The string "13" can be converted to a number

Gilmour Osteopathy | News | Information | What's New
Prev   |  Next

Study on the value of glucosamine for hip and knee osteoarthritis

A new BMJ Study shows that Glucosamine with or without chondroitin is not helpful for osteoarthritis of the knee.
10 randomised controlled trials including studies of more than 200 patients , a total of over 3800 patients, were reviewed.
Compared with placebo, glucosamine, chondroitin, and their combination do not reduce joint pain or have an impact on narrowing of joint space.
There is no value for patients taking these supplements based on this evidence

 BMJ 2010; 341:c4675 doi: 10.1136/bmj.c4675 (Published 16 September 2010)

BMJ 2010; 341:c4675 doi: 10.1136/bmj.c4675 (Published 16 September 2010)
Cite this as: BMJ 2010; 341:c4675
Note - this paper is reproduced from the BMJ

Effects of glucosamine, chondroitin, or placebo in patients with osteoarthritis of hip or knee: network meta-analysis

Objective To determine the effect of glucosamine, chondroitin, or the two in combination on joint pain and on radiological progression of disease in osteoarthritis of the hip or knee.

Network meta-analysis. Direct comparisons within trials were combined with indirect evidence from other trials by using a Bayesian model that allowed the synthesis of multiple time points.
Main outcome measure Pain intensity. Secondary outcome was change in minimal width of joint space. The minimal clinically important difference between preparations and placebo was prespecified at −0.9 cm on a 10 cm visual analogue scale.

Data sources
Electronic databases and conference proceedings from inception to June 2009, expert contact, relevant websites.
Eligibility criteria for selecting studies Large scale randomised controlled trials in more than 200 patients with osteoarthritis of the knee or hip that compared glucosamine, chondroitin, or their combination with placebo or head to head.

10 trials in 3803 patients were included. On a 10 cm visual analogue scale the overall difference in pain intensity compared with placebo was −0.4 cm (95% credible interval −0.7 to −0.1 cm) for glucosamine, −0.3 cm (−0.7 to 0.0 cm) for chondroitin, and −0.5 cm (−0.9 to 0.0 cm) for the combination. For none of the estimates did the 95% credible intervals cross the boundary of the minimal clinically important difference. Industry independent trials showed smaller effects than commercially funded trials (P=0.02 for interaction). The differences in changes in minimal width of joint space were all minute, with 95% credible intervals overlapping zero.

 Compared with placebo, glucosamine, chondroitin, and their combination do not reduce joint pain or have an impact on narrowing of joint space. Health authorities and health insurers should not cover the costs of these preparations, and new prescriptions to patients who have not received treatment should be discouraged.

• We thank Bruno da Costa for helpful discussions related to minimal clinically important differences and limitations of effect sizes and Malcolm Sturdy for database development and maintenance.
• Contributors: SW and PJ contributed equally. PJ conceived the study. PJ, ST, and SW and were responsible for conception and design of the study. SW, PJ, NJW, and ST did the analysis and interpreted the analysis in collaboration with BT, EN, PMV, and SR. SW, PJ, BT, EN, SR, and ST were responsible for the acquisition of data. PJ and SW wrote the first draft of the manuscript. All authors critically revised the manuscript for important intellectual content and approved the final version of the manuscript. PJ and SR obtained public funding. PJ and PMV provided administrative, technical, and logistical support. PJ is guarantor.

• Funding: The study was funded by grants from the Swiss National Science Foundation’s National Research Program 53 on musculoskeletal health (PJ and SR) (No 4053-0-104762/3). PJ was a senior research fellow in the Program for Social Medicine, Preventive and Epidemiological Research funded by the Swiss National Science Foundation (grant No 3233-066377). SR was a recipient of a research fellowship funded by the Swiss National Science Foundation (grant No PBBEB-115067). SW was a recipient of an individual fellowship of the Janggen-Poehn-Foundation. The study sponsor had no role in study design, data collection, data synthesis, data interpretation, writing the report, or the decision to submit the manuscript for publication. None of the authors is affiliated with or funded by any manufacturer of any of the agents evaluated in this study.
Competing interests
 All authors have completed the Unified Competing Interest form at (available on request from the corresponding author) and declare: no support from any institution for the submitted work; no financial relationships with any institutions that might have an interest in the submitted work in the previous 3 years; no other relationships or activities that could appear to have influenced the submitted work. 
Ethical approval: Not required.

Send to friend          Ask a question 

Prev  |  Next