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多巴胺D4受体基因多态性与注意力缺陷多动障碍有关。

Dopamine D4 receptor gene polymorphism is associated with attention deficit hyperactivity disorder.

作者信息

LaHoste G J, Swanson J M, Wigal S B, Glabe C, Wigal T, King N, Kennedy J L

机构信息

Department of Physical Medicine and Rehabilitation, University of California, Irvine 92717-4550, USA.

出版信息

Mol Psychiatry. 1996 May;1(2):121-4.

PMID:9118321
Abstract

Dopamine is believed to play a major role in the manifestation of attention deficit hyperactivity disorder (ADHD), which affects 3-6% of school-age children and shows evidence of familiarity. The dopamine D4 receptor, which is preferentially distributed in cortical and limbic regions of the brain, is currently of major interest because of the high degree of functionally relevant variability in its gene (DRD4), and the association of this gene with Novelty Seeking behavior. We examined the variability in the length of a region of DRD4 that contains a 48-bp repeat sequence in children with ADHD and controls matched for ethnicity. ADHD children differed from controls in that the 7-fold repeat form of DRD4 occurred significantly more frequently than in the control sample. This form of the receptor has previously been shown to mediate a blunted intracellular response to dopamine. Although ADHD is likely to be multifactorial in its etiology and its heritability is likely to be polygenetic, the present findings suggest that polymorphic variation in the gene encoding the D4 dopamine receptor may be a contributing factor in the expression of symptoms associated with ADHD.

摘要

多巴胺被认为在注意力缺陷多动障碍(ADHD)的表现中起主要作用,ADHD影响3%至6%的学龄儿童,并有家族遗传迹象。多巴胺D4受体优先分布于大脑皮质和边缘区域,由于其基因(DRD4)在功能上具有高度相关的变异性,且该基因与寻求新奇行为有关联,目前备受关注。我们检测了患有ADHD的儿童以及种族匹配的对照组中,DRD4基因一个包含48个碱基对重复序列区域的长度变异性。ADHD儿童与对照组的不同之处在于,DRD4的7倍重复形式出现的频率显著高于对照组样本。此前已表明,这种形式的受体介导对多巴胺的细胞内反应减弱。尽管ADHD的病因可能是多因素的,其遗传性可能是多基因的,但目前的研究结果表明,编码D4多巴胺受体的基因多态性变异可能是ADHD相关症状表达的一个促成因素。

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