Association Analysis of Candidate Genes for ADHD on Chromosomes 5p13, 6q12, 16p and 17p

J. Ekholm, M. N. Ogdie, J. Dang, J. McCracken, J. McGough, S. Smalley, S. Nelson
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引用次数: 1

Abstract

Attention-deficit/hyperactivity disorder (ADHD) is a common, heterogeneous psychiatric disorder of childhood displaying inattentive, hyperactive, and impulsive symptoms. Although the biological basis of ADHD remains unknown, it has been shown that genetic factors substantially contribute to the aetiology of the disorder. Our group has previously reported significant linkage to four chromosomal regions on 5p13, 6q12, 16p13 and 17p11 in genome-wide scans and subsequent fine-mapping. We selected nine positional candidate genes within the linkage intervals for study based on bio- logical plausibility. We analyzed at least 189 ADHD trios to determine if common variants in these genes have a major af- fect on ADHD risk. None yielded significant association. This does however not completely exclude these genes as poten- tial susceptibility genes for ADHD since it is plausible for common causal variants with low effect size to go undetected due to insufficient power of the study sample. We conclude that none of the tested alleles confer a major risk for develop- ing ADHD and that investigation of other genes within the linked regions is warranted.
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5p13、6q12、16p和17p染色体上ADHD候选基因的关联分析
注意缺陷/多动障碍(ADHD)是一种常见的儿童异质性精神障碍,表现为注意力不集中、多动和冲动症状。尽管ADHD的生物学基础尚不清楚,但已有研究表明,遗传因素在很大程度上影响了该疾病的病因。我们的研究小组先前在全基因组扫描和随后的精细定位中报道了与5p13、6q12、16p13和17p11上的四个染色体区域的显著联系。我们在连锁区间内选择了9个候选基因进行生物学合理性研究。我们分析了至少189个ADHD三人组,以确定这些基因的常见变异是否对ADHD风险有主要影响。没有发现显著的关联。然而,这并不能完全排除这些基因作为多动症的潜在易感基因,因为由于研究样本的不足,低效应大小的常见因果变异可能未被发现。我们的结论是,测试的等位基因中没有一个会导致ADHD的主要风险,对相关区域内的其他基因进行调查是有必要的。
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