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Child and adult adiposity and subtype-specific endometrial cancer risk: a multivariable Mendelian randomisation study
Increased adiposity is a known risk factor for endometrial cancer (EC). This study aimed to disentangle the separate causal roles of child and adult adiposity on EC risk in adults, including endometrioid and non-endometrioid histological subtypes using multivariable Mendelian randomisation. These an...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834041/ https://www.ncbi.nlm.nih.gov/pubmed/36357562 http://dx.doi.org/10.1038/s41366-022-01231-y |
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author | Kennedy, Oliver J. Bafligil, Cemsel O’Mara, Tracy A. Wang, Xuemin Evans, D. Gareth Kar, Siddhartha Crosbie, Emma J. |
author_facet | Kennedy, Oliver J. Bafligil, Cemsel O’Mara, Tracy A. Wang, Xuemin Evans, D. Gareth Kar, Siddhartha Crosbie, Emma J. |
author_sort | Kennedy, Oliver J. |
collection | PubMed |
description | Increased adiposity is a known risk factor for endometrial cancer (EC). This study aimed to disentangle the separate causal roles of child and adult adiposity on EC risk in adults, including endometrioid and non-endometrioid histological subtypes using multivariable Mendelian randomisation. These analyses employed genetic associations derived from UK Biobank as proxies for child and adult body size in 12,906 cases and 108,979 controls that participated in the Endometrial Cancer Association Consortium. In multivariable analyses, adult body size increased overall EC (OR 2.30, 95% CI 1.73–3.06) and endometrioid EC risk (OR 2.28, 95% CI 1.65–3.16), while child body size had minimal effect. In contrast, child body size (OR 2.26, 95% CI 1.03–4.99) but not adult body size increased non-endometrioid EC risk. As such, child adiposity has an indirect effect on endometrioid EC risk that is mediated by adult adiposity but has a direct effect on non-endometrioid EC risk that is independent of adult adiposity. These novel findings indicate that interventions targeting adiposity during distinct periods in life have a critical role in preventing subtype-specific EC. |
format | Online Article Text |
id | pubmed-9834041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98340412023-01-13 Child and adult adiposity and subtype-specific endometrial cancer risk: a multivariable Mendelian randomisation study Kennedy, Oliver J. Bafligil, Cemsel O’Mara, Tracy A. Wang, Xuemin Evans, D. Gareth Kar, Siddhartha Crosbie, Emma J. Int J Obes (Lond) Brief Communication Increased adiposity is a known risk factor for endometrial cancer (EC). This study aimed to disentangle the separate causal roles of child and adult adiposity on EC risk in adults, including endometrioid and non-endometrioid histological subtypes using multivariable Mendelian randomisation. These analyses employed genetic associations derived from UK Biobank as proxies for child and adult body size in 12,906 cases and 108,979 controls that participated in the Endometrial Cancer Association Consortium. In multivariable analyses, adult body size increased overall EC (OR 2.30, 95% CI 1.73–3.06) and endometrioid EC risk (OR 2.28, 95% CI 1.65–3.16), while child body size had minimal effect. In contrast, child body size (OR 2.26, 95% CI 1.03–4.99) but not adult body size increased non-endometrioid EC risk. As such, child adiposity has an indirect effect on endometrioid EC risk that is mediated by adult adiposity but has a direct effect on non-endometrioid EC risk that is independent of adult adiposity. These novel findings indicate that interventions targeting adiposity during distinct periods in life have a critical role in preventing subtype-specific EC. Nature Publishing Group UK 2022-11-10 2023 /pmc/articles/PMC9834041/ /pubmed/36357562 http://dx.doi.org/10.1038/s41366-022-01231-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Brief Communication Kennedy, Oliver J. Bafligil, Cemsel O’Mara, Tracy A. Wang, Xuemin Evans, D. Gareth Kar, Siddhartha Crosbie, Emma J. Child and adult adiposity and subtype-specific endometrial cancer risk: a multivariable Mendelian randomisation study |
title | Child and adult adiposity and subtype-specific endometrial cancer risk: a multivariable Mendelian randomisation study |
title_full | Child and adult adiposity and subtype-specific endometrial cancer risk: a multivariable Mendelian randomisation study |
title_fullStr | Child and adult adiposity and subtype-specific endometrial cancer risk: a multivariable Mendelian randomisation study |
title_full_unstemmed | Child and adult adiposity and subtype-specific endometrial cancer risk: a multivariable Mendelian randomisation study |
title_short | Child and adult adiposity and subtype-specific endometrial cancer risk: a multivariable Mendelian randomisation study |
title_sort | child and adult adiposity and subtype-specific endometrial cancer risk: a multivariable mendelian randomisation study |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834041/ https://www.ncbi.nlm.nih.gov/pubmed/36357562 http://dx.doi.org/10.1038/s41366-022-01231-y |
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