Quist J F, Barr C L, Schachar R, Roberts W, Malone M, Tannock R, Basile V S, Beitchman J, Kennedy J L
Neurogentics Section, Centre for Addiction and Mental Health, Clarke Division, and Department of Psychiatry, University of Toronto, Canada.
Mol Psychiatry. 2003 Jan;8(1):98-102. doi: 10.1038/sj.mp.4001244.
Recent research has suggested that serotonin, in addition to dopamine, may be involved in the development of attention deficit hyperactivity disorder (ADHD). Serotonin regulates dopaminergic neurotransmission in some areas of the brain via several 5-HT receptors including 5-HT1B. Animal studies have suggested the involvement of the 5-HT1B receptors in locomotor behaviour. For these reasons, we hypothesized that the 5-HT1B receptor gene may be a good candidate for genetic studies of ADHD. We tested for linkage disequilibrium between the 5-HT1B G861C polymorphism and ADHD in 115 families using the transmission disequilibrium test (TDT). We found evidence for a trend towards excess transmission of the 861G allele (chi(2) = 2.91, P = 0.09) that when further analysed for parental allele transmissions exhibited significantly greater paternal transmission of the G allele (chi(2) = 4.80, P = 0.03) to the affected child. Although preliminary, results from this study provide additional evidence that serotonin genes may be important risk factors for the development of ADHD.
最近的研究表明,除多巴胺外,血清素可能也与注意力缺陷多动障碍(ADHD)的发病有关。血清素通过包括5-HT1B在内的几种5-羟色胺受体,调节大脑某些区域的多巴胺能神经传递。动物研究表明5-HT1B受体与运动行为有关。基于这些原因,我们推测5-HT1B受体基因可能是ADHD基因研究的一个良好候选对象。我们使用传递不平衡检验(TDT),对115个家庭中5-HT1B G861C多态性与ADHD之间的连锁不平衡进行了检测。我们发现有证据表明861G等位基因存在过度传递的趋势(卡方=2.91,P=0.09);进一步分析亲代等位基因传递情况时发现,G等位基因从父亲向患病子女的传递显著更多(卡方=4.80,P=0.03)。尽管本研究结果尚属初步,但为血清素基因可能是ADHD发病的重要风险因素提供了更多证据。