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与持续性 ADHD 相关的 DNA 甲基化表明 TARBP1 是一个新的候选基因。

DNA methylation associated with persistent ADHD suggests TARBP1 as novel candidate.

机构信息

Department of Molecular Genetics, Institute of Cell Biology (Cancer Research), University of Duisburg-Essen, Essen, Germany; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.

Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.

出版信息

Neuropharmacology. 2021 Feb 15;184:108370. doi: 10.1016/j.neuropharm.2020.108370. Epub 2020 Oct 31.

Abstract

Attention-deficit/hyperactivity disorder (ADHD) is a neurodevelopmental disorder characterized by age-inappropriate symptoms of inattention and/or hyperactivity and impulsivity. ADHD is highly prevalent in childhood and often persists into adulthood. Both genetic variants and environmental factors play a role in the onset and persistence of ADHD, and epigenetic changes, such as DNA methylation are considered as a link for their interplay. To investigate this, we studied DNA methylation in 37 candidate genes by performing targeted bisulfite sequencing of DNA isolated from whole blood of N = 88 individuals diagnosed with adult ADHD and N = 91 unaffected individuals (mean age 34.2 years). Differentially methylated sites were assessed by generalized linear models testing ADHD status and ADHD symptoms, accounting for a methylation-based smoking score, age, sex, and blood cell count. DNA methylation of single sites within DRD4 and KLDR1 was associated with adult ADHD status, and multiple DNA methylation sites within TARBP1 were associated with ADHD symptoms in adulthood and childhood. Awaiting replication, findings of this pilot study point to TARBP1 as a new candidate gene for ADHD symptoms. Our work also stresses the need for research to further examine the effects of environmental factors, such as nicotine exposure, on epigenetic modifications associated with psychiatric traits.

摘要

注意缺陷多动障碍(ADHD)是一种神经发育障碍,其特征是注意力不集中和/或多动和冲动的年龄不适当症状。ADHD 在儿童中非常普遍,并且经常持续到成年。遗传变异和环境因素都在 ADHD 的发病和持续中起作用,表观遗传变化,如 DNA 甲基化,被认为是它们相互作用的联系。为了研究这一点,我们通过对来自 88 名被诊断为成人 ADHD 的个体和 91 名未受影响的个体(平均年龄 34.2 岁)的全血中分离的 DNA 进行靶向亚硫酸氢盐测序,研究了 37 个候选基因的 DNA 甲基化。通过广义线性模型测试 ADHD 状态和 ADHD 症状评估差异甲基化位点,考虑基于甲基化的吸烟评分、年龄、性别和血细胞计数。DRD4 和 KLDR1 内的单个位点的 DNA 甲基化与成人 ADHD 状态相关,而 TARBP1 内的多个 DNA 甲基化位点与成年和儿童时期的 ADHD 症状相关。在等待复制的情况下,这项初步研究的结果表明 TARBP1 是 ADHD 症状的一个新候选基因。我们的工作还强调需要进一步研究环境因素(如尼古丁暴露)对与精神特征相关的表观遗传修饰的影响。

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