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Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants

OBJECTIVE: Attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) often co-occur and share genetic risks. The aim of this analysis was to determine more broadly whether ADHD and ASD share biological underpinnings. METHOD: We compared copy number variant (CNV) data from 72...

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Autores principales: Martin, Joanna, Cooper, Miriam, Hamshere, Marian L., Pocklington, Andrew, Scherer, Stephen W., Kent, Lindsey, Gill, Michael, Owen, Michael J., Williams, Nigel, O'Donovan, Michael C., Thapar, Anita, Holmans, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4074351/
https://www.ncbi.nlm.nih.gov/pubmed/24954825
http://dx.doi.org/10.1016/j.jaac.2014.03.004
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author Martin, Joanna
Cooper, Miriam
Hamshere, Marian L.
Pocklington, Andrew
Scherer, Stephen W.
Kent, Lindsey
Gill, Michael
Owen, Michael J.
Williams, Nigel
O'Donovan, Michael C.
Thapar, Anita
Holmans, Peter
author_facet Martin, Joanna
Cooper, Miriam
Hamshere, Marian L.
Pocklington, Andrew
Scherer, Stephen W.
Kent, Lindsey
Gill, Michael
Owen, Michael J.
Williams, Nigel
O'Donovan, Michael C.
Thapar, Anita
Holmans, Peter
author_sort Martin, Joanna
collection PubMed
description OBJECTIVE: Attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) often co-occur and share genetic risks. The aim of this analysis was to determine more broadly whether ADHD and ASD share biological underpinnings. METHOD: We compared copy number variant (CNV) data from 727 children with ADHD and 5,081 population controls to data from 996 individuals with ASD and an independent set of 1,287 controls. Using pathway analyses, we investigated whether CNVs observed in individuals with ADHD have an impact on genes in the same biological pathways as on those observed in individuals with ASD. RESULTS: The results suggest that the biological pathways affected by CNVs in ADHD overlap with those affected by CNVs in ASD more than would be expected by chance. Moreover, this was true even when specific CNV regions common to both disorders were excluded from the analysis. After correction for multiple testing, genes involved in 3 biological processes (nicotinic acetylcholine receptor signalling pathway, cell division, and response to drug) showed significant enrichment for case CNV hits in the combined ADHD and ASD sample. CONCLUSION: The results of this study indicate the presence of significant overlap of shared biological processes disrupted by large rare CNVs in children with these 2 neurodevelopmental conditions.
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spelling pubmed-40743512014-07-07 Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants Martin, Joanna Cooper, Miriam Hamshere, Marian L. Pocklington, Andrew Scherer, Stephen W. Kent, Lindsey Gill, Michael Owen, Michael J. Williams, Nigel O'Donovan, Michael C. Thapar, Anita Holmans, Peter J Am Acad Child Adolesc Psychiatry New Research OBJECTIVE: Attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) often co-occur and share genetic risks. The aim of this analysis was to determine more broadly whether ADHD and ASD share biological underpinnings. METHOD: We compared copy number variant (CNV) data from 727 children with ADHD and 5,081 population controls to data from 996 individuals with ASD and an independent set of 1,287 controls. Using pathway analyses, we investigated whether CNVs observed in individuals with ADHD have an impact on genes in the same biological pathways as on those observed in individuals with ASD. RESULTS: The results suggest that the biological pathways affected by CNVs in ADHD overlap with those affected by CNVs in ASD more than would be expected by chance. Moreover, this was true even when specific CNV regions common to both disorders were excluded from the analysis. After correction for multiple testing, genes involved in 3 biological processes (nicotinic acetylcholine receptor signalling pathway, cell division, and response to drug) showed significant enrichment for case CNV hits in the combined ADHD and ASD sample. CONCLUSION: The results of this study indicate the presence of significant overlap of shared biological processes disrupted by large rare CNVs in children with these 2 neurodevelopmental conditions. Elsevier 2014-07 /pmc/articles/PMC4074351/ /pubmed/24954825 http://dx.doi.org/10.1016/j.jaac.2014.03.004 Text en © 2014 American Academy of Child and Adolescent Psychiatry. Published by Elsevier Inc. All rights reserved. https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/) .
spellingShingle New Research
Martin, Joanna
Cooper, Miriam
Hamshere, Marian L.
Pocklington, Andrew
Scherer, Stephen W.
Kent, Lindsey
Gill, Michael
Owen, Michael J.
Williams, Nigel
O'Donovan, Michael C.
Thapar, Anita
Holmans, Peter
Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants
title Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants
title_full Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants
title_fullStr Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants
title_full_unstemmed Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants
title_short Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants
title_sort biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4074351/
https://www.ncbi.nlm.nih.gov/pubmed/24954825
http://dx.doi.org/10.1016/j.jaac.2014.03.004
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