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注意力缺陷多动障碍中的谷氨酸能和γ-氨基丁酸能基因集:与多动症和自闭症重叠特征的关联

Glutamatergic and GABAergic gene sets in attention-deficit/hyperactivity disorder: association to overlapping traits in ADHD and autism.

作者信息

Naaijen J, Bralten J, Poelmans G, Glennon J C, Franke B, Buitelaar J K

机构信息

Department of Cognitive Neuroscience, Donders Institute of Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.

Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.

出版信息

Transl Psychiatry. 2017 Jan 10;7(1):e999. doi: 10.1038/tp.2016.273.

DOI:10.1038/tp.2016.273
PMID:28072412
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5545734/
Abstract

Attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorders (ASD) often co-occur. Both are highly heritable; however, it has been difficult to discover genetic risk variants. Glutamate and GABA are main excitatory and inhibitory neurotransmitters in the brain; their balance is essential for proper brain development and functioning. In this study we investigated the role of glutamate and GABA genetics in ADHD severity, autism symptom severity and inhibitory performance, based on gene set analysis, an approach to investigate multiple genetic variants simultaneously. Common variants within glutamatergic and GABAergic genes were investigated using the MAGMA software in an ADHD case-only sample (n=931), in which we assessed ASD symptoms and response inhibition on a Stop task. Gene set analysis for ADHD symptom severity, divided into inattention and hyperactivity/impulsivity symptoms, autism symptom severity and inhibition were performed using principal component regression analyses. Subsequently, gene-wide association analyses were performed. The glutamate gene set showed an association with severity of hyperactivity/impulsivity (P=0.009), which was robust to correcting for genome-wide association levels. The GABA gene set showed nominally significant association with inhibition (P=0.04), but this did not survive correction for multiple comparisons. None of single gene or single variant associations was significant on their own. By analyzing multiple genetic variants within candidate gene sets together, we were able to find genetic associations supporting the involvement of excitatory and inhibitory neurotransmitter systems in ADHD and ASD symptom severity in ADHD.

摘要

注意缺陷多动障碍(ADHD)和自闭症谱系障碍(ASD)常常同时出现。二者都具有高度遗传性;然而,发现遗传风险变异一直很困难。谷氨酸和γ-氨基丁酸(GABA)是大脑中主要的兴奋性和抑制性神经递质;它们的平衡对于大脑的正常发育和功能至关重要。在本研究中,我们基于基因集分析(一种同时研究多个遗传变异的方法),调查了谷氨酸和GABA遗传学在ADHD严重程度、自闭症症状严重程度及抑制功能方面的作用。我们使用MAGMA软件在一个仅包含ADHD病例的样本(n = 931)中研究了谷氨酸能和GABA能基因中的常见变异,在该样本中我们评估了自闭症症状以及停止任务中的反应抑制情况。使用主成分回归分析对ADHD症状严重程度(分为注意力不集中和多动/冲动症状)、自闭症症状严重程度及抑制功能进行了基因集分析。随后,进行了全基因关联分析。谷氨酸基因集显示与多动/冲动严重程度相关(P = 0.009),在对全基因组关联水平进行校正后该结果依然稳健。GABA基因集显示与抑制功能有名义上的显著关联(P = 0.04),但在多重比较校正后该结果不再显著。单个基因或单个变异的关联本身均无显著意义。通过一起分析候选基因集中的多个遗传变异,我们能够找到遗传关联,支持兴奋性和抑制性神经递质系统参与ADHD严重程度以及ADHD中的ASD症状严重程度。