Effects of long-term alendronate treatment on bone mineralisation, resorption parameters and biomechanics of single human vertebral trabeculae

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Effects of long-term alendronate treatment on bone mineralisation, resorption parameters and biomechanics of single human vertebral trabeculae. / Krause, M; Soltau, Markus; Zimmermann, E A; Hahn, M; Kornet , Jacob Jan; Hapfelmeier, A; Breer, S; Morlock, M; Wulff, B; Püschel, K; Glueer, C-C; Amling, M; Busse, B.

in: EUR CELLS MATER, Jahrgang 28, 01.01.2014, S. 152-165.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Krause, M, Soltau, M, Zimmermann, EA, Hahn, M, Kornet , JJ, Hapfelmeier, A, Breer, S, Morlock, M, Wulff, B, Püschel, K, Glueer, C-C, Amling, M & Busse, B 2014, 'Effects of long-term alendronate treatment on bone mineralisation, resorption parameters and biomechanics of single human vertebral trabeculae', EUR CELLS MATER, Jg. 28, S. 152-165.

APA

Krause, M., Soltau, M., Zimmermann, E. A., Hahn, M., Kornet , J. J., Hapfelmeier, A., Breer, S., Morlock, M., Wulff, B., Püschel, K., Glueer, C-C., Amling, M., & Busse, B. (2014). Effects of long-term alendronate treatment on bone mineralisation, resorption parameters and biomechanics of single human vertebral trabeculae. EUR CELLS MATER, 28, 152-165.

Vancouver

Bibtex

@article{2043f08e5d164fcd88c96fa8492cdd58,
title = "Effects of long-term alendronate treatment on bone mineralisation, resorption parameters and biomechanics of single human vertebral trabeculae",
abstract = "Due to their well-established fracture risk reduction, bisphosphonates are the most frequently used therapeutic agent to treat osteoporosis. Bisphosphonates reduce fracture risk by suppressing bone resorption, but the lower bone turnover could have a negative impact on bone quality at the tissue level. Here, we directly assess the structural and mechanical characteristics of cancellous bone from the lumbar vertebrae (L5) in non-treated osteoporotic controls (n=21), mid-term alendronate-treated osteoporotic patients (n=6), and long-term alendronate-treated osteoporotic patients (n=7). The strength and toughness of single trabeculae were evaluated, while the structure was characterised through measurements of microdamage accumulation, mineralisation distribution, and histological indices. The alendronate-treated cases had a reduced eroded surface (ES/BS, p<0.001) and a higher bone mineralisation in comparison to non-treated controls (p=0.037), which is indicative of low turnover associated with treatment. However, the amount of microdamage and the mechanical properties were similar among the control and treatment groups. As the tissue mineral density (TMD) increased significantly with alendronate treatment compared to non-treated osteoporotic controls, the reduction in resorption cavities could counterbalance the higher TMD allowing the alendronate-treated bone to maintain its mechanical properties and resist microdamage accumulation. A multivariate analysis of the possible predictors supports the theory that multiple factors (e.g., body mass index, TMD, and ES/BS) can impact the mechanical properties. Our results suggest that long-term alendronate treatment shows no adverse impact on mechanical cancellous bone characteristics.",
keywords = "Aged, Aged, 80 and over, Alendronate, Biomechanical Phenomena, Bone Density Conservation Agents, Bone Resorption, Calcification, Physiologic, Female, Humans, Lumbar Vertebrae, Osteoporosis, Postmenopausal",
author = "M Krause and Markus Soltau and Zimmermann, {E A} and M Hahn and Kornet, {Jacob Jan} and A Hapfelmeier and S Breer and M Morlock and B Wulff and K P{\"u}schel and C-C Glueer and M Amling and B Busse",
year = "2014",
month = jan,
day = "1",
language = "English",
volume = "28",
pages = "152--165",
journal = "EUR CELLS MATER",
issn = "1473-2262",
publisher = "Swiss Society for Biomaterials",

}

RIS

TY - JOUR

T1 - Effects of long-term alendronate treatment on bone mineralisation, resorption parameters and biomechanics of single human vertebral trabeculae

AU - Krause, M

AU - Soltau, Markus

AU - Zimmermann, E A

AU - Hahn, M

AU - Kornet , Jacob Jan

AU - Hapfelmeier, A

AU - Breer, S

AU - Morlock, M

AU - Wulff, B

AU - Püschel, K

AU - Glueer, C-C

AU - Amling, M

AU - Busse, B

PY - 2014/1/1

Y1 - 2014/1/1

N2 - Due to their well-established fracture risk reduction, bisphosphonates are the most frequently used therapeutic agent to treat osteoporosis. Bisphosphonates reduce fracture risk by suppressing bone resorption, but the lower bone turnover could have a negative impact on bone quality at the tissue level. Here, we directly assess the structural and mechanical characteristics of cancellous bone from the lumbar vertebrae (L5) in non-treated osteoporotic controls (n=21), mid-term alendronate-treated osteoporotic patients (n=6), and long-term alendronate-treated osteoporotic patients (n=7). The strength and toughness of single trabeculae were evaluated, while the structure was characterised through measurements of microdamage accumulation, mineralisation distribution, and histological indices. The alendronate-treated cases had a reduced eroded surface (ES/BS, p<0.001) and a higher bone mineralisation in comparison to non-treated controls (p=0.037), which is indicative of low turnover associated with treatment. However, the amount of microdamage and the mechanical properties were similar among the control and treatment groups. As the tissue mineral density (TMD) increased significantly with alendronate treatment compared to non-treated osteoporotic controls, the reduction in resorption cavities could counterbalance the higher TMD allowing the alendronate-treated bone to maintain its mechanical properties and resist microdamage accumulation. A multivariate analysis of the possible predictors supports the theory that multiple factors (e.g., body mass index, TMD, and ES/BS) can impact the mechanical properties. Our results suggest that long-term alendronate treatment shows no adverse impact on mechanical cancellous bone characteristics.

AB - Due to their well-established fracture risk reduction, bisphosphonates are the most frequently used therapeutic agent to treat osteoporosis. Bisphosphonates reduce fracture risk by suppressing bone resorption, but the lower bone turnover could have a negative impact on bone quality at the tissue level. Here, we directly assess the structural and mechanical characteristics of cancellous bone from the lumbar vertebrae (L5) in non-treated osteoporotic controls (n=21), mid-term alendronate-treated osteoporotic patients (n=6), and long-term alendronate-treated osteoporotic patients (n=7). The strength and toughness of single trabeculae were evaluated, while the structure was characterised through measurements of microdamage accumulation, mineralisation distribution, and histological indices. The alendronate-treated cases had a reduced eroded surface (ES/BS, p<0.001) and a higher bone mineralisation in comparison to non-treated controls (p=0.037), which is indicative of low turnover associated with treatment. However, the amount of microdamage and the mechanical properties were similar among the control and treatment groups. As the tissue mineral density (TMD) increased significantly with alendronate treatment compared to non-treated osteoporotic controls, the reduction in resorption cavities could counterbalance the higher TMD allowing the alendronate-treated bone to maintain its mechanical properties and resist microdamage accumulation. A multivariate analysis of the possible predictors supports the theory that multiple factors (e.g., body mass index, TMD, and ES/BS) can impact the mechanical properties. Our results suggest that long-term alendronate treatment shows no adverse impact on mechanical cancellous bone characteristics.

KW - Aged

KW - Aged, 80 and over

KW - Alendronate

KW - Biomechanical Phenomena

KW - Bone Density Conservation Agents

KW - Bone Resorption

KW - Calcification, Physiologic

KW - Female

KW - Humans

KW - Lumbar Vertebrae

KW - Osteoporosis, Postmenopausal

M3 - SCORING: Journal article

C2 - 25241965

VL - 28

SP - 152

EP - 165

JO - EUR CELLS MATER

JF - EUR CELLS MATER

SN - 1473-2262

ER -