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New Genes Linked to Alzheimer's

ByMICHAEL SMITHMedPage Today North American Correspondent
September 04, 2009, 7:09 PM

Sept. 6, 2009— -- Researchers have found new genes that are associated with an increased risk of Alzheimer's disease.

The three novel genes all appear to play a role in the deposits of a substance called amyloid in the brain -- deposits which characterize Alzheimer's. In this way, the genes resemble another gene which thus far is the only one that researchers have established increases the risk for the disease.

Experts hailed the findings as important new data that supports the role of amyloid in the disease, but most cautioned that there is no immediate significance in the clinical setting.

The three genes -- dubbed CLU, PICALM, and CR1 -- were reported in two separate studies, published online in the journal Nature Genetics, which used a method called genome-wide association scanning.

One study, led by Julie Williams of Cardiff University in the United Kingdom, identified CLU and PICALM as having a significant association with the disease.

The other study, led by Dr. Philippe Amouyel of the Institut Pasteur de Lille in Lille, France, also identified CLU, but instead of PICALM, his team found CR1.

While no treatments exist for Alzheimer's, Williams said, "If you took the effect of these genes (CLU and PICALM) out of the population, ideally you could reduce the number of people who develop Alzheimer's by 20 percent."

It is difficult to estimate risk, she added during a press conference, but "these effects are common and could potentially influence disease in a large number of people."

Although PICALM may play a role in the development of amyloid deposits, Williams said it may also affect how well neurons function.

In addition, the researcher said, CLU plays a role in inflammation, which many researchers believe to be a secondary effect of the disease.

"Our results suggest the possibility that inflammation may be a primary event in Alzheimer's disease," she said.

Exactly how the new genes function remains to be determined, said Dr. Michael Owen, a senior author of the British paper.

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