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Femoral geometry, bone mineral density, and the risk of hip fracture in premenopausal women: a case control study

BACKGROUND: The purpose of this study was to determine the relationships among hip geometry, bone mineral density, and the risk of hip fracture in premenopausal women. METHODS: The participants in this case–control study were 16 premenopausal women with minimal-trauma hip fractures (fracture group)...

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Autores principales: Lee, Dong-Hwa, Jung, Kyong Yeun, Hong, A Ram, Kim, Jung Hee, Kim, Kyoung Min, Shin, Chan Soo, Kim, Seong Yeon, Kim, Sang Wan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727305/
https://www.ncbi.nlm.nih.gov/pubmed/26809738
http://dx.doi.org/10.1186/s12891-016-0893-2
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author Lee, Dong-Hwa
Jung, Kyong Yeun
Hong, A Ram
Kim, Jung Hee
Kim, Kyoung Min
Shin, Chan Soo
Kim, Seong Yeon
Kim, Sang Wan
author_facet Lee, Dong-Hwa
Jung, Kyong Yeun
Hong, A Ram
Kim, Jung Hee
Kim, Kyoung Min
Shin, Chan Soo
Kim, Seong Yeon
Kim, Sang Wan
author_sort Lee, Dong-Hwa
collection PubMed
description BACKGROUND: The purpose of this study was to determine the relationships among hip geometry, bone mineral density, and the risk of hip fracture in premenopausal women. METHODS: The participants in this case–control study were 16 premenopausal women with minimal-trauma hip fractures (fracture group) and 80 age-and BMI-adjusted controls. Subjects underwent dual-energy X-ray absorptiometry (DXA) to assess BMD at the proximal femur and to obtain DXA-derived hip geometry measurements. RESULTS: The fracture group had a lower mean femoral neck and total hip BMD than the control group (0.721 ± 0.123 vs. 0.899 ± 0.115, p <0.001 for the femoral neck BMD and 0.724 ± 0.120 vs. 0.923 ± 0.116, p <0.001 for the total hip BMD). In addition, participants in the fracture group had a longer hip axis length (HAL; p = 0.007), narrower neck shaft angle (NSA; p = 0.008), smaller cross sectional area (CSA; p < 0.001) and higher cross sectional moment of inertia (CSMI; p = 0.004) than those in control group. After adjusting for BMD, the fracture group still had a significantly longer mean HAL (p = 0.020) and narrower NSA (p = 0.006) than the control group. CONCLUSIONS: BMD is an important predictor of hip fracture in premenopausal women. Furthermore, HAL and NSA are BMD-independent predictors of hip fracture in premenopausal women. Hip geometry may be clinically useful for identification of premenopausal women for whom active fracture prevention should be considered.
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spelling pubmed-47273052016-01-27 Femoral geometry, bone mineral density, and the risk of hip fracture in premenopausal women: a case control study Lee, Dong-Hwa Jung, Kyong Yeun Hong, A Ram Kim, Jung Hee Kim, Kyoung Min Shin, Chan Soo Kim, Seong Yeon Kim, Sang Wan BMC Musculoskelet Disord Research Article BACKGROUND: The purpose of this study was to determine the relationships among hip geometry, bone mineral density, and the risk of hip fracture in premenopausal women. METHODS: The participants in this case–control study were 16 premenopausal women with minimal-trauma hip fractures (fracture group) and 80 age-and BMI-adjusted controls. Subjects underwent dual-energy X-ray absorptiometry (DXA) to assess BMD at the proximal femur and to obtain DXA-derived hip geometry measurements. RESULTS: The fracture group had a lower mean femoral neck and total hip BMD than the control group (0.721 ± 0.123 vs. 0.899 ± 0.115, p <0.001 for the femoral neck BMD and 0.724 ± 0.120 vs. 0.923 ± 0.116, p <0.001 for the total hip BMD). In addition, participants in the fracture group had a longer hip axis length (HAL; p = 0.007), narrower neck shaft angle (NSA; p = 0.008), smaller cross sectional area (CSA; p < 0.001) and higher cross sectional moment of inertia (CSMI; p = 0.004) than those in control group. After adjusting for BMD, the fracture group still had a significantly longer mean HAL (p = 0.020) and narrower NSA (p = 0.006) than the control group. CONCLUSIONS: BMD is an important predictor of hip fracture in premenopausal women. Furthermore, HAL and NSA are BMD-independent predictors of hip fracture in premenopausal women. Hip geometry may be clinically useful for identification of premenopausal women for whom active fracture prevention should be considered. BioMed Central 2016-01-25 /pmc/articles/PMC4727305/ /pubmed/26809738 http://dx.doi.org/10.1186/s12891-016-0893-2 Text en © Lee et al. 2016 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
Lee, Dong-Hwa
Jung, Kyong Yeun
Hong, A Ram
Kim, Jung Hee
Kim, Kyoung Min
Shin, Chan Soo
Kim, Seong Yeon
Kim, Sang Wan
Femoral geometry, bone mineral density, and the risk of hip fracture in premenopausal women: a case control study
title Femoral geometry, bone mineral density, and the risk of hip fracture in premenopausal women: a case control study
title_full Femoral geometry, bone mineral density, and the risk of hip fracture in premenopausal women: a case control study
title_fullStr Femoral geometry, bone mineral density, and the risk of hip fracture in premenopausal women: a case control study
title_full_unstemmed Femoral geometry, bone mineral density, and the risk of hip fracture in premenopausal women: a case control study
title_short Femoral geometry, bone mineral density, and the risk of hip fracture in premenopausal women: a case control study
title_sort femoral geometry, bone mineral density, and the risk of hip fracture in premenopausal women: a case control study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727305/
https://www.ncbi.nlm.nih.gov/pubmed/26809738
http://dx.doi.org/10.1186/s12891-016-0893-2
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