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以定量性状衡量的注意力不集中和多动-冲动的全基因组关联研究。

Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.

作者信息

Ebejer Jane L, Duffy David L, van der Werf Julius, Wright Margaret J, Montgomery Grant, Gillespie Nathan A, Hickie Ian B, Martin Nicholas G, Medland Sarah E

机构信息

School of Environmental and Rural Sciences, University of New England, Armidale, New South Wales, Australia.

出版信息

Twin Res Hum Genet. 2013 Apr;16(2):560-74. doi: 10.1017/thg.2013.12.

Abstract

Genome-wide association studies (GWAS) of attention-deficit/hyperactivity disorder (ADHD) offer the benefit of a hypothesis-free approach to measuring the quantitative effect of genetic variants on affection status. Generally the findings of GWAS relying on ADHD status have been non-significant, but the one study using quantitative measures of symptoms found SLC9A9 and SLC6A1 were associated with inattention and hyperactivity-impulsivity. Accordingly, we performed a GWAS using quantitative measures of each ADHD subtype measured with the Strengths and Weaknesses of ADHD and Normal Behaviour (SWAN) scale in two community-based samples. This scale captures the full range of attention and kinetic behavior; from high levels of attention and appropriate activity to the inattention and hyperactivity-impulsivity associated with ADHD within two community-based samples. Our discovery sample comprised 1,851 participants (mean age = 22.8 years [4.8]; 50.6% female), while our replication sample comprised 155 participants (mean age = 26.3 years [3.1]; 68.4% females). Age, sex, age × sex, and age2 were included as covariates and the results from each sample were combined using meta-analysis, then analyzed with a gene-based test to estimate the combined effect of markers within genes. We compare our results with markers that have previously been found to have a strong association with ADHD symptoms. Neither the GWAS nor subsequent meta-analyses yielded genome-wide significant results; the strongest effect was observed at rs2110267 (4.62 × 10-7) for symptoms of hyperactivity-impulsivity. The strongest effect in the gene-based test was for GPR139 on symptoms of inattention (6.40 × 10-5). Replication of this study with larger samples will add to our understanding of the genetic etiology of ADHD.

摘要

注意力缺陷多动障碍(ADHD)的全基因组关联研究(GWAS)提供了一种无假设方法的优势,用于测量基因变异对患病状态的定量影响。一般来说,依赖ADHD状态的GWAS研究结果并不显著,但一项使用症状定量测量的研究发现,SLC9A9和SLC6A1与注意力不集中和多动冲动有关。因此,我们在两个基于社区的样本中,使用ADHD及正常行为的优势与劣势(SWAN)量表对每种ADHD亚型进行定量测量,开展了一项GWAS。该量表涵盖了注意力和运动行为的全范围;从高度注意力和适当活动到两个基于社区的样本中与ADHD相关的注意力不集中和多动冲动。我们的发现样本包括1851名参与者(平均年龄 = 22.8岁[4.8];50.6%为女性),而我们的复制样本包括155名参与者(平均年龄 = 26.3岁[3.1];68.4%为女性)。将年龄、性别、年龄×性别和年龄²作为协变量,并使用荟萃分析合并每个样本的结果,然后通过基于基因的测试进行分析,以估计基因内标记的综合效应。我们将我们的结果与先前发现与ADHD症状有强关联的标记进行比较。GWAS及后续的荟萃分析均未产生全基因组显著结果;在rs2110267处观察到多动冲动症状的最强效应(4.62×10⁻⁷)。基于基因的测试中,对注意力不集中症状影响最强的是GPR139(6.40×10⁻⁵)。用更大样本对本研究进行复制,将增进我们对ADHD遗传病因的理解。

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