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不同证候的注意缺陷多动障碍患儿多巴胺D2受体基因携带情况检测

Determination of Dopamine D 2 Receptor Gene in Attention Deficit Hyperactivity Disorder with Different TCM Syndrome

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【作者】 李宜瑞陈晓刚李迎敏徐秋英黄福群詹淑英

【Author】 LI Yi_rui,CHEN Xiao_gang,LI Ying_min,XU Qiu_ying,HUANG Fu_qun,ZHAN Shu_ying (The First Affiliated Hospital,Guangzhou University of TCM,Guangzhou 510405,China)

【机构】 广州中医药大学第一附属医院

【摘要】 注意缺陷多动障碍(atentiondeficithypercativitydisorder,ADHD)是常见的儿童行为障碍,目前病因尚未明确。国外近年由于分子生物学方法的介入,发现多巴胺D2受体TaqIA1等位基因与本病相关。通过对广州市城镇学龄儿童多巴胺D2受体基因TaqIA多态性的检测,支持A1等位基因与本病的关系(P=0.006520);并发现该基因与中医辨证的“肾虚肝亢”证候关系更为密切(P=0.000122),而“心脾不足”证候则与正常对照组间无显著性差异(P=0.910952),因而在基因水平上为ADHD的中医辨证提供了参考思路。

【Abstract】 Attention deficit hyperactivity disorder(ADHD)is a common behavior disorder in children and its pathogenesis remains unknown.It has been reported in foreign literature that the A 1 allele of the Taq I polymorphism of the dopamine D 2 receptor gene(DRD 2)was related to ADHD.In this study,the school_age children were examined by the above technique,and the results supported the relationship between the allelic gene and ADHD(P=0.006520),especially those with the syndrome of kidney deficiency and liver hyperactivity(P=0.000122)while not related to those with the syndrome of deficiency of heart and spleen(P=0.910952).This may supply a genetic basis for the syndrome differentiation of ADHD in TCM.

【基金】 广东省中医药管理局资助
  • 【文献出处】 广州中医药大学学报 ,JOURNAL OF GUANGZHOU UNIVERSITY OF TRADITIONAL CHINESE MEDICINE , 编辑部邮箱 ,1999年01期
  • 【分类号】R277.799.4
  • 【被引频次】21
  • 【下载频次】143
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