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Learning How glucosamine works


Advances in bone biology may lead to improved RA therapy


Promoting better surgical outcomes

Mortality increased in older women with RA


Scleroderma and kidney disease

Progress in lupus genetics

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Promoting better surgical outcomes

What is the problem and what is already known?
While joint replacement surgery remains one of the most effective treatments for severe arthritis affecting the hips and knees, artificial joints can wear down and shed small particles from the implant into the joint. These particles stimulate the release of cytokines that contribute to bone loss around the implant. The bone loss can cause loosening of the implant and require surgery to replace or revise the implant.  This surgery is painful, costly and often more complicated than the original surgery. As described in the previous article, a cytokine called RANKL has been identified as a key player in bone loss in osteoporosis, and most likely other forms of arthritis. Osteoprotegerin (OPG) has been found to block the action of RANKL but it is unknown whether use of OPG is effective in reducing bone loss following a joint implant.

Researchers funded by the Arthritis Foundation involved in the study: Paul Wooley, PhD & Shang-You Yang, MD, Wayne State University, Detroit.

Who was studied and what was done?
This study was done in mice to detect changes in bone following a technique that simulated a joint implant.

An innovative gene therapy approach was used to stimulate the production of OPG directly at the implant site.  

What were the study results?
Administration of the OPG gene therapy effectively reduced wear-related bone loss in experimental mice.

What’s the relevance to people with arthritis?
If effective in humans, this type of therapy may help delay or even prevent the need for revision surgery following a joint implant. Adds Dr. Wooley: “This approach to controlling bone loss may also be useful in the treatment of osteoporosis associated with rheumatoid arthritis. We are currently investigating whether OPG can be beneficial when combined with a biologic agent such as Enbrel.”

Source: Arthritis and Rheumatism, September 2002
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12355500&dopt=Abstract

 

Research Update is compiled by Michele Boutaugh, BSN, MPH, Medical and Scientific Affairs Department, National Office.

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