Dept. of Child & Adolescent Mental Health, University Hospital Erlangen, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany.
kbo-Heckscher-Klinikum, München, Germany.
Sci Rep. 2017 Jun 19;7(1):3823. doi: 10.1038/s41598-017-03326-3.
In order to better understand the underpinnings of attention-deficit/hyperactivity disorder (ADHD), we targeted the relationship of attentional, cognitive control and motivational processes with DNA methylation patterns of 60 candidate genes in boys at early school age. Participants (6 to 8 years; N = 82) were selected from a German longitudinal cohort (FRANCES). ADHD-related behaviour was assessed via maternal ratings. Performance and event-related potential measures (inter alia Cue-P3 and Nogo-P3), which were recorded in a motivational go/nogo task, indicated diminished attentional orienting, reduced inhibitory response control and a larger motivational effect on performance in ADHD already at this relatively young age. Methylation patterns were analysed in buccal cell DNA with the Illumina HumanMethylation 450K array. For CpG sites at genes of the dopaminergic (COMT, ANKK1) and the neurotrophic (BDNF, NGFR) system, associations with the Nogo-P3 as well as ADHD symptom severity were found suggesting that these systems are involved in response control deficits in ADHD. Methylation effects related to both functional aspects and ADHD behaviour were also observed for DPP10 and TPH2. Epigenetic mechanisms may play a role in ADHD-associated deficits but findings need to be replicated in larger samples and are limited by the fact that only peripheral methylation could be considered.
为了更好地理解注意力缺陷多动障碍(ADHD)的基础,我们针对注意力、认知控制和动机过程与 60 个候选基因在早期学龄男孩中的 DNA 甲基化模式之间的关系进行了研究。参与者(6 至 8 岁;N=82)选自德国纵向队列(FRANCES)。通过母亲的评估来评估与 ADHD 相关的行为。在动机性 Go/Nogo 任务中记录的表现和事件相关电位测量(包括 cue-P3 和 Nogo-P3)表明,在这个相对年轻的年龄,ADHD 患者已经存在注意力定向减弱、抑制反应控制能力降低以及动机对表现的影响更大的情况。使用 Illumina HumanMethylation 450K 阵列分析了口腔细胞 DNA 中的甲基化模式。在多巴胺能(COMT、ANKK1)和神经营养(BDNF、NGFR)系统的基因中,CpG 位点与 Nogo-P3 以及 ADHD 症状严重程度相关,这表明这些系统参与了 ADHD 中的反应控制缺陷。与功能方面和 ADHD 行为相关的 DPP10 和 TPH2 也观察到了甲基化效应。表观遗传机制可能在与 ADHD 相关的缺陷中发挥作用,但这些发现需要在更大的样本中得到复制,并且受到只能考虑外周甲基化的事实的限制。