Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder

dc.contributorHáskóli Íslandsen_US
dc.contributorUniversity of Icelanden_US
dc.contributor.authorGuðmundsson, Ólafur Ó.
dc.contributor.authorWalters, G. Bragi
dc.contributor.authorIngason, Andrés
dc.contributor.authorJohansson, Stefan
dc.contributor.authorZayats, Tetyana
dc.contributor.authorAthanasiu, Lavinia
dc.contributor.authorSonderby, Ida Elken
dc.contributor.authorGústafsson, Ómar
dc.contributor.authorNawaz, Muhammad S.
dc.contributor.authorJónsson, Guðbjörn F.
dc.contributor.authorJonsson, Lina
dc.contributor.authorKnappskog, Per-Morten
dc.contributor.authorIngvarsdóttir, Ester
dc.contributor.authorDaviðsdóttir, Katrín
dc.contributor.authorDjurovic, Srdjan
dc.contributor.authorKnudsen, Gun Peggy Strømstad
dc.contributor.authorAskeland, Ragna Bugge
dc.contributor.authorHaraldsdóttir, Gyða S.
dc.contributor.authorBaldursson, Gísli
dc.contributor.authorMagnússon, Páll
dc.contributor.authorSigurdsson, Engilbert
dc.contributor.authorGudbjartsson, Daniel
dc.contributor.authorStefansson, Hreinn
dc.contributor.authorAndreassen, Ole A.
dc.contributor.authorHaavik, Jan
dc.contributor.authorReichborn-Kjennerud, Ted
dc.contributor.authorStefansson, Kari
dc.contributor.departmentLæknadeild (HÍ)en_US
dc.contributor.departmentFaculty of Medicine (UI)en_US
dc.contributor.schoolHeilbrigðisvísindasvið (HÍ)en_US
dc.contributor.schoolSchool of Health Sciences (UI)en_US
dc.contributor.schoolSchool of Engineering and Natural Sciences (UI)en_US
dc.contributor.schoolVerkfræði- og náttúruvísindasvið (HÍ)en_US
dc.date.accessioned2020-02-12T14:21:47Z
dc.date.available2020-02-12T14:21:47Z
dc.date.issued2019-10-17
dc.descriptionPublisher's version (útgefin grein).en_US
dc.description.abstractAttention-deficit/hyperactivity disorder (ADHD) is a highly heritable common childhood-onset neurodevelopmental disorder. Some rare copy number variations (CNVs) affect multiple neurodevelopmental disorders such as intellectual disability, autism spectrum disorders (ASD), schizophrenia and ADHD. The aim of this study is to determine to what extent ADHD shares high risk CNV alleles with schizophrenia and ASD. We compiled 19 neuropsychiatric CNVs and test 14, with sufficient power, for association with ADHD in Icelandic and Norwegian samples. Eight associate with ADHD; deletions at 2p16.3 (NRXN1), 15q11.2, 15q13.3 (BP4 & BP4.5–BP5) and 22q11.21, and duplications at 1q21.1 distal, 16p11.2 proximal, 16p13.11 and 22q11.21. Six of the CNVs have not been associated with ADHD before. As a group, the 19 CNVs associate with ADHD (OR = 2.43, P = 1.6 × 10−21), even when comorbid ASD and schizophrenia are excluded from the sample. These results highlight the pleiotropic effect of the neuropsychiatric CNVs and add evidence for ADHD, ASD and schizophrenia being related neurodevelopmental disorders rather than distinct entities.en_US
dc.description.sponsorshipWe are grateful to the participants and we thank the staff at the Research Recruitment Center. We also thank the staff at deCODE genetics core facilities and all our colleagues for their important contribution to this work. We are grateful to the Benefit Society for Children with Disabilities (Styrktarfélag Lamaðra og Fatlaðra; SLF) for their participation. The research leading to these results has received support from the Innovative Medicines Initiative Joint Undertaking under grant agreements’ no. 115008 (NEWMEDS) and no. 115300 (EUAIMS), of which resources are composed of EFPIA in-kind contribution and financial contribution from the European Union’s Seventh Framework Programme (EU-FP7/2007–2013), from EU-FP7 grants no. 602450 (IMAGEMEND) and no. 502805 (Aggressotype), EU-FP7-People-2011-IAPP grant no. 286213 (PsychDPC), and The Research Council of Norway (#226971, 229129, 223273, 213694, 248778), the KG Jebsen Stiftelsen (SKGJ-MED-002 and SKGJ-MED-008), and The South-East Norway Health Authority (#2012–132).en_US
dc.description.versionPeer Revieweden_US
dc.format.extent258en_US
dc.identifier.citationGudmundsson, O.O., Walters, G.B., Ingason, A. et al. Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder. Transl Psychiatry 9, 258 (2019). https://doi.org/10.1038/s41398-019-0599-yen_US
dc.identifier.doi10.1038/s41398-019-0599-y
dc.identifier.issn2158-3188
dc.identifier.journalTranslational Psychiatryen_US
dc.identifier.urihttps://hdl.handle.net/20.500.11815/1530
dc.language.isoenen_US
dc.publisherSpringer Science and Business Media LLCen_US
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/602450en_US
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/502805is
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/286213is
dc.relation.ispartofseriesTranslational Psychiatry;9(1)
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectADHDen_US
dc.subjectComparative genomicsen_US
dc.subjectGenamengien_US
dc.subjectSamanburðarrannsókniren_US
dc.subjectErfðarannsókniren_US
dc.titleAttention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorderen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dcterms.licenseOpen Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.en_US

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