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Arthritis Drug May Have Role In Treating Alzheimer's

By John Schieszer, Medical Tribune News Service.

VANCOUVER, CANADA -- Canadian researchers say a new class of drugs recently approved to treat the pain and inflammation of arthritis, called COX-2 inhibitors, may have a role in preventing and treating Alzheimer's disease (AD).

``What you are after in dealing with Alzheimer's disease is to reduce the inflammation in the brain,'' said Dr. Patrick McGeer of Kinsmen Laboratory of Neurological Research at the University of British Columbia. ``One hopes these will work because treatments for Alzheimer's disease are desperately needed and there is very strong data that the nonsteroidal anti-inflammatory drugs (drugs such as ibuprofen used to treat arthritis) will work in this disease. It is just people are afraid of the gastrointestinal side effects.''

Two COX-2 inhibitors have recently been approved by the Food and Drug Administration. These drugs, celecoxib (Celebrex) and rofecoxib (Vioxx) now both are being tested in clinical trials with AD patients.

Speaking at the Ninth International Congress of the International Psychogeriatric Association (IPA) in here on Aug. 17, McGeer presented data on what role COX-2 inhibitors may have in the treatment of AD.

``To date there is no approved treatment that will delay the death of neurons so at the present time people with Alzheimer's disease are condemned to a loss of neurons as though there were no treatment at all,'' said McGeer. ``The NSAIDs offer promise of delaying or perhaps even preventing neuronal death. That is why it is so urgent that this type of treatment be evaluated.''

COX-2 inhibitors work by inhibiting the enzyme COX-2 without significantly inhibiting COX-1. COX-1 produces prostaglandins that are believed to be responsible for maintaining normal body functions, including the protection of the lining of the stomach. COX-2 is responsible for producing prostaglandins that are believed to be primarily responsible for pain and inflammation. NSAIDs inhibit both COX-1 and COX-2, which can result in more stomach upset.

``COX-2 inhibitors appear promising because they may slow down some of the inflammatory response that mediates the damage in Alzheimer's disease,'' said Preston Mason, who is an associate professor of biochemistry and medicine at MCP Hahnemann School of Medicine in Pittsburgh.

But despite these theories of how COX-2 inhibitors may help in AD, some AD researchers say they may be less effective than NSAIDs. While COX-2 inhibitors result in fewer serious gastrointestinal side effects than traditional NSAIDs, making them good candidates for long-term therapy, they also may be too specific in their action.

``The short answer is we just don't know,'' said Dr. John Morris, who is a professor of neurology at Washington University School of Medicine in St. Louis. ``The first study may report results in the next six to 12 months. Frankly, I don't think we will have the full story.'' He added: ``The COX-2 inhibitors are very attractive because of their side effect profile, but we don't [yet] know the COX-2 enzyme distribution in the brain.''


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