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Age-specific effects of weight-based body size on fracture risk in later life: a lifecourse Mendelian randomisation study

Musculoskeletal conditions, including fractures, can have severe and long-lasting consequences. Higher body mass index in adulthood is widely acknowledged to be protective for most fracture sites. However, sources of bias induced by confounding factors may have distorted previous findings. Employing...

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Autores principales: Power, Grace Marion, Tobias, Jonathan H, Frayling, Timothy M, Tyrrell, Jessica, Hartley, April E, Heron, Jon E, Davey Smith, George, Richardson, Tom G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276076/
https://www.ncbi.nlm.nih.gov/pubmed/37133737
http://dx.doi.org/10.1007/s10654-023-00986-6
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author Power, Grace Marion
Tobias, Jonathan H
Frayling, Timothy M
Tyrrell, Jessica
Hartley, April E
Heron, Jon E
Davey Smith, George
Richardson, Tom G
author_facet Power, Grace Marion
Tobias, Jonathan H
Frayling, Timothy M
Tyrrell, Jessica
Hartley, April E
Heron, Jon E
Davey Smith, George
Richardson, Tom G
author_sort Power, Grace Marion
collection PubMed
description Musculoskeletal conditions, including fractures, can have severe and long-lasting consequences. Higher body mass index in adulthood is widely acknowledged to be protective for most fracture sites. However, sources of bias induced by confounding factors may have distorted previous findings. Employing a lifecourse Mendelian randomisation (MR) approach by using genetic instruments to separate effects at different life stages, this investigation aims to explore how prepubertal and adult body size independently influence fracture risk in later life. Using data from a large prospective cohort, univariable and multivariable MR were conducted to simultaneously estimate the effects of age-specific genetic proxies for body size (n = 453,169) on fracture risk (n = 416,795). A two-step MR framework was additionally applied to elucidate potential mediators. Univariable and multivariable MR indicated strong evidence that higher body size in childhood reduced fracture risk (OR, 95% CI: 0.89, 0.82 to 0.96, P = 0.005 and 0.76, 0.69 to 0.85, P = 1 × 10(− 6), respectively). Conversely, higher body size in adulthood increased fracture risk (OR, 95% CI: 1.08, 1.01 to 1.16, P = 0.023 and 1.26, 1.14 to 1.38, P = 2 × 10(− 6), respectively). Two-step MR analyses suggested that the effect of higher body size in childhood on reduced fracture risk was mediated by its influence on higher estimated bone mineral density (eBMD) in adulthood. This investigation provides novel evidence that higher body size in childhood reduces fracture risk in later life through its influence on increased eBMD. From a public health perspective, this relationship is complex since obesity in adulthood remains a major risk factor for co-morbidities. Results additionally indicate that higher body size in adulthood is a risk factor for fractures. Protective effect estimates previously observed are likely attributed to childhood effects. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10654-023-00986-6.
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spelling pubmed-102760762023-06-18 Age-specific effects of weight-based body size on fracture risk in later life: a lifecourse Mendelian randomisation study Power, Grace Marion Tobias, Jonathan H Frayling, Timothy M Tyrrell, Jessica Hartley, April E Heron, Jon E Davey Smith, George Richardson, Tom G Eur J Epidemiol Locomotor Diseases Musculoskeletal conditions, including fractures, can have severe and long-lasting consequences. Higher body mass index in adulthood is widely acknowledged to be protective for most fracture sites. However, sources of bias induced by confounding factors may have distorted previous findings. Employing a lifecourse Mendelian randomisation (MR) approach by using genetic instruments to separate effects at different life stages, this investigation aims to explore how prepubertal and adult body size independently influence fracture risk in later life. Using data from a large prospective cohort, univariable and multivariable MR were conducted to simultaneously estimate the effects of age-specific genetic proxies for body size (n = 453,169) on fracture risk (n = 416,795). A two-step MR framework was additionally applied to elucidate potential mediators. Univariable and multivariable MR indicated strong evidence that higher body size in childhood reduced fracture risk (OR, 95% CI: 0.89, 0.82 to 0.96, P = 0.005 and 0.76, 0.69 to 0.85, P = 1 × 10(− 6), respectively). Conversely, higher body size in adulthood increased fracture risk (OR, 95% CI: 1.08, 1.01 to 1.16, P = 0.023 and 1.26, 1.14 to 1.38, P = 2 × 10(− 6), respectively). Two-step MR analyses suggested that the effect of higher body size in childhood on reduced fracture risk was mediated by its influence on higher estimated bone mineral density (eBMD) in adulthood. This investigation provides novel evidence that higher body size in childhood reduces fracture risk in later life through its influence on increased eBMD. From a public health perspective, this relationship is complex since obesity in adulthood remains a major risk factor for co-morbidities. Results additionally indicate that higher body size in adulthood is a risk factor for fractures. Protective effect estimates previously observed are likely attributed to childhood effects. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10654-023-00986-6. Springer Netherlands 2023-05-03 2023 /pmc/articles/PMC10276076/ /pubmed/37133737 http://dx.doi.org/10.1007/s10654-023-00986-6 Text en © The Author(s) 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Locomotor Diseases
Power, Grace Marion
Tobias, Jonathan H
Frayling, Timothy M
Tyrrell, Jessica
Hartley, April E
Heron, Jon E
Davey Smith, George
Richardson, Tom G
Age-specific effects of weight-based body size on fracture risk in later life: a lifecourse Mendelian randomisation study
title Age-specific effects of weight-based body size on fracture risk in later life: a lifecourse Mendelian randomisation study
title_full Age-specific effects of weight-based body size on fracture risk in later life: a lifecourse Mendelian randomisation study
title_fullStr Age-specific effects of weight-based body size on fracture risk in later life: a lifecourse Mendelian randomisation study
title_full_unstemmed Age-specific effects of weight-based body size on fracture risk in later life: a lifecourse Mendelian randomisation study
title_short Age-specific effects of weight-based body size on fracture risk in later life: a lifecourse Mendelian randomisation study
title_sort age-specific effects of weight-based body size on fracture risk in later life: a lifecourse mendelian randomisation study
topic Locomotor Diseases
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276076/
https://www.ncbi.nlm.nih.gov/pubmed/37133737
http://dx.doi.org/10.1007/s10654-023-00986-6
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