首页> 外文期刊>Behavioral and Brain Functions >Dopamine-beta hydroxylase polymorphism and cocaine addiction
【24h】

Dopamine-beta hydroxylase polymorphism and cocaine addiction

机译:多巴胺-β羟化酶多态性与可卡因成瘾

获取原文
           

摘要

Cocaine addiction involves a number of medical, psychological and social problems. Understanding the genetic aetiology of this disorder will be essential for design of effective treatments. Dopamine-beta hydroxylase (DbH) catalyzes the conversion of dopamine to norepinephrine and could, therefore, have an influence on both cocaine action and the basal sensitivity of neurotransmitter systems to cocaine. Recently, the -1021C>T polymorphism have been found to strongly correlated with individual variation in plasma DbH activity. To test the influence of this polymorphism on the susceptibility of cocaine addiction, we decided to genotype it in a sample of 689 cocaine addicts and 832 healthy individuals. Genotypic and allelic analyses did not show any evidence of association with cocaine addiction, even after correcting for the effect of population stratification and other possible confounders. Our results do not support a major role of the -1021C>T polymorphism or the gene itself in the development of cocaine addiction but further examination of other variants within this gene will be necessary to completely rule out an effect.
机译:可卡因成瘾涉及许多医学,心理和社会问题。了解这种疾病的遗传病因对设计有效的治疗方法至关重要。多巴胺-β羟化酶(DbH)催化多巴胺向去甲肾上腺素的转化,因此可能对可卡因的作用和神经递质系统对可卡因的基础敏感性都有影响。最近,已发现-1021C> T多态性与血浆DbH活性的个体变化密切相关。为了测试这种多态性对可卡因成瘾敏感性的影响,我们决定对689名可卡因成瘾者和832个健康个体的样本进行基因分型。基因型和等位基因分析没有显示出与可卡因成瘾有关的任何证据,即使在校正了人口分层和其他可能的混杂因素的影响之后。我们的结果不支持-1021C> T多态性或该基因本身在可卡因成瘾发展中的主要作用,但必须进一步检查该基因内的其他变异体才能完全排除这种作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号