Please use this identifier to cite or link to this item: https://doi.org/10.1038/tp.2016.273
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dc.titleGlutamatergic and GABAergic gene sets in attention-deficit/hyperactivity disorder: Association to overlapping traits in ADHD and autism
dc.contributor.authorNaaijen J.
dc.contributor.authorBralten J.
dc.contributor.authorPoelmans G.
dc.contributor.authorGlennon J.C.
dc.contributor.authorFranke B.
dc.contributor.authorBuitelaar J.K.
dc.contributor.authorFaraone S.
dc.contributor.authorAsherson P.
dc.contributor.authorBanaschewski T.
dc.contributor.authorP Ebstein R.
dc.contributor.authorGill M.
dc.contributor.authorMiranda A.
dc.contributor.authorOades R.D.
dc.contributor.authorRoeyers H.
dc.contributor.authorRothenberger A.
dc.contributor.authorSergeant J.
dc.contributor.authorSonuga-Barke E.
dc.contributor.authorAnney R.
dc.contributor.authorMulas F.
dc.contributor.authorSteinhausen H.-C.
dc.contributor.authorThe Image Consortium
dc.date.accessioned2020-09-08T03:26:41Z
dc.date.available2020-09-08T03:26:41Z
dc.date.issued2017
dc.identifier.citationNaaijen J., Bralten J., Poelmans G., Glennon J.C., Franke B., Buitelaar J.K., Faraone S., Asherson P., Banaschewski T., P Ebstein R., Gill M., Miranda A., Oades R.D., Roeyers H., Rothenberger A., Sergeant J., Sonuga-Barke E., Anney R., Mulas F., Steinhausen H.-C., The Image Consortium (2017). Glutamatergic and GABAergic gene sets in attention-deficit/hyperactivity disorder: Association to overlapping traits in ADHD and autism. Translational Psychiatry 7 (1) : 273. ScholarBank@NUS Repository. https://doi.org/10.1038/tp.2016.273
dc.identifier.issn2158-3188
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/174618
dc.description.abstractAttention-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. © The Author(s) 2017.
dc.sourceUnpaywall 20200831
dc.subject4 aminobutyric acid
dc.subjectglutamic acid
dc.subjectneurotransmitter
dc.subject4 aminobutyric acid
dc.subject4 aminobutyric acid A receptor
dc.subjectAMPA receptor
dc.subjectcalcium binding protein
dc.subjectCALML5 protein, human
dc.subjectCD98 antigen
dc.subjectGABRA3 protein, human
dc.subjectGABRE protein, human
dc.subjectGABRQ protein, human
dc.subjectglutamate receptor ionotropic, AMPA 3
dc.subjectglutamic acid
dc.subjectGRIN1 protein, human
dc.subjectmetabotropic receptor
dc.subjectmetabotropic receptor 2
dc.subjectn methyl dextro aspartic acid receptor
dc.subjectnerve protein
dc.subjectNMDA receptor A1
dc.subjectSLC7A7 protein, human
dc.subjectadolescent
dc.subjectadult
dc.subjectaged
dc.subjectArticle
dc.subjectattention deficit disorder
dc.subjectautism
dc.subjectbehavior
dc.subjectchild
dc.subjectcontrolled study
dc.subjectdisease severity
dc.subjectfemale
dc.subjectGABAergic system
dc.subjectgene expression
dc.subjectgene frequency
dc.subjectgenetic association
dc.subjectgenetic risk
dc.subjectgenetic variability
dc.subjectgenotype
dc.subjectglutamatergic synapse
dc.subjecthuman
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectmulticenter study
dc.subjectneurotransmission
dc.subjectsingle nucleotide polymorphism
dc.subjectX chromosome
dc.subjectattention deficit disorder
dc.subjectautism
dc.subjectgenetics
dc.subjectmetabolism
dc.subjectpreschool child
dc.subjectpsychology
dc.subjectseverity of illness index
dc.subjectAdolescent
dc.subjectAttention Deficit Disorder with Hyperactivity
dc.subjectAutism Spectrum Disorder
dc.subjectAutistic Disorder
dc.subjectCalcium-Binding Proteins
dc.subjectChild
dc.subjectChild, Preschool
dc.subjectFemale
dc.subjectFusion Regulatory Protein 1, Light Chains
dc.subjectgamma-Aminobutyric Acid
dc.subjectGlutamic Acid
dc.subjectHumans
dc.subjectMale
dc.subjectNerve Tissue Proteins
dc.subjectReceptors, AMPA
dc.subjectReceptors, GABA-A
dc.subjectReceptors, Metabotropic Glutamate
dc.subjectReceptors, N-Methyl-D-Aspartate
dc.subjectSeverity of Illness Index
dc.typeArticle
dc.contributor.departmentPSYCHOLOGY
dc.description.doi10.1038/tp.2016.273
dc.description.sourcetitleTranslational Psychiatry
dc.description.volume7
dc.description.issue1
dc.description.page273
dc.published.statePublished
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