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BMD-Related Genetic Risk Scores Predict Site-Specific Fractures as Well as Trabecular and Cortical Bone Microstructure
CONTEXT: It is important to identify patients at highest risk of fractures. OBJECTIVE: To compare the separate and combined performances of bone-related genetic risk scores (GRSs) for prediction of forearm, hip and vertebral fractures separately, as well as of trabecular and cortical bone microstruc...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069346/ https://www.ncbi.nlm.nih.gov/pubmed/32067027 http://dx.doi.org/10.1210/clinem/dgaa082 |
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author | Nethander, Maria Pettersson-Kymmer, Ulrika Vandenput, Liesbeth Lorentzon, Mattias Karlsson, Magnus Mellström, Dan Ohlsson, Claes |
author_facet | Nethander, Maria Pettersson-Kymmer, Ulrika Vandenput, Liesbeth Lorentzon, Mattias Karlsson, Magnus Mellström, Dan Ohlsson, Claes |
author_sort | Nethander, Maria |
collection | PubMed |
description | CONTEXT: It is important to identify patients at highest risk of fractures. OBJECTIVE: To compare the separate and combined performances of bone-related genetic risk scores (GRSs) for prediction of forearm, hip and vertebral fractures separately, as well as of trabecular and cortical bone microstructure parameters separately. DESIGN, SETTING, AND PARTICIPANTS: Using 1103 single nucleotide polymorphisms (SNPs) independently associated with estimated bone mineral density of the heel (eBMD), we developed a weighted GRS for eBMD and determined its contribution to fracture prediction beyond 2 previously developed GRSs for femur neck BMD (49 SNPs) and lumbar spine BMD (48 SNPs). Associations between these GRSs and forearm (n(cases) = 1020; n(controls) = 2838), hip (n(cases) = 1123; n(controls) = 2630) and vertebral (n(cases) = 288; n(controls) = 1187) fractures were evaluated in 3 Swedish cohorts. Associations between the GRSs and trabecular and cortical bone microstructure parameters (n = 426) were evaluated in the MrOS Sweden cohort. RESULTS: We found that eBMD(GRS) was the only significant independent predictor of forearm and vertebral fractures while both FN-BMD(GRS) and eBMD(GRS) were significant independent predictors of hip fractures. The eBMD(GRS) was the major GRS contributing to prediction of trabecular bone microstructure parameters while both FN-BMD(GRS) and eBMD(GRS) contributed information for prediction of cortical bone microstructure parameters. CONCLUSIONS: The eBMD(GRS) independently predicts forearm and vertebral fractures while both FN-BMD(GRS) and eBMD(GRS) contribute independent information for prediction of hip fractures. We propose that eBMD(GRS) captures unique information about trabecular bone microstructure useful for prediction of forearm and vertebral fractures. These findings may facilitate personalized medicine to predict site-specific fractures as well as cortical and trabecular bone microstructure separately. |
format | Online Article Text |
id | pubmed-7069346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70693462020-03-18 BMD-Related Genetic Risk Scores Predict Site-Specific Fractures as Well as Trabecular and Cortical Bone Microstructure Nethander, Maria Pettersson-Kymmer, Ulrika Vandenput, Liesbeth Lorentzon, Mattias Karlsson, Magnus Mellström, Dan Ohlsson, Claes J Clin Endocrinol Metab Online Only Articles CONTEXT: It is important to identify patients at highest risk of fractures. OBJECTIVE: To compare the separate and combined performances of bone-related genetic risk scores (GRSs) for prediction of forearm, hip and vertebral fractures separately, as well as of trabecular and cortical bone microstructure parameters separately. DESIGN, SETTING, AND PARTICIPANTS: Using 1103 single nucleotide polymorphisms (SNPs) independently associated with estimated bone mineral density of the heel (eBMD), we developed a weighted GRS for eBMD and determined its contribution to fracture prediction beyond 2 previously developed GRSs for femur neck BMD (49 SNPs) and lumbar spine BMD (48 SNPs). Associations between these GRSs and forearm (n(cases) = 1020; n(controls) = 2838), hip (n(cases) = 1123; n(controls) = 2630) and vertebral (n(cases) = 288; n(controls) = 1187) fractures were evaluated in 3 Swedish cohorts. Associations between the GRSs and trabecular and cortical bone microstructure parameters (n = 426) were evaluated in the MrOS Sweden cohort. RESULTS: We found that eBMD(GRS) was the only significant independent predictor of forearm and vertebral fractures while both FN-BMD(GRS) and eBMD(GRS) were significant independent predictors of hip fractures. The eBMD(GRS) was the major GRS contributing to prediction of trabecular bone microstructure parameters while both FN-BMD(GRS) and eBMD(GRS) contributed information for prediction of cortical bone microstructure parameters. CONCLUSIONS: The eBMD(GRS) independently predicts forearm and vertebral fractures while both FN-BMD(GRS) and eBMD(GRS) contribute independent information for prediction of hip fractures. We propose that eBMD(GRS) captures unique information about trabecular bone microstructure useful for prediction of forearm and vertebral fractures. These findings may facilitate personalized medicine to predict site-specific fractures as well as cortical and trabecular bone microstructure separately. Oxford University Press 2020-02-18 /pmc/articles/PMC7069346/ /pubmed/32067027 http://dx.doi.org/10.1210/clinem/dgaa082 Text en © Endocrine Society 2020. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Online Only Articles Nethander, Maria Pettersson-Kymmer, Ulrika Vandenput, Liesbeth Lorentzon, Mattias Karlsson, Magnus Mellström, Dan Ohlsson, Claes BMD-Related Genetic Risk Scores Predict Site-Specific Fractures as Well as Trabecular and Cortical Bone Microstructure |
title | BMD-Related Genetic Risk Scores Predict Site-Specific Fractures as Well as Trabecular and Cortical Bone Microstructure |
title_full | BMD-Related Genetic Risk Scores Predict Site-Specific Fractures as Well as Trabecular and Cortical Bone Microstructure |
title_fullStr | BMD-Related Genetic Risk Scores Predict Site-Specific Fractures as Well as Trabecular and Cortical Bone Microstructure |
title_full_unstemmed | BMD-Related Genetic Risk Scores Predict Site-Specific Fractures as Well as Trabecular and Cortical Bone Microstructure |
title_short | BMD-Related Genetic Risk Scores Predict Site-Specific Fractures as Well as Trabecular and Cortical Bone Microstructure |
title_sort | bmd-related genetic risk scores predict site-specific fractures as well as trabecular and cortical bone microstructure |
topic | Online Only Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069346/ https://www.ncbi.nlm.nih.gov/pubmed/32067027 http://dx.doi.org/10.1210/clinem/dgaa082 |
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