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Sunday, September 14, 2008

Various Advanced Approaches Help Better Therapies of Alzheimer's Disease


Various approaches in treating Alzheimer's disease could one-day lead to better therapies for the mind-robbing condition.


A trio of studies that were presented at the Alzheimer's Association 2008 International Conference on Alzheimer's Disease in Chicago pointed progress made on three different treatment fronts.

The first study involves a drug called Dimebon, which is an antihistamine, with positive results being reported from tests in Russia. Data from the Russian trials indicated that Dimebon might have value in treating Alzheimer's. In a controlled study, this buttressed American research reported earlier this year that showed improvements in Alzheimer's patients given Dimebon, which is believed to prevent the death of brain cells.

Researchers at the University of California, Los Angeles, have studied 183 people who had mild to moderate Alzheimer's disease. Mental function remained stable in those taking the drug, while it declined in those given a placebo. Mental function also stabilized in people who were first given a placebo after they began taking Dimebon.

The second trial used the body's immune system to prevent the mental deterioration suffered by people with Alzheimer's disease. The immune attack is aimed at the deposits of beta-amyloid protein that accumulate in the brains of patients. According to Nixon, the idea has been around for almost a decade now. The initial notion was to use the vaccine approach to prevent amyloid deposition, injecting amyloid so the body would attack the deposits. Now, the researchers are entering phase two, which is injecting the antibody itself.

Researchers at Eli Lilly & Co. have reported on 52 people with mild to moderate Alzheimer's. Some of them were given weekly injections of a monoclonal antibody that binds to beta amyloid, while others were injected with a placebo.

According to the researchers, detailed measurements have showed an increased level of beta amyloid in both blood and cerebrospinal fluid after 12 weeks in those getting the antibody, an indication that the beta amyloid in the brain might be starting to dissolve. New researches and studies of the therapy are planned.

Nixon viewed the results with "tempered optimism." He stated that one interesting finding was the response to the therapy was greatest in people who did not have a known genetic marker for Alzheimer's risk. "What is the significance of this? Why do carriers not respond?" Nixon asked. Moreover, he stated that the answer might help explain Alzheimer's disease better.

Meanwhile, a team at Weill Cornell Medical College in New York City reported a third study using a broad spectrum of antibodies. The treatment method was originally developed by Baxter International to treat autoimmune conditions. It was given to 24 people with mild to moderate Alzheimer's disease in a set of trials extending as long as 18 months. According to the researchers, statistically significant increases in mental function were seen in those getting the treatment. A large-scale, 18-month follow-up trial will be done.

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