首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Association analysis between polymorphisms in the conserved dopamine neurotrophic factor (CDNF) gene and cocaine dependence.
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Association analysis between polymorphisms in the conserved dopamine neurotrophic factor (CDNF) gene and cocaine dependence.

机译:保守的多巴胺神经营养因子(CDNF)基因多态性与可卡因依赖性之间的关联分析。

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Cocaine-induced neuroplasticity changes in the mesocorticolimbic dopamine systems are thought to be involved in the pathophysiology of cocaine dependence. Since neurotrophic factors have been observed to prevent/reverse and mimic cocaine-induced neurobiological changes in the brain, related genes are plausible candidates for susceptibility to cocaine dependence. The novel conserved dopamine neurotrophic factor protein (CDNF) promotes the survival, growth, and function of dopamine-specific neurons and is expressed in brain regions that undergo cocaine-induced neuroplasticity. In this study, we hypothesize that polymorphisms in the CDNF gene (CDNF/ARMETL1) contribute to increased risk for cocaine dependence. Cocaine dependent individuals (n=351) and unaffected controls (n=257) of African descent were genotyped for four single nucleotide polymorphisms (SNPs) in the CDNF gene (rs11259365, rs7094179, rs7900873, rs2278871). We observed no significant differences in allele, genotype, or haplotype frequencies between cases and controls for any of the tested SNPs. Our study suggests that there is no association between variants in the CDNF gene and cocaine dependence. However, additional studies using larger sample sizes, comprehensive SNP coverage, and clinically homogenous populations are necessary before confidently excluding CDNF as a significant genetic risk factor for cocaine dependence.
机译:可卡因引起的中皮层皮质多巴胺系统神经可塑性的变化被认为与可卡因依赖有关。由于已经观察到神经营养因子可以预防/逆转和模仿可卡因诱导的大脑神经生物学变化,因此相关基因是可卡因依赖敏感性的合理候选者。新型保守的多巴胺神经营养因子蛋白(CDNF)促进多巴胺特异性神经元的存活,生长和功能,并在经历可卡因诱导的神经可塑性的大脑区域表达。在这项研究中,我们假设CDNF基因(CDNF / ARMETL1)的多态性有助于增加可卡因依赖的风险。对可卡因依赖的个体(n = 351)和未受影响的非洲人后裔对照(n = 257)进行了基因分型,分析了CDNF基因中的四个单核苷酸多态性(SNP)(rs11259365,rs7094179,rs7900873,rs2278871)。我们没有观察到病例和对照之间的等位基因,基因型或单倍型频率存在任何显着差异。我们的研究表明,CDNF基因的变异与可卡因依赖性之间没有关联。但是,在确信将CDNF排除为可卡因依赖的重要遗传危险因素之前,需要进行更多的研究,使用较大的样本量,全面的SNP覆盖范围以及临床上均一的种群。

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