This Wisconsin Alzheimer's Disease Research Center (ADRC) supports cutting-edge and innovative research on the etiology, pathogenesis, diagnosis and treatment of Alzheimer's disease (AD) and related illnesses by establishing a stimulating, interdisciplinary environment for collaborative research and by providing invaluable clinical and postmortem data and ante-mortem biospecimens. This proposal is to add advanced molecular imaging to the Center for tau and amyloid positron emission tomography (PET). The Wisconsin ADRC supports seven well-integrated Cores, including a Neuroimaging Core which will oversee the implementation, management and analysis of valuable new PET data from 300 ADRC participants. The Neuroimaging core is fully integrated with the other cores to support a full-spectrum of timely, innovative research including studies that will: 1) target antecedent biomarkers of preclinical stages of AD, 2) investigate the neurobiology of AD, 3) identify novel vascular and genetic risk factors and linking them to the disease pathology and clinical phenotype, 4) incorporate contemporary biochemical and molecular techniques into clinical-pathologic cohort studies, including genomics, epigenomics, proteomics and next generation genetic sequencing and 5) participate in national dementia research initiatives. The overall goals of the Wisconsin ADRC and its cores are enhanced by the proposed molecular imaging additions: The Administrative Core provides scientific leadership to the ADRC as a whole and will oversee sharing of data. The Clinical Core performs standardized UDS evaluations and will now have critical biomarker images to support its consensus diagnoses. The Outreach, Recruitment and Education (ORE) and the Minority Recruitment Satellite Program (MRSP) Cores will identify participants including underrepresented minorities to participate in this supplemental program. The Data Management and Statistical Core will assist in managing and analyzing the imaging data and derived values. The Neuropathology Core will advise on staging systems for the new images and conduct autopsy evaluations on subjects with ante-mortem molecular imaging. The ORE Core will provide a wide-range of educational and outreach programs regarding the importance of participation in brain donation and ante- mortem imaging, to recruit research volunteers, especially those of color into the proposed addition and Clinical Core. The MRSP Core will work closely with the ORE and Clinical Cores to enhance recruitment and retention of minority participants into the ADRC and into the proposed supplemental PET imaging. The Neuroimaging Core will conduct tau and amyloid PET imaging in addition to its existing cutting edge MRI protocols, will create centiloid maps for convenient interpretation, and will share the images. Findings from these studies will result in powerful investigations on early pathogenesis, identification and treatment for AD that will significantly reduce the human suffering and socio-economic devastations of the disease.

Public Health Relevance

This proposal seeks to augment the successful Wisconsin ADRC with new imaging techniques that will allow us to characterize the two major pathologies in Alzheimer's disease?the amyloid plaques and tau-related neurofibrillary tangles. It is now increasingly clear that these pathologies each develop several years prior to symptoms. A major focus of our center is on preclinical disease changes that occur in the brain. By studying the spatial burden of amyloid and tau we may be able to predict with greater certainty who goes on to develop symptomatic disease, understand protective and resilience factors in the presence of disease burden, and identify participants most appropriate for clinical trials.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Specialized Center (P50)
Project #
3P50AG033514-10S1
Application #
9209024
Study Section
Special Emphasis Panel (ZAG1)
Program Officer
Silverberg, Nina B
Project Start
2009-05-01
Project End
2019-03-31
Budget Start
2018-06-15
Budget End
2019-03-31
Support Year
10
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Brenowitz, Willa D; Han, Fang; Kukull, Walter A et al. (2018) Treated hypothyroidism is associated with cerebrovascular disease but not Alzheimer's disease pathology in older adults. Neurobiol Aging 62:64-71
Deming, Yuetiva; Dumitrescu, Logan; Barnes, Lisa L et al. (2018) Sex-specific genetic predictors of Alzheimer's disease biomarkers. Acta Neuropathol 136:857-872
Gleason, Carey E; Norton, Derek; Anderson, Eric D et al. (2018) Cognitive Variability Predicts Incident Alzheimer's Disease and Mild Cognitive Impairment Comparable to a Cerebrospinal Fluid Biomarker. J Alzheimers Dis 61:79-89
Tse, Kai-Hei; Cheng, Aifang; Ma, Fulin et al. (2018) DNA damage-associated oligodendrocyte degeneration precedes amyloid pathology and contributes to Alzheimer's disease and dementia. Alzheimers Dement 14:664-679
Schaffert, Jeff; LoBue, Christian; White, Charles L et al. (2018) Traumatic brain injury history is associated with an earlier age of dementia onset in autopsy-confirmed Alzheimer's disease. Neuropsychology 32:410-416
Dempsey, Robert J; Jackson, Daren C; Wilbrand, Stephanie M et al. (2018) The Preservation of Cognition 1 Year After Carotid Endarterectomy in Patients With Prior Cognitive Decline. Neurosurgery 82:322-328
Cummings, Nicole E; Williams, Elizabeth M; Kasza, Ildiko et al. (2018) Restoration of metabolic health by decreased consumption of branched-chain amino acids. J Physiol 596:623-645
Gallagher, Damien; Kiss, Alex; Lanctot, Krista L et al. (2018) Toward Prevention of Mild Cognitive Impairment in Older Adults With Depression: An Observational Study of Potentially Modifiable Risk Factors. J Clin Psychiatry 80:
Westmark, Cara J (2018) Fragile X and APP: a Decade in Review, a Vision for the Future. Mol Neurobiol :
Christensen, Krista; Gleason, Carey E; Mares, Julie A (2018) Dietary carotenoids and cognitive function among US adults, NHANES 2011-2014. Nutr Neurosci :1-9

Showing the most recent 10 out of 374 publications