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Effect of ibandronate on bending strength and toughness of rodent cortical bone: Possible implications for fracture prevention

OBJECTIVES: There remains conflicting evidence regarding cortical bone strength following bisphosphonate therapy. As part of a study to assess the effects of bisphosphonate treatment on the healing of rat tibial fractures, the mechanical properties and radiological density of the uninjured contralat...

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Autores principales: Savaridas, T., Wallace, R. J., Dawson, S., Simpson, A. H. R. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: British Editorial Society of Bone and Joint Surgery 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4468982/
https://www.ncbi.nlm.nih.gov/pubmed/26062566
http://dx.doi.org/10.1302/2046-3758.46.2000311
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author Savaridas, T.
Wallace, R. J.
Dawson, S.
Simpson, A. H. R. W.
author_facet Savaridas, T.
Wallace, R. J.
Dawson, S.
Simpson, A. H. R. W.
author_sort Savaridas, T.
collection PubMed
description OBJECTIVES: There remains conflicting evidence regarding cortical bone strength following bisphosphonate therapy. As part of a study to assess the effects of bisphosphonate treatment on the healing of rat tibial fractures, the mechanical properties and radiological density of the uninjured contralateral tibia was assessed. METHODS: Skeletally mature aged rats were used. A total of 14 rats received 1µg/kg ibandronate (iban) daily and 17 rats received 1 ml 0.9% sodium chloride (control) daily. Stress at failure and toughness of the tibial diaphysis were calculated following four-point bending tests. RESULTS: Uninjured cortical bone in the iban group had a significantly greater mean (standard deviation (sd)), p < 0.001, stress at failure of 219.2 MPa (sd 45.99) compared with the control group (169.46 MPa (sd 43.32)) following only nine weeks of therapy. Despite this, the cortical bone toughness and work to failure was similar. There was no significant difference in radiological density or physical dimensions of the cortical bone. CONCLUSIONS: Iban therapy increases the stress at failure of uninjured cortical bone. This has relevance when normalising the strength of repair in a limb when comparing it with the unfractured limb. However, the 20% increase in stress at failure with iban therapy needs to be interpreted with caution as there was no corresponding increase in toughness or work to failure. Further research is required in this area, especially with the increasing clinical burden of low-energy diaphyseal femoral fractures following prolonged use of bisphosphonates. Cite this article: Bone Joint Res 2015;4:99–104
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spelling pubmed-44689822015-07-06 Effect of ibandronate on bending strength and toughness of rodent cortical bone: Possible implications for fracture prevention Savaridas, T. Wallace, R. J. Dawson, S. Simpson, A. H. R. W. Bone Joint Res General Orthopaedics OBJECTIVES: There remains conflicting evidence regarding cortical bone strength following bisphosphonate therapy. As part of a study to assess the effects of bisphosphonate treatment on the healing of rat tibial fractures, the mechanical properties and radiological density of the uninjured contralateral tibia was assessed. METHODS: Skeletally mature aged rats were used. A total of 14 rats received 1µg/kg ibandronate (iban) daily and 17 rats received 1 ml 0.9% sodium chloride (control) daily. Stress at failure and toughness of the tibial diaphysis were calculated following four-point bending tests. RESULTS: Uninjured cortical bone in the iban group had a significantly greater mean (standard deviation (sd)), p < 0.001, stress at failure of 219.2 MPa (sd 45.99) compared with the control group (169.46 MPa (sd 43.32)) following only nine weeks of therapy. Despite this, the cortical bone toughness and work to failure was similar. There was no significant difference in radiological density or physical dimensions of the cortical bone. CONCLUSIONS: Iban therapy increases the stress at failure of uninjured cortical bone. This has relevance when normalising the strength of repair in a limb when comparing it with the unfractured limb. However, the 20% increase in stress at failure with iban therapy needs to be interpreted with caution as there was no corresponding increase in toughness or work to failure. Further research is required in this area, especially with the increasing clinical burden of low-energy diaphyseal femoral fractures following prolonged use of bisphosphonates. Cite this article: Bone Joint Res 2015;4:99–104 British Editorial Society of Bone and Joint Surgery 2015-06-01 /pmc/articles/PMC4468982/ /pubmed/26062566 http://dx.doi.org/10.1302/2046-3758.46.2000311 Text en ©2015 The British Editorial Society of Bone & Joint Surgery © Wallace et al. This is an open-access article distributed under the terms of the Creative Commons Attributions licence, which permits unrestricted use, distribution, and reproduction in any medium, but not for commercial gain, provided the original author and source are credited.
spellingShingle General Orthopaedics
Savaridas, T.
Wallace, R. J.
Dawson, S.
Simpson, A. H. R. W.
Effect of ibandronate on bending strength and toughness of rodent cortical bone: Possible implications for fracture prevention
title Effect of ibandronate on bending strength and toughness of rodent cortical bone: Possible implications for fracture prevention
title_full Effect of ibandronate on bending strength and toughness of rodent cortical bone: Possible implications for fracture prevention
title_fullStr Effect of ibandronate on bending strength and toughness of rodent cortical bone: Possible implications for fracture prevention
title_full_unstemmed Effect of ibandronate on bending strength and toughness of rodent cortical bone: Possible implications for fracture prevention
title_short Effect of ibandronate on bending strength and toughness of rodent cortical bone: Possible implications for fracture prevention
title_sort effect of ibandronate on bending strength and toughness of rodent cortical bone: possible implications for fracture prevention
topic General Orthopaedics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4468982/
https://www.ncbi.nlm.nih.gov/pubmed/26062566
http://dx.doi.org/10.1302/2046-3758.46.2000311
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