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

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          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.

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          Most cited references41

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          Common genetic variants on 5p14.1 associate with autism spectrum disorders.

          Autism spectrum disorders (ASDs) represent a group of childhood neurodevelopmental and neuropsychiatric disorders characterized by deficits in verbal communication, impairment of social interaction, and restricted and repetitive patterns of interests and behaviour. To identify common genetic risk factors underlying ASDs, here we present the results of genome-wide association studies on a cohort of 780 families (3,101 subjects) with affected children, and a second cohort of 1,204 affected subjects and 6,491 control subjects, all of whom were of European ancestry. Six single nucleotide polymorphisms between cadherin 10 (CDH10) and cadherin 9 (CDH9)-two genes encoding neuronal cell-adhesion molecules-revealed strong association signals, with the most significant SNP being rs4307059 (P = 3.4 x 10(-8), odds ratio = 1.19). These signals were replicated in two independent cohorts, with combined P values ranging from 7.4 x 10(-8) to 2.1 x 10(-10). Our results implicate neuronal cell-adhesion molecules in the pathogenesis of ASDs, and represent, to our knowledge, the first demonstration of genome-wide significant association of common variants with susceptibility to ASDs.
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            Neuroscience of attention-deficit/hyperactivity disorder: the search for endophenotypes.

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              Candidate gene studies of ADHD: a meta-analytic review.

              Quantitative genetic studies (i.e., twin and adoption studies) suggest that genetic influences contribute substantially to the development of attention deficit hyperactivity disorder (ADHD). Over the past 15 years, considerable efforts have been made to identify genes involved in the etiology of this disorder resulting in a large and often conflicting literature of candidate gene associations for ADHD. The first aim of the present study was to conduct a comprehensive meta-analytic review of this literature to determine which candidate genes show consistent evidence of association with childhood ADHD across studies. The second aim was to test for heterogeneity across studies in the effect sizes for each candidate gene as its presence might suggest moderating variables that could explain inconsistent results. Significant associations were identified for several candidate genes including DAT1, DRD4, DRD5, 5HTT, HTR1B, and SNAP25. Further, significant heterogeneity was observed for the associations between ADHD and DAT1, DRD4, DRD5, DBH, ADRA2A, 5HTT, TPH2, MAOA, and SNAP25, suggesting that future studies should explore potential moderators of these associations (e.g., ADHD subtype diagnoses, gender, exposure to environmental risk factors). We conclude with a discussion of these findings in relation to emerging themes relevant to future studies of the genetics of ADHD.
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                Author and article information

                Journal
                Transl Psychiatry
                Transl Psychiatry
                Translational Psychiatry
                Nature Publishing Group
                2158-3188
                January 2017
                10 January 2017
                1 January 2017
                : 7
                : 1
                : e999
                Affiliations
                [1 ]Department of Cognitive Neuroscience, Donders Institute of Brain, Cognition and Behaviour, Radboud University Medical Center , Nijmegen, The Netherlands
                [2 ]Department of Human Genetics, Radboud University Medical Center , Nijmegen, The Netherlands
                [3 ]Donders Institute for Brain, Cognition and Behaviour, Radboud University , Nijmegen, The Netherlands
                [4 ]Department of Psychiatry, Radboud University Medical Center , Nijmegen, The Netherlands
                [5 ]Karakter Child and Adolescent Psychiatry University Center , Nijmegen, The Netherlands
                Author notes
                [* ]Department of Cognitive Neuroscience, Donders Institute of Brain, Cognition and Behaviour, Radboud University Medical Center , Geert Grooteplein Noord 10 (Huispost 126), Nijmegen 6525 EZ, The Netherlands. E-mail: j.naaijen@ 123456donders.ru.nl
                [6]

                The members of the IMAGE consortium are listed above the References.

                [*]

                Stephen Faraone 1, Philip Asherson 2, Tobias Banaschewski 3, Jan Buitelaar 4, Barbara Franke 5, Richard P Ebstein 6, Michael Gill 7, Ana Miranda 8, Robert D Oades 9, Herbert Roeyers 10, Aribert Rothenberger 11, Joseph Sergeant 12, Edmund Sonuga-Barke 13, Richard Anney 14, Fernando Mulas 15 and Hans-Christoph Steinhausen 16. State University, New York 1, King's College London, Medical Research Council Social Genetic Developmental and Psychiatry Centre, Institute of Psychiatry 2, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Mannheim, Germany 3, Radboud University Medical Centre, Donders Institute for Brain, Cognition and Behavior; Karakter Child and Adolescent Psychiatry University Center, Nijmegen 4, Radboud University Medical Centre, Donders Institute for Brain, Cognition and Behaviour 5, National University of Singapore 6, Trinity College Dublin, Trinity Centre for Health Sciences and St James's Hospital, Dublin, Ireland 7, University of Valencia, Valencia, Spain 8, University of Duisburg-Essen, Clinic for Child and Adolescent Psychiatry and Psychotherapy, Essen, Germany 9, Ghent University, Ghent, Belgium 10, University of Gottingen, Gottingen, Germany 11, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands 12, University of Southampton, Developmental Brain-Behaviour Laboratory, Southampton, UK; Ghent University, Ghent, Belgium 13, Department of Psychiatry, Trinity Centre for Health Sciences, St James's Hospital, Dublin, Ireland 14, Department of Developmental and Educational Psychology, University of Valencia, Valencia, Spain 15 and University of Zurich, Zurich, Switzerland; Aalborg Psychiatric University Hospital, Aalborg, Denmark, and the University of Basel, Basel, Switzerland 16.

                Article
                tp2016273
                10.1038/tp.2016.273
                5545734
                28072412
                e3f1939c-e019-4a75-a759-bebf4b96b089
                Copyright © 2017 The Author(s)

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 01 February 2016
                : 13 November 2016
                : 27 November 2016
                Categories
                Original Article

                Clinical Psychology & Psychiatry
                Clinical Psychology & Psychiatry

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