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Psychiatric disorders in children with 16p11.2 deletion and duplication
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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341088/ https://www.ncbi.nlm.nih.gov/pubmed/30664628 http://dx.doi.org/10.1038/s41398-018-0339-8 |
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author | Niarchou, Maria Chawner, Samuel J. R. A. Doherty, Joanne L. Maillard, Anne M. Jacquemont, Sébastien Chung, Wendy K. Green-Snyder, LeeAnne Bernier, Raphael A. Goin-Kochel, Robin P. Hanson, Ellen Linden, David E. J. Linden, Stefanie C. Raymond, F. Lucy Skuse, David Hall, Jeremy Owen, Michael J. Bree, Marianne B. M. van den |
author_facet | Niarchou, Maria Chawner, Samuel J. R. A. Doherty, Joanne L. Maillard, Anne M. Jacquemont, Sébastien Chung, Wendy K. Green-Snyder, LeeAnne Bernier, Raphael A. Goin-Kochel, Robin P. Hanson, Ellen Linden, David E. J. Linden, Stefanie C. Raymond, F. Lucy Skuse, David Hall, Jeremy Owen, Michael J. Bree, Marianne B. M. van den |
author_sort | Niarchou, Maria |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6341088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63410882019-01-23 Psychiatric disorders in children with 16p11.2 deletion and duplication Niarchou, Maria Chawner, Samuel J. R. A. Doherty, Joanne L. Maillard, Anne M. Jacquemont, Sébastien Chung, Wendy K. Green-Snyder, LeeAnne Bernier, Raphael A. Goin-Kochel, Robin P. Hanson, Ellen Linden, David E. J. Linden, Stefanie C. Raymond, F. Lucy Skuse, David Hall, Jeremy Owen, Michael J. Bree, Marianne B. M. van den Transl Psychiatry Article 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. Nature Publishing Group UK 2019-01-16 /pmc/articles/PMC6341088/ /pubmed/30664628 http://dx.doi.org/10.1038/s41398-018-0339-8 Text en © The Author(s) 2018 Open 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/. |
spellingShingle | Article Niarchou, Maria Chawner, Samuel J. R. A. Doherty, Joanne L. Maillard, Anne M. Jacquemont, Sébastien Chung, Wendy K. Green-Snyder, LeeAnne Bernier, Raphael A. Goin-Kochel, Robin P. Hanson, Ellen Linden, David E. J. Linden, Stefanie C. Raymond, F. Lucy Skuse, David Hall, Jeremy Owen, Michael J. Bree, Marianne B. M. van den Psychiatric disorders in children with 16p11.2 deletion and duplication |
title | Psychiatric disorders in children with 16p11.2 deletion and duplication |
title_full | Psychiatric disorders in children with 16p11.2 deletion and duplication |
title_fullStr | Psychiatric disorders in children with 16p11.2 deletion and duplication |
title_full_unstemmed | Psychiatric disorders in children with 16p11.2 deletion and duplication |
title_short | Psychiatric disorders in children with 16p11.2 deletion and duplication |
title_sort | psychiatric disorders in children with 16p11.2 deletion and duplication |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341088/ https://www.ncbi.nlm.nih.gov/pubmed/30664628 http://dx.doi.org/10.1038/s41398-018-0339-8 |
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