Systemic alendronate prevents resorption of necrotic bone during revascularization. A bone chamber study in rats
(2002) In BMC Musculoskeletal Disorders 3.- Abstract
- Background: Avascular necrosis of bone (osteonecrosis) can cause structural failure and subsequent deformation, leading to joint dysfunction and pain. Structural failure is the result of resorption of necrotic bone during revascularization, before new bone has formed or consolidated enough for loadbearing. Bone resorption can be reduced by bisphosphonates. If resorption of the necrotic bone could be reduced during the revascularization phase until sufficient new bone has formed, it would appear that structural failure could be avoided. Methods: To test whether resorption of necrotic bone can be prevented, structural grafts were subjected to new bone ingrowth during systemic bisphosphonate treatment in a rat model. Results: In rats treated... (More)
- Background: Avascular necrosis of bone (osteonecrosis) can cause structural failure and subsequent deformation, leading to joint dysfunction and pain. Structural failure is the result of resorption of necrotic bone during revascularization, before new bone has formed or consolidated enough for loadbearing. Bone resorption can be reduced by bisphosphonates. If resorption of the necrotic bone could be reduced during the revascularization phase until sufficient new bone has formed, it would appear that structural failure could be avoided. Methods: To test whether resorption of necrotic bone can be prevented, structural grafts were subjected to new bone ingrowth during systemic bisphosphonate treatment in a rat model. Results: In rats treated with alendronate the necrotic bone was not resorbed, whereas it was almost entirely resorbed in the controls. Conclusion: Systemic alendronate treatment prevents resorption of necrotic bone during revascularization. In patients with osteonecrosis, bisphosphonates may therefore prevent collapse of the necrotic bone. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/317062
- author
- Åstrand, Jörgen LU and Aspenberg, Per LU
- organization
- publishing date
- 2002
- type
- Contribution to journal
- publication status
- published
- subject
- in
- BMC Musculoskeletal Disorders
- volume
- 3
- publisher
- BioMed Central (BMC)
- external identifiers
-
- pmid:12165099
- wos:000181476500019
- scopus:34248400391
- ISSN
- 1471-2474
- DOI
- 10.1186/1471-2474-3-19
- language
- English
- LU publication?
- yes
- id
- c50be297-6b08-4774-8217-e7d59de7b912 (old id 317062)
- date added to LUP
- 2016-04-01 17:15:32
- date last changed
- 2022-01-29 01:27:58
@article{c50be297-6b08-4774-8217-e7d59de7b912, abstract = {{Background: Avascular necrosis of bone (osteonecrosis) can cause structural failure and subsequent deformation, leading to joint dysfunction and pain. Structural failure is the result of resorption of necrotic bone during revascularization, before new bone has formed or consolidated enough for loadbearing. Bone resorption can be reduced by bisphosphonates. If resorption of the necrotic bone could be reduced during the revascularization phase until sufficient new bone has formed, it would appear that structural failure could be avoided. Methods: To test whether resorption of necrotic bone can be prevented, structural grafts were subjected to new bone ingrowth during systemic bisphosphonate treatment in a rat model. Results: In rats treated with alendronate the necrotic bone was not resorbed, whereas it was almost entirely resorbed in the controls. Conclusion: Systemic alendronate treatment prevents resorption of necrotic bone during revascularization. In patients with osteonecrosis, bisphosphonates may therefore prevent collapse of the necrotic bone.}}, author = {{Åstrand, Jörgen and Aspenberg, Per}}, issn = {{1471-2474}}, language = {{eng}}, publisher = {{BioMed Central (BMC)}}, series = {{BMC Musculoskeletal Disorders}}, title = {{Systemic alendronate prevents resorption of necrotic bone during revascularization. A bone chamber study in rats}}, url = {{http://dx.doi.org/10.1186/1471-2474-3-19}}, doi = {{10.1186/1471-2474-3-19}}, volume = {{3}}, year = {{2002}}, }