Cargando…

Bisphosphonates therapy for osteoarthritis: a meta-analysis of randomized controlled trials

High-turnover type bone metabolism derangement has been considered to be one of the major causes of osteoarthritis (OA). Bisphosphonates can attach to hydroxyapatite binding sites on bony surfaces, particularly those which are undergoing active bone resorption. To evaluate the effectiveness of bisph...

Descripción completa

Detalles Bibliográficos
Autores principales: Xing, R. L., Zhao, L. R., Wang, P. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5047862/
https://www.ncbi.nlm.nih.gov/pubmed/27757376
http://dx.doi.org/10.1186/s40064-016-3359-y
_version_ 1782457485086425088
author Xing, R. L.
Zhao, L. R.
Wang, P. M.
author_facet Xing, R. L.
Zhao, L. R.
Wang, P. M.
author_sort Xing, R. L.
collection PubMed
description High-turnover type bone metabolism derangement has been considered to be one of the major causes of osteoarthritis (OA). Bisphosphonates can attach to hydroxyapatite binding sites on bony surfaces, particularly those which are undergoing active bone resorption. To evaluate the effectiveness of bisphosphonates in OA treatment, literature databases were searched from inception to February 28, 2016 for clinical studies of bisphosphonates for OA treatment. All randomized controlled trials in which bisphosphonates therapy was compared with a placebo or a conventional medication, were selected. 15/1145 studies were eligible for analysis, which included 3566 participants. Bisphosphonates therapy improved pain, stiffness and function significantly in OA assessed by the Western Ontario and McMaster Universities Arthritis Index scale (MD = 4.59; 95 % CI 2.83–6.34; P < 0.00001; MD = 1.43; 95 % CI 0.83–2.23; P = 0.0005; MD = 2.01; 95 % CI 1.27–2.75; P < 0.00001). Bisphosphonates also reduced osteophyte score significantly (MD = −0.51; 95 % CI −0.84 to −0.19; P = 0.002). However, no significant differences were found in subjective improvement, osteoarthritis progression, the number of required acetaminophen treatment or joint replacement. In conclusion, bisphosphonates therapy is effective in relieving pain,stiffness and accelerating functional recovery in OA. Limitations of the studies we analysed included the differences in duration of bisphosphonates use, the doses and types of bisphosphonates and the lack of long-term data on OA joint structure modification after bisphosphonates therapy. More targeted studies are required to evaluate on the effectiveness of bisphosphonates for OA treatment.
format Online
Article
Text
id pubmed-5047862
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Springer International Publishing
record_format MEDLINE/PubMed
spelling pubmed-50478622016-10-18 Bisphosphonates therapy for osteoarthritis: a meta-analysis of randomized controlled trials Xing, R. L. Zhao, L. R. Wang, P. M. Springerplus Review High-turnover type bone metabolism derangement has been considered to be one of the major causes of osteoarthritis (OA). Bisphosphonates can attach to hydroxyapatite binding sites on bony surfaces, particularly those which are undergoing active bone resorption. To evaluate the effectiveness of bisphosphonates in OA treatment, literature databases were searched from inception to February 28, 2016 for clinical studies of bisphosphonates for OA treatment. All randomized controlled trials in which bisphosphonates therapy was compared with a placebo or a conventional medication, were selected. 15/1145 studies were eligible for analysis, which included 3566 participants. Bisphosphonates therapy improved pain, stiffness and function significantly in OA assessed by the Western Ontario and McMaster Universities Arthritis Index scale (MD = 4.59; 95 % CI 2.83–6.34; P < 0.00001; MD = 1.43; 95 % CI 0.83–2.23; P = 0.0005; MD = 2.01; 95 % CI 1.27–2.75; P < 0.00001). Bisphosphonates also reduced osteophyte score significantly (MD = −0.51; 95 % CI −0.84 to −0.19; P = 0.002). However, no significant differences were found in subjective improvement, osteoarthritis progression, the number of required acetaminophen treatment or joint replacement. In conclusion, bisphosphonates therapy is effective in relieving pain,stiffness and accelerating functional recovery in OA. Limitations of the studies we analysed included the differences in duration of bisphosphonates use, the doses and types of bisphosphonates and the lack of long-term data on OA joint structure modification after bisphosphonates therapy. More targeted studies are required to evaluate on the effectiveness of bisphosphonates for OA treatment. Springer International Publishing 2016-10-03 /pmc/articles/PMC5047862/ /pubmed/27757376 http://dx.doi.org/10.1186/s40064-016-3359-y Text en © The Author(s) 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.
spellingShingle Review
Xing, R. L.
Zhao, L. R.
Wang, P. M.
Bisphosphonates therapy for osteoarthritis: a meta-analysis of randomized controlled trials
title Bisphosphonates therapy for osteoarthritis: a meta-analysis of randomized controlled trials
title_full Bisphosphonates therapy for osteoarthritis: a meta-analysis of randomized controlled trials
title_fullStr Bisphosphonates therapy for osteoarthritis: a meta-analysis of randomized controlled trials
title_full_unstemmed Bisphosphonates therapy for osteoarthritis: a meta-analysis of randomized controlled trials
title_short Bisphosphonates therapy for osteoarthritis: a meta-analysis of randomized controlled trials
title_sort bisphosphonates therapy for osteoarthritis: a meta-analysis of randomized controlled trials
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5047862/
https://www.ncbi.nlm.nih.gov/pubmed/27757376
http://dx.doi.org/10.1186/s40064-016-3359-y
work_keys_str_mv AT xingrl bisphosphonatestherapyforosteoarthritisametaanalysisofrandomizedcontrolledtrials
AT zhaolr bisphosphonatestherapyforosteoarthritisametaanalysisofrandomizedcontrolledtrials
AT wangpm bisphosphonatestherapyforosteoarthritisametaanalysisofrandomizedcontrolledtrials