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New Development In The Understanding Of Alzheimer’s Pathology

Alzheimer’s disease has been linked in many studies to buildup in the brain, but new research is finding a common thread between amyloid burden and lower energy levels, or metabolism, of neurons in certain areas of the brain associated with Alzheimer’s disease – even for people with no sign of cognitive decline. This is a new development in the understanding of Alzheimer’s pathology, say neuroscientists unveiling the research at the and Molecular Imaging’s 2013 Annual Meeting.

“This study shows that there is an association between and amyloid in the brains of normal people,” said Val J. Lowe, MD, a professor of radiology at Cancer Center based in Rochester, Minn. “Previous studies indicate that of this same pattern is present in patients who have abnormalities of the gene apolipoprotein E, or APOE. The hypothesis is that people who have these genetic abnormalities tend to have and are on the trajectory toward developing Alzheimer’s disease. does appear to be an early harbinger of the disease before dementia sets in.”

The research is a part of a longitudinal multi-phase study called the Mayo Clinic Study of Aging, which includes 2,500 patients with 4,000 projected for the next phase. For this imaging study, 617 cognitively normal subjects underwent two separate positron emission tomography (PET) procedures, a molecular imaging technique that visualizes physiological processes in the body. Each subject was imaged with an amyloid-binding radionuclide imaging agent, C-11 Pittsburgh compound B (PiB), produced on-site at the Mayo Clinic. An hour later, all patients were imaged again using the same scanner and a different radionuclide agent, F-18 fluorodeoxyglucose (FDG), which shows up on scans as hot-and-cold spots according to metabolic brain cell activity.

Results were then analyzed via quantitative analysis and reviewed. Researchers found significant hypometabolism in brain regions classically associated with Alzheimer’s disease, including the angular gyrus and posterior cingulate. Even the PiB PET scans that were deemed barely positive for amyloid were partnered with FDG PET scans that showed corresponding hypometabolism.

“In general, these findings were group-wide,” said Lowe. “We now need to parse the data down to an individual subject level to see what is driving this relationship. As we follow these subjects long term, this relationship will be important because if people have amyloid in their brain and survive without Alzheimer’s disease despite amyloid, we want to know why.”


Scientific Paper 467: Val Lowe, Kejal Kantarci, Clifford Jack, Radiology, Mayo Clinic, Rochester, MN; David Knopman, Bradley Boeve, Ronald Petersen, Neurology, Mayo Clinic, Rochester, MN; Stephen Weigand, Matthew Senjem, Biostatistics, Mayo Clinic, Rochester, MN, “FDG changes in PiB positive, cognitively normal subjects,” SNMMI’s 60th Annual Meeting, June 8 – 12, 2013, Vancouver, British Columbia.
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