Down syndrome is a model for the study of Alzheimer's disease because almost 100% of middle-aged individuals with this condition show a specific pathogenic process that follows a predictable course of development. This study will develop and refine a paradigm for measuring signs of Alzheimer's disease in Down syndrome. The method proposed and developed here measures brain pathology and functional decline due to Alzheimer's disease. This research method combines a relatively new form of positron emission tomography, called [F-18]FDDNP PET (2-(1-{6- [(2-18F-fluoroethyl) (methyl) amino] -2-napthyl] ethylydene malononitrile, with (1) comparative neuropsychological test methods derived from animal studies of aging and cognition and (2) functional brain imaging (PET-FDG). The [F-18]FDDNP PET involves a radiolabeled probe that binds to A? plaques and neurofibrillary tangles and will be used to measure, in vivo, brain pathology in Down syndrome. Comparative neuropsychological tests with proven validity for people suffering from severe levels of cognitive impairment (e.g., mental retardation) will also be used. Rate of glucose metabolism based on PET-FDG has been effective in distinguishing individuals by stage of Alzheimer's disease, including individuals with Down syndrome. A cross-sectional design will include 40 adults with Down syndrome (20 demented and 20 unaffected), 20 individuals from the general community diagnosed with probable Alzheimer's disease, and 20 healthy controls. Results will extend preliminary studies and are expected to provide the means to more effectively track disease progress and assess treatment outcome. Consequently, this new method of detection stands not only to improve diagnosis and treatment for people with Down syndrome, but for the general population as well.

Public Health Relevance

Many people with Down syndrome suffer from Alzheimer's disease because of their genetic make-up. Early detection is important to help slow disease progression. This study is a first-ever attempt to assess the two major signs of Alzheimer's disease in the brains of living adults with Down syndrome. Results of this study stand to improve early detection of Alzheimer's disease in Down syndrome and in other individuals.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21AG030681-02
Application #
7845570
Study Section
Special Emphasis Panel (ZRG1-CND-E (90))
Program Officer
Hsiao, John
Project Start
2009-06-01
Project End
2012-05-31
Budget Start
2010-06-01
Budget End
2012-05-31
Support Year
2
Fiscal Year
2010
Total Cost
$157,850
Indirect Cost
Name
University of California Los Angeles
Department
Psychiatry
Type
Schools of Medicine
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095