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Effects of pathogenic CNVs on physical traits in participants of the UK Biobank
BACKGROUND: Copy number variants (CNVs) have been shown to increase risk for physical anomalies, developmental, psychiatric and medical disorders. Some of them have been associated with changes in weight, height, and other physical traits. As most studies have been performed on children and young pe...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278042/ https://www.ncbi.nlm.nih.gov/pubmed/30509170 http://dx.doi.org/10.1186/s12864-018-5292-7 |
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author | Owen, David Bracher-Smith, Mathew Kendall, Kimberley M. Rees, Elliott Einon, Mark Escott-Price, Valentina Owen, Michael J. O’Donovan, Michael C. Kirov, George |
author_facet | Owen, David Bracher-Smith, Mathew Kendall, Kimberley M. Rees, Elliott Einon, Mark Escott-Price, Valentina Owen, Michael J. O’Donovan, Michael C. Kirov, George |
author_sort | Owen, David |
collection | PubMed |
description | BACKGROUND: Copy number variants (CNVs) have been shown to increase risk for physical anomalies, developmental, psychiatric and medical disorders. Some of them have been associated with changes in weight, height, and other physical traits. As most studies have been performed on children and young people, these effects of CNVs in middle-aged and older people are not well established. The UK Biobank recruited half a million adults who provided a variety of physical measurements. We called all CNVs from the Affymetrix microarrays and selected a set of 54 CNVs implicated as pathogenic (including their reciprocal deletions/duplications) and that were found in five or more persons. Linear regression analysis was used to establish their association with 16 physical traits relevant to human health. RESULTS: 396,725 participants of white British or Irish descent (excluding first-degree relatives) passed our quality control filters. Out of the 864 CNV/trait associations, 214 were significant at a false discovery rate of 0.1, most of them novel. Many of these traits increase risk for adverse health outcomes: e.g. increases in weight, waist-to-hip ratio, pulse rate and body fat composition. Deletions at 16p11.2, 16p12.1, NRXN1 and duplications at 16p13.11 and 22q11.2 produced the highest numbers of significant associations. Five CNVs produced average changes of over one standard deviation for the 16 traits, compared to controls: deletions at 16p11.2 and 22q11.2, and duplications at 3q29, the Williams-Beuren and Potocki-Lupski regions. CNVs at 1q21.1, 2q13, 16p11.2 and 16p11.2 distal, 16p12.1, 17p12 and 17q12 demonstrated one or more mirror image effects of deletions versus duplications. CONCLUSIONS: Carriers of many CNVs should be monitored for physical traits that increase morbidity and mortality. Genes within these CNVs can give insights into biological processes and therapeutic interventions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5292-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6278042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62780422018-12-06 Effects of pathogenic CNVs on physical traits in participants of the UK Biobank Owen, David Bracher-Smith, Mathew Kendall, Kimberley M. Rees, Elliott Einon, Mark Escott-Price, Valentina Owen, Michael J. O’Donovan, Michael C. Kirov, George BMC Genomics Research Article BACKGROUND: Copy number variants (CNVs) have been shown to increase risk for physical anomalies, developmental, psychiatric and medical disorders. Some of them have been associated with changes in weight, height, and other physical traits. As most studies have been performed on children and young people, these effects of CNVs in middle-aged and older people are not well established. The UK Biobank recruited half a million adults who provided a variety of physical measurements. We called all CNVs from the Affymetrix microarrays and selected a set of 54 CNVs implicated as pathogenic (including their reciprocal deletions/duplications) and that were found in five or more persons. Linear regression analysis was used to establish their association with 16 physical traits relevant to human health. RESULTS: 396,725 participants of white British or Irish descent (excluding first-degree relatives) passed our quality control filters. Out of the 864 CNV/trait associations, 214 were significant at a false discovery rate of 0.1, most of them novel. Many of these traits increase risk for adverse health outcomes: e.g. increases in weight, waist-to-hip ratio, pulse rate and body fat composition. Deletions at 16p11.2, 16p12.1, NRXN1 and duplications at 16p13.11 and 22q11.2 produced the highest numbers of significant associations. Five CNVs produced average changes of over one standard deviation for the 16 traits, compared to controls: deletions at 16p11.2 and 22q11.2, and duplications at 3q29, the Williams-Beuren and Potocki-Lupski regions. CNVs at 1q21.1, 2q13, 16p11.2 and 16p11.2 distal, 16p12.1, 17p12 and 17q12 demonstrated one or more mirror image effects of deletions versus duplications. CONCLUSIONS: Carriers of many CNVs should be monitored for physical traits that increase morbidity and mortality. Genes within these CNVs can give insights into biological processes and therapeutic interventions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5292-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-04 /pmc/articles/PMC6278042/ /pubmed/30509170 http://dx.doi.org/10.1186/s12864-018-5292-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Owen, David Bracher-Smith, Mathew Kendall, Kimberley M. Rees, Elliott Einon, Mark Escott-Price, Valentina Owen, Michael J. O’Donovan, Michael C. Kirov, George Effects of pathogenic CNVs on physical traits in participants of the UK Biobank |
title | Effects of pathogenic CNVs on physical traits in participants of the UK Biobank |
title_full | Effects of pathogenic CNVs on physical traits in participants of the UK Biobank |
title_fullStr | Effects of pathogenic CNVs on physical traits in participants of the UK Biobank |
title_full_unstemmed | Effects of pathogenic CNVs on physical traits in participants of the UK Biobank |
title_short | Effects of pathogenic CNVs on physical traits in participants of the UK Biobank |
title_sort | effects of pathogenic cnvs on physical traits in participants of the uk biobank |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278042/ https://www.ncbi.nlm.nih.gov/pubmed/30509170 http://dx.doi.org/10.1186/s12864-018-5292-7 |
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