Psychiatric disorders in children with 16p11.2 deletion and duplication.


Journal

Translational psychiatry
ISSN: 2158-3188
Titre abrégé: Transl Psychiatry
Pays: United States
ID NLM: 101562664

Informations de publication

Date de publication:
16 01 2019
Historique:
received: 16 07 2018
accepted: 13 11 2018
revised: 16 10 2018
entrez: 22 1 2019
pubmed: 22 1 2019
medline: 14 6 2019
Statut: epublish

Résumé

Deletion and duplication of 16p11.2 (BP4-BP5) have been associated with an increased risk of intellectual disability and psychiatric disorder. This is the first study to compare the frequency of a broad spectrum of psychiatric disorders in children with 16p11.2 deletion and duplication. We aimed to evaluate (1) the nature and prevalence of psychopathology associated with copy number variation (CNV) in children with 16p11.2 by comparing deletion and duplication carriers with family controls; (2) whether deletion and duplication carriers differ in frequency of psychopathology. 217 deletion carriers, 77 deletion family controls, 114 duplication carriers, and 32 duplication family controls participated in the study. Measures included standardized research diagnostic instruments. Deletion carriers had a higher frequency of any psychiatric disorder (OR = 8.9, p < 0.001), attention deficit hyperactivity disorder (ADHD) (OR = 4.0, p = 0.01), and autism spectrum disorder (ASD) (OR = 39.9, p = 0.01) than controls. Duplication carriers had a higher frequency of any psychiatric diagnosis (OR = 5.3, p = 0.01) and ADHD (OR = 7.0, p = 0.02) than controls. The prevalence of ASD in child carriers of deletions and duplications was similar (22% versus 26%). Comparison of the two CNV groups indicated a higher frequency of ADHD in children with the duplication than deletion (OR = 2.7, p = 0.04) as well as a higher frequency of overall psychiatric disorders (OR = 2.8, p = 0.02) and psychotic symptoms (OR = 4.7, p = 0.02). However, no differences between deletion and duplications carriers in the prevalence of ASD were found. Both deletion and duplication are associated with an increased risk of psychiatric disorder, supporting the importance of early recognition, diagnosis, and intervention in these groups.

Identifiants

pubmed: 30664628
doi: 10.1038/s41398-018-0339-8
pii: 10.1038/s41398-018-0339-8
pmc: PMC6341088
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

8

Subventions

Organisme : NICHD NIH HHS
ID : U54 HD083091
Pays : United States
Organisme : MRF
ID : MRF_MRF-154-0001-RG-SKUSE
Pays : United Kingdom
Organisme : Medical Research Council
ID : G0801418
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/L010305/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/L011166/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : G0800509
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/P005748/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 110222/Z/15/Z
Pays : United Kingdom
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/N022572/1
Pays : United Kingdom

Commentaires et corrections

Type : ErratumIn

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Auteurs

Maria Niarchou (M)

Division of Psychological Medicine and Clinical Neurosciences, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK. niarchoum@cardiff.ac.uk.
Institute for Molecular Bioscience, University of Queensland, Brisbane, Australia. niarchoum@cardiff.ac.uk.

Samuel J R A Chawner (SJRA)

Division of Psychological Medicine and Clinical Neurosciences, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK.

Joanne L Doherty (JL)

Division of Psychological Medicine and Clinical Neurosciences, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK.

Anne M Maillard (AM)

Centre Cantonal Autisme, Centre Hospitalier Universitaire Vaudois, University of Lausanne, Lausanne, Switzerland.

Sébastien Jacquemont (S)

Service de Génétique Médicale, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

Wendy K Chung (WK)

Departments of Pediatrics and Medicine, Columbia University, New York, NY, USA.

LeeAnne Green-Snyder (L)

Simons Foundation, New York, NY, USA.

Raphael A Bernier (RA)

Department of Psychiatry, University of Washington, Seattle, WA, USA.

Robin P Goin-Kochel (RP)

Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.

Ellen Hanson (E)

Neurodevelopmental Disorders Phenotyping Program, Divisions of Developmental Medicine and Genetics, Program in Genomics, Children's Hospital Boston, Harvard Medical School, Boston, MA, USA.
Division of Psychiatry, Children's Hospital Boston, Boston, MA, USA.

David E J Linden (DEJ)

Division of Psychological Medicine and Clinical Neurosciences, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK.

Stefanie C Linden (SC)

Division of Psychological Medicine and Clinical Neurosciences, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK.

F Lucy Raymond (FL)

Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK.

David Skuse (D)

Behavioural and Brain Sciences Unit, Institute of Child Health, University College London, London, UK.

Jeremy Hall (J)

Division of Psychological Medicine and Clinical Neurosciences, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK.
Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK.

Michael J Owen (MJ)

Division of Psychological Medicine and Clinical Neurosciences, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK.

Marianne B M van den Bree (MBMVD)

Division of Psychological Medicine and Clinical Neurosciences, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK. vandenbreemb@cardiff.ac.uk.

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