Martin Joanna, Cooper Miriam, Hamshere Marian L, Pocklington Andrew, Scherer Stephen W, Kent Lindsey, Gill Michael, Owen Michael J, Williams Nigel, O'Donovan Michael C, Thapar Anita, Holmans Peter
MRC Centre for Neuropsychiatric Genetics and Genomics, Institute of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, UK.
MRC Centre for Neuropsychiatric Genetics and Genomics, Institute of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, UK.
J Am Acad Child Adolesc Psychiatry. 2014 Jul;53(7):761-70.e26. doi: 10.1016/j.jaac.2014.03.004. Epub 2014 Apr 21.
Attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) often co-occur and share genetic risks. The aim of this analysis was to determine more broadly whether ADHD and ASD share biological underpinnings.
We compared copy number variant (CNV) data from 727 children with ADHD and 5,081 population controls to data from 996 individuals with ASD and an independent set of 1,287 controls. Using pathway analyses, we investigated whether CNVs observed in individuals with ADHD have an impact on genes in the same biological pathways as on those observed in individuals with ASD.
The results suggest that the biological pathways affected by CNVs in ADHD overlap with those affected by CNVs in ASD more than would be expected by chance. Moreover, this was true even when specific CNV regions common to both disorders were excluded from the analysis. After correction for multiple testing, genes involved in 3 biological processes (nicotinic acetylcholine receptor signalling pathway, cell division, and response to drug) showed significant enrichment for case CNV hits in the combined ADHD and ASD sample.
The results of this study indicate the presence of significant overlap of shared biological processes disrupted by large rare CNVs in children with these 2 neurodevelopmental conditions.
注意力缺陷多动障碍(ADHD)和自闭症谱系障碍(ASD)常同时出现且存在共同的遗传风险。本分析的目的是更广泛地确定ADHD和ASD是否具有共同的生物学基础。
我们将727名ADHD儿童和5081名群体对照的拷贝数变异(CNV)数据与996名ASD个体及另一组独立的1287名对照的数据进行比较。通过通路分析,我们研究了在ADHD个体中观察到的CNV是否对与ASD个体中观察到的相同生物学通路中的基因产生影响。
结果表明,ADHD中受CNV影响的生物学通路与ASD中受CNV影响的生物学通路的重叠程度高于偶然预期。此外,即使在分析中排除了两种疾病共有的特定CNV区域,情况依然如此。在进行多重检验校正后,参与3种生物学过程(烟碱型乙酰胆碱受体信号通路、细胞分裂和药物反应)的基因在合并的ADHD和ASD样本中显示出病例CNV命中的显著富集。
本研究结果表明,在这两种神经发育疾病的儿童中,由大型罕见CNV破坏的共享生物学过程存在显著重叠。