Association of the steroid sulfatase (STS) gene with attention deficit hyperactivity disorder.

K J Brookes, Z Hawi, A Kirley, E Barry, M Gill, L Kent
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引用次数: 63

Abstract

Attention deficit hyperactivity disorder (ADHD) is the most common behavioral disorder affecting children worldwide. The male bias in the prevalence of the disorder, suggests that some susceptibility genes may lie on the X chromosome. In this study we present evidence for a role of the X-linked steroid sulfatase (STS) gene and neurosteroids in the development of ADHD. Previously it has been observed that probands with ADHD have lower serum concentrations of the neurosteroids DHEA, which is synthesized from DHEA-S by STS. In further support, boys that suffer from XLI, a skin disorder caused by the deletion of the STS gene, have higher rates of ADHD, in particular the inattentive subtype. In a moderately sized sample of ADHD families (N = 384), we genotyped seven single nucleotide polymorphisms, tagging the entire gene. TDT analysis of the data yielded two polymorphisms that were significantly associated with ADHD (rs2770112-Transmitted: 71 Not Transmitted; 48; rs12861247-Transmitted: 43 Not Transmitted: 21), located towards the 5' end of the gene (P < 0.05). We conclude that the STS gene may play a role in susceptibility for ADHD, and that the neurosteroids pathways should be investigated further to access their potential contribution in susceptibility to the disorder.

类固醇硫酸酯酶(STS)基因与注意缺陷多动障碍的关系。
注意缺陷多动障碍(ADHD)是影响全世界儿童的最常见的行为障碍。男性对这种疾病的偏爱表明,某些易感基因可能位于X染色体上。在这项研究中,我们提出了x连锁类固醇硫酸酯酶(STS)基因和神经类固醇在ADHD发展中的作用的证据。先前已经观察到ADHD先显子的血清中神经类固醇脱氢表雄酮(DHEA)浓度较低,脱氢表雄酮是通过STS从脱氢表雄酮s合成的。进一步的证据表明,患有XLI(一种由STS基因缺失引起的皮肤疾病)的男孩患多动症的几率更高,尤其是注意力不集中亚型。在中等大小的ADHD家族样本中(N = 384),我们对7个单核苷酸多态性进行了基因分型,标记了整个基因。数据的TDT分析产生了两个与ADHD显著相关的多态性(rs2770112-遗传:71 -未遗传;48;rs12861247-已传:43未传:21),位于基因5'端(P < 0.05)。我们的结论是,STS基因可能在ADHD易感性中起作用,神经类固醇通路应进一步研究,以获得其对ADHD易感性的潜在贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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