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Age-Related Changes in Femoral Head Trabecular Microarchitecture
Osteoporosis is a prevalent bone condition, characterised by low bone mineral density and increased fracture risk. Currently, the gold standard for identifying osteoporosis and increased fracture risk is through quantification of bone mineral density using dual energy X-ray absorption. However, many...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
JKL International LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6284768/ https://www.ncbi.nlm.nih.gov/pubmed/30574411 http://dx.doi.org/10.14336/AD.2018.0124 |
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author | Greenwood, Charlene Clement, John Dicken, Anthony Evans, Paul Lyburn, Iain Martin, Richard M. Stone, Nick Zioupos, Peter Rogers, Keith |
author_facet | Greenwood, Charlene Clement, John Dicken, Anthony Evans, Paul Lyburn, Iain Martin, Richard M. Stone, Nick Zioupos, Peter Rogers, Keith |
author_sort | Greenwood, Charlene |
collection | PubMed |
description | Osteoporosis is a prevalent bone condition, characterised by low bone mineral density and increased fracture risk. Currently, the gold standard for identifying osteoporosis and increased fracture risk is through quantification of bone mineral density using dual energy X-ray absorption. However, many studies have shown that bone strength, and consequently the probability of fracture, is a combination of both bone mass and bone ‘quality’ (architecture and material chemistry). Although the microarchitecture of both non-fracture and osteoporotic bone has been previously investigated, many of the osteoporotic studies are constrained by factors such as limited sample number, use of ovariectomised animal models, and lack of male and female discrimination. This study reports significant differences in bone quality with respect to the microarchitecture between fractured and non-fractured human femur specimens. Micro-computed tomography was utilised to investigate the microarchitecture of femoral head trabecular bone from a relatively large cohort of non-fracture and fracture human donors. Various microarchitectural parameters have been determined for both groups, providing an understanding of the differences between fracture and non -fracture material. The microarchitecture of non-fracture and fracture bone tissue is shown to be significantly different for many parameters. Differences between sexes also exist, suggesting differences in remodelling between males and females in the fracture group. The results from this study will, in the future, be applied to develop a fracture model which encompasses bone density, architecture and material chemical properties for both female and male tissues. |
format | Online Article Text |
id | pubmed-6284768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | JKL International LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-62847682018-12-20 Age-Related Changes in Femoral Head Trabecular Microarchitecture Greenwood, Charlene Clement, John Dicken, Anthony Evans, Paul Lyburn, Iain Martin, Richard M. Stone, Nick Zioupos, Peter Rogers, Keith Aging Dis Orginal Article Osteoporosis is a prevalent bone condition, characterised by low bone mineral density and increased fracture risk. Currently, the gold standard for identifying osteoporosis and increased fracture risk is through quantification of bone mineral density using dual energy X-ray absorption. However, many studies have shown that bone strength, and consequently the probability of fracture, is a combination of both bone mass and bone ‘quality’ (architecture and material chemistry). Although the microarchitecture of both non-fracture and osteoporotic bone has been previously investigated, many of the osteoporotic studies are constrained by factors such as limited sample number, use of ovariectomised animal models, and lack of male and female discrimination. This study reports significant differences in bone quality with respect to the microarchitecture between fractured and non-fractured human femur specimens. Micro-computed tomography was utilised to investigate the microarchitecture of femoral head trabecular bone from a relatively large cohort of non-fracture and fracture human donors. Various microarchitectural parameters have been determined for both groups, providing an understanding of the differences between fracture and non -fracture material. The microarchitecture of non-fracture and fracture bone tissue is shown to be significantly different for many parameters. Differences between sexes also exist, suggesting differences in remodelling between males and females in the fracture group. The results from this study will, in the future, be applied to develop a fracture model which encompasses bone density, architecture and material chemical properties for both female and male tissues. JKL International LLC 2018-12-04 /pmc/articles/PMC6284768/ /pubmed/30574411 http://dx.doi.org/10.14336/AD.2018.0124 Text en Copyright: © 2018 Charlene et al. http://creativecommons.org/licenses/by/2.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Orginal Article Greenwood, Charlene Clement, John Dicken, Anthony Evans, Paul Lyburn, Iain Martin, Richard M. Stone, Nick Zioupos, Peter Rogers, Keith Age-Related Changes in Femoral Head Trabecular Microarchitecture |
title | Age-Related Changes in Femoral Head Trabecular Microarchitecture |
title_full | Age-Related Changes in Femoral Head Trabecular Microarchitecture |
title_fullStr | Age-Related Changes in Femoral Head Trabecular Microarchitecture |
title_full_unstemmed | Age-Related Changes in Femoral Head Trabecular Microarchitecture |
title_short | Age-Related Changes in Femoral Head Trabecular Microarchitecture |
title_sort | age-related changes in femoral head trabecular microarchitecture |
topic | Orginal Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6284768/ https://www.ncbi.nlm.nih.gov/pubmed/30574411 http://dx.doi.org/10.14336/AD.2018.0124 |
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