. 2013 Jun 30;208(1):62-6. doi: 10.1016/j.psychres.2013.03.011. Epub 2013 Apr 5.

DOI:10.1016/j.psychres.2013.03.011
PMID:23566366
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3665700/
Abstract

The opioid receptor family is involved in the development and maintenance of drug addiction. The mu-opioid receptor (MOR) mediates the rewarding effects of multiple drugs, including opiates and cocaine. A number of proteins interact with MOR, potentially modulating MOR function and altering the physiological consequences of drug use. These mu-opioid receptor interacting proteins (MORIPs) are potential therapeutic targets for the treatment of addiction. The Wntless (WLS) protein was recently identified as a MORIP in a yeast two-hybrid screen. In this study, we conducted a case-control association analysis of 16 WLS genetic variants in opioid and cocaine addicted individuals of both African-American (opioid n=336, cocaine n=908) and European-American (opioid n=335, cocaine n=336) ancestry. Of the analyzed SNPs, three were nominally associated with opioid addiction and four were nominally associated with cocaine addiction. None of these associations were significant following multiple testing correction. These data suggest that the common variants of WLS analyzed in this study are not associated with opioid or cocaine addiction. However, this study does not exclude the possibilities that rare variants in WLS may affect susceptibility to drug addiction, or that common variants with small effect size may fall below the detection level of our analysis.

摘要

阿片受体家族参与了药物成瘾的发展和维持。μ-阿片受体(MOR)介导多种药物的奖赏效应,包括阿片类药物和可卡因。许多蛋白质与 MOR 相互作用,可能调节 MOR 功能并改变药物使用的生理后果。这些μ-阿片受体相互作用蛋白(MORIPs)是治疗成瘾的潜在治疗靶点。Wntless(WLS)蛋白最近在酵母双杂交筛选中被鉴定为 MORIP。在这项研究中,我们对来自非洲裔美国人(阿片类药物 n=336,可卡因 n=908)和欧洲裔美国人(阿片类药物 n=335,可卡因 n=336)的阿片类药物和可卡因成瘾个体的 16 个 WLS 遗传变异进行了病例对照关联分析。在分析的 SNP 中,有三个与阿片类药物成瘾有显著关联,四个与可卡因成瘾有显著关联。经过多次测试校正后,这些关联都没有统计学意义。这些数据表明,在这项研究中分析的 WLS 常见变体与阿片类或可卡因成瘾无关。然而,本研究不能排除 WLS 中的稀有变体可能影响药物成瘾易感性的可能性,也不能排除常见变体的效应量较小而低于我们分析的检测水平的可能性。

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本文引用的文献

1
Case-control association analysis of polymorphisms in the δ-opioid receptor, OPRD1, with cocaine and opioid addicted populations.δ-阿片受体(OPRD1)多态性与可卡因和阿片成瘾人群的病例对照关联分析。
Drug Alcohol Depend. 2013 Jan 1;127(1-3):122-8. doi: 10.1016/j.drugalcdep.2012.06.023. Epub 2012 Jul 12.
2
"Replicated" genome wide association for dependence on illegal substances: genomic regions identified by overlapping clusters of nominally positive SNPs.“依赖非法物质的复制全基因组关联研究:通过名义上阳性 SNPs 的重叠簇确定的基因组区域。”
Am J Med Genet B Neuropsychiatr Genet. 2011 Mar;156(2):125-38. doi: 10.1002/ajmg.b.31143. Epub 2010 Dec 16.
3
Ultrastructural relationship between the mu opioid receptor and its interacting protein, GPR177, in striatal neurons.纹状体神经元中μ阿片受体与其相互作用蛋白 GPR177 的超微结构关系。
Brain Res. 2010 Oct 28;1358:71-80. doi: 10.1016/j.brainres.2010.08.080. Epub 2010 Sep 21.
4
Interaction of the mu-opioid receptor with GPR177 (Wntless) inhibits Wnt secretion: potential implications for opioid dependence.μ 阿片受体与 GPR177(无尾蛋白)相互作用抑制 Wnt 分泌:对阿片类药物依赖的潜在影响。
BMC Neurosci. 2010 Mar 9;11:33. doi: 10.1186/1471-2202-11-33.
5
Reward processing by the opioid system in the brain.大脑中阿片类系统的奖赏处理
Physiol Rev. 2009 Oct;89(4):1379-412. doi: 10.1152/physrev.00005.2009.
6
Review. Genetics of addictions: strategies for addressing heterogeneity and polygenicity of substance use disorders.综述:成瘾的遗传学:应对物质使用障碍异质性和多基因性的策略
Philos Trans R Soc Lond B Biol Sci. 2008 Oct 12;363(1507):3213-22. doi: 10.1098/rstb.2008.0104.
7
Cocaine reward and hyperactivity in the rat: sites of mu opioid receptor modulation.大鼠体内可卡因奖赏与多动:μ阿片受体调节位点
Neuroscience. 2008 Jul 17;154(4):1506-16. doi: 10.1016/j.neuroscience.2008.04.063. Epub 2008 May 3.
8
Mu opioid receptor antagonists: recent developments.μ阿片受体拮抗剂:最新进展
ChemMedChem. 2007 Nov;2(11):1552-70. doi: 10.1002/cmdc.200700143.
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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。
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