首页> 美国卫生研究院文献>Neuropsychiatric Disease and Treatment >A preliminary report of the dopamine receptor D4 and the dopamine transporter 1 gene polymorphism and its association with attention deficit hyperactivity disorder
【2h】

A preliminary report of the dopamine receptor D4 and the dopamine transporter 1 gene polymorphism and its association with attention deficit hyperactivity disorder

机译:多巴胺受体D4和多巴胺转运蛋白1基因多态性及其与注意缺陷多动障碍的关系的初步报道

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Attention deficit hyperactivity disorder (ADHD) is one of the most prevalent childhood-onset psychiatric syndromes affecting 5%–10% of school-age children worldwide. Distortions in the catecholaminergic system seem to be responsible for this condition. Within this system there are several candidate genes, the dopamine receptor D4 (DRD4) and the dopamine transporter 1 (DAT1), with common polymorphism which might be associated with ADHD. We performed a family based association study with 36 trios and 19 parent proband pairs. All diagnoses were confirmed by the “Hypescheme” diagnostic computer program. In this study we did not observe an association of ADHD with DRD4 and DAT1 polymorphism neither by the haplotype relative risk (HRR) method nor by the transmission disequilibrium test (TdT) method. The odds ratio for the DRD4 7-allele was 1.01 and 0.94 for both statistical tests, respectively, and the respective odds ratio for the DAT1 6-allele were 0.91 and 0.88.
机译:注意缺陷多动障碍(ADHD)是一种最普遍的儿童期精神病综合症之一,影响全世界5%至10%的学龄儿童。儿茶酚胺能系统的扭曲似乎是造成这种情况的原因。在这个系统中,有几个候选基因,多巴胺受体D4(DRD4)和多巴胺转运蛋白1(DAT1),具有可能与ADHD相关的常见多态性。我们对36个三重奏和19个父母先证者对进行了基于家庭的关联研究。所有诊断均由“ Hypescheme”诊断计算机程序确认。在这项研究中,我们既未通过单倍型相对危险度(HRR)方法也未通过透射不平衡检验(TdT)方法观察到ADHD与DRD4和DAT1多态性之间的关联。在两个统计测试中,DRD4 7等位基因的比值比分别为1.01和0.94,而DAT1 6等位基因的各自比值比为0.91和0.88。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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