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Associations between Body Composition, Hormonal and Lifestyle Factors, Bone Turnover, and BMD

BACKGROUND: The relative importance of body composition, lifestyle factors, bone turnover and hormonal factors in determining bone mineral density (BMD) is unknown. We studied younger postmenopausal women to determine whether modifiable or nonmodifiable risk factors for osteoporosis have stronger as...

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Autores principales: Gourlay, Margaret L., Hammett-Stabler, Catherine A., Renner, Jordan B., Rubin, Janet E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Bone and Mineral Research 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3970292/
https://www.ncbi.nlm.nih.gov/pubmed/24707468
http://dx.doi.org/10.11005/jbm.2014.21.1.61
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author Gourlay, Margaret L.
Hammett-Stabler, Catherine A.
Renner, Jordan B.
Rubin, Janet E.
author_facet Gourlay, Margaret L.
Hammett-Stabler, Catherine A.
Renner, Jordan B.
Rubin, Janet E.
author_sort Gourlay, Margaret L.
collection PubMed
description BACKGROUND: The relative importance of body composition, lifestyle factors, bone turnover and hormonal factors in determining bone mineral density (BMD) is unknown. We studied younger postmenopausal women to determine whether modifiable or nonmodifiable risk factors for osteoporosis have stronger associations with BMD. METHODS: In multivariable linear regression models, we tested associations between non-bone body composition measures, self-reported measures of physical activity and dietary intake, urinary N-telopeptide (NTx), sex hormone concentrations, and BMD in 109 postmenopausal women aged 50 to 64 years, adjusting for current hormone therapy use and clinical risk factors for low BMD. Lean mass, fat mass and areal BMD (aBMD) at the lumbar spine, femoral neck, total hip and distal radius were measured using dual energy X-ray absorptiometry. RESULTS: Higher body weight and self-reported nonwhite race were independently associated with higher aBMD at the lumbar spine, femoral neck, total hip and distal radius. Lean and fat mass were not independently associated with aBMD. Older age and higher urinary NTx were independently associated with lower aBMD at the distal radius but not at weight-bearing sites. Sensitivity analyses demonstrated lack of an independent association between total daily protein or calorie intake and BMD. CONCLUSIONS: BMD, weight and race were the most important determinants of aBMD at all sites. Older age and higher bone turnover were independently associated with lower aBMD at the distal radius. In a limited analysis, self-reported physical activity, dietary protein and calorie intake were not associated with aBMD after adjustment for the other variables.
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spelling pubmed-39702922014-04-04 Associations between Body Composition, Hormonal and Lifestyle Factors, Bone Turnover, and BMD Gourlay, Margaret L. Hammett-Stabler, Catherine A. Renner, Jordan B. Rubin, Janet E. J Bone Metab Original Article BACKGROUND: The relative importance of body composition, lifestyle factors, bone turnover and hormonal factors in determining bone mineral density (BMD) is unknown. We studied younger postmenopausal women to determine whether modifiable or nonmodifiable risk factors for osteoporosis have stronger associations with BMD. METHODS: In multivariable linear regression models, we tested associations between non-bone body composition measures, self-reported measures of physical activity and dietary intake, urinary N-telopeptide (NTx), sex hormone concentrations, and BMD in 109 postmenopausal women aged 50 to 64 years, adjusting for current hormone therapy use and clinical risk factors for low BMD. Lean mass, fat mass and areal BMD (aBMD) at the lumbar spine, femoral neck, total hip and distal radius were measured using dual energy X-ray absorptiometry. RESULTS: Higher body weight and self-reported nonwhite race were independently associated with higher aBMD at the lumbar spine, femoral neck, total hip and distal radius. Lean and fat mass were not independently associated with aBMD. Older age and higher urinary NTx were independently associated with lower aBMD at the distal radius but not at weight-bearing sites. Sensitivity analyses demonstrated lack of an independent association between total daily protein or calorie intake and BMD. CONCLUSIONS: BMD, weight and race were the most important determinants of aBMD at all sites. Older age and higher bone turnover were independently associated with lower aBMD at the distal radius. In a limited analysis, self-reported physical activity, dietary protein and calorie intake were not associated with aBMD after adjustment for the other variables. The Korean Society for Bone and Mineral Research 2014-02 2014-02-28 /pmc/articles/PMC3970292/ /pubmed/24707468 http://dx.doi.org/10.11005/jbm.2014.21.1.61 Text en Copyright © 2014 The Korean Society for Bone and Mineral Research http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Gourlay, Margaret L.
Hammett-Stabler, Catherine A.
Renner, Jordan B.
Rubin, Janet E.
Associations between Body Composition, Hormonal and Lifestyle Factors, Bone Turnover, and BMD
title Associations between Body Composition, Hormonal and Lifestyle Factors, Bone Turnover, and BMD
title_full Associations between Body Composition, Hormonal and Lifestyle Factors, Bone Turnover, and BMD
title_fullStr Associations between Body Composition, Hormonal and Lifestyle Factors, Bone Turnover, and BMD
title_full_unstemmed Associations between Body Composition, Hormonal and Lifestyle Factors, Bone Turnover, and BMD
title_short Associations between Body Composition, Hormonal and Lifestyle Factors, Bone Turnover, and BMD
title_sort associations between body composition, hormonal and lifestyle factors, bone turnover, and bmd
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3970292/
https://www.ncbi.nlm.nih.gov/pubmed/24707468
http://dx.doi.org/10.11005/jbm.2014.21.1.61
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