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Glutamatergic and GABAergic gene sets in attention-deficit/hyperactivity disorder: association to overlapping traits in ADHD and autism
- Source :
- Translational Psychiatry, 7, Translational Psychiatry, Naaijen, J, Bralten, J, Poelmans, G, Faraone, S, Asherson, P, Banaschewski, T, Buitelaar, J, Franke, B, Ebstein, R P, Gill, M, Miranda, A, Oades, R D, Roevers, H, Rothenberger, A, Sergeant, J, Barke, E J, Anney, R, Mulas, F, Steinhausen, H C, Glennon, JC, Franke, B & Buitelaar, JK 2017, ' Glutamatergic and GABAergic gene sets in attention-deficit/hyperactivity disorder : Association to overlapping traits in ADHD and autism ', Translational psychiatry, vol. 7 . https://doi.org/10.1038/tp.2016.273
- Publication Year :
- 2017
-
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.
- Subjects :
- 0301 basic medicine
Male
Candidate gene
Adolescent
Autism Spectrum Disorder
Medizin
Glutamic Acid
Nerve Tissue Proteins
Impulsivity
Receptors, Metabotropic Glutamate
Receptors, N-Methyl-D-Aspartate
Severity of Illness Index
behavioral disciplines and activities
150 000 MR Techniques in Brain Function
03 medical and health sciences
Cellular and Molecular Neuroscience
Glutamatergic
0302 clinical medicine
mental disorders
medicine
Attention deficit hyperactivity disorder
Humans
Receptors, AMPA
Autistic Disorder
Child
Biological Psychiatry
gamma-Aminobutyric Acid
Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7]
Fusion Regulatory Protein 1, Light Chains
Calcium-Binding Proteins
Glutamate receptor
Amino Acid Transport System y+L
medicine.disease
Receptors, GABA-A
Psychiatry and Mental health
030104 developmental biology
Schizophrenia
Attention Deficit Disorder with Hyperactivity
Child, Preschool
Autism
GABAergic
Original Article
Female
medicine.symptom
Psychology
Neuroscience
030217 neurology & neurosurgery
Subjects
Details
- ISSN :
- 21583188
- Database :
- OpenAIRE
- Journal :
- Translational Psychiatry, 7, Translational Psychiatry, Naaijen, J, Bralten, J, Poelmans, G, Faraone, S, Asherson, P, Banaschewski, T, Buitelaar, J, Franke, B, Ebstein, R P, Gill, M, Miranda, A, Oades, R D, Roevers, H, Rothenberger, A, Sergeant, J, Barke, E J, Anney, R, Mulas, F, Steinhausen, H C, Glennon, JC, Franke, B & Buitelaar, JK 2017, ' Glutamatergic and GABAergic gene sets in attention-deficit/hyperactivity disorder : Association to overlapping traits in ADHD and autism ', Translational psychiatry, vol. 7 . https://doi.org/10.1038/tp.2016.273
- Accession number :
- edsair.doi.dedup.....bc5fceb0d650e8c6f99933fcbd281f9f
- Full Text :
- https://doi.org/10.1038/tp.2016.273