Glutamatergic and GABAergic gene sets in attention-deficit/hyperactivity disorder: association to overlapping traits in ADHD and autism
Publication year
2017Source
Translational Psychiatry, 7, (2017), article e999ISSN
Publication type
Article / Letter to editor
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Organization
Cognitive Neuroscience
PI Group MR Techniques in Brain Function
Human Genetics
Psychiatry
PI Group Memory & Emotion
Journal title
Translational Psychiatry
Volume
vol. 7
Subject
150 000 MR Techniques in Brain Function; Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience; Cognitive Neuroscience - Radboud University Medical Center; Human Genetics - Radboud University Medical Center; Psychiatry - Radboud University Medical CenterAbstract
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.
This item appears in the following Collection(s)
- Academic publications [244128]
- Donders Centre for Cognitive Neuroimaging [3984]
- Electronic publications [131089]
- Faculty of Medical Sciences [92874]
- Open Access publications [105128]
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