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首页> 外文期刊>Annals of Human Genetics >Overlapping Dopaminergic Pathway Genetic Susceptibility to Heroin and Cocaine Addictions in African Americans
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Overlapping Dopaminergic Pathway Genetic Susceptibility to Heroin and Cocaine Addictions in African Americans

机译:与非洲裔美国人的海洛因和可卡因成瘾重叠的多巴胺能途径遗传易感性

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摘要

Drugs of abuse activate the mesolimbic dopaminergic pathway. Genetic variations in the dopaminergic system may contribute to drug addiction. Several processes are shared between cocaine and heroin addictions but some neurobiological mechanisms may be specific. This study examined the association of 98 single nucleotide polymorphisms in 13 dopamine-related genes with heroin addiction (OD) and/or cocaine addiction (CD) in a sample of 801 African Americans (315 subjects with OD +/- CD, 279 subjects with CD, and 207 controls). Single-marker analyses provided nominally significant evidence for associations of 24 SNPs) in DRD1, ANKK1/DRD2, DRD3, DRD5, DBH, DDC, COMT and CSNK1E. A DRD2 7-SNPs haplotype that includes SNPs rs1075650 and rs2283265, which were shown to alter D2S/D2L splicing, was indicated in both addictions. The Met allele of the functional COMT Val158Met was associated with protection from OD. None of the signals remained significant after correction for multiple testing. The study results are in accordance with the results of previous studies, including our report of association of DRD1 SNP rs5326 with OD. The findings suggest the presence of an overlap in genetic susceptibility for OD and CD, as well as shared and distinct susceptibility for OD in subjects of African and European descent.
机译:滥用药物激活培索莫氏多巴胺能途径。多巴胺能系统的遗传变异可能有助于吸毒成瘾。可卡因和海洛因成瘾之间的几种过程分享,但一些神经生物学机制可能是特异性的。该研究检测了在801名非洲裔美国人的样本中与海洛因成瘾(OD)和/或可卡因成瘾(CD)中的98个单核苷酸多态性在13种多巴胺相关基因中的关联(315个+/- CD,279名受试者CD和207个控件)。单标分析为DRD1,ANKK1 / DRD2,DRD3,DRD5,DBH,DDC,COMT和CSNK1E提供了24个SNPS关联的名义上是24个SNPS的有关证据。包括SNPS RS1075650和RS2283265的DRD2 7-SNP单倍型,其均显示为改变D2S / D2L剪接。功能性Comt Val158Met的符合等位基因与OD保护相关。在校正后,校正多次测试后,否则都没有显着。研究结果符合先前研究的结果,包括我们对DRD1 SNP RS5326与OD相关联的报告。研究结果表明,在非洲和欧洲血统受试者中,对OD和CD的遗传易感性以及对OD的共同和不同的易感性存在重叠。

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