The proposed Alzheimer's Disease Center Core (ADCC) will provide research resources in the form of both clinical data and tissues for studies of Alzheimer's disease. Four cores, Administrative, Clinical, Neuropathology and Education and Information Transfer and four pilot studies are proposed. Core activities will be closely integrated, especially those of the Clinical and Neuropathology Cores. This will permit emphasis on four goals for the proposed ADCC: (1) Uniform, fully specified clinical and pathological evaluations for all participants, (2) Inclusion of both persons with Alzheimer's disease and fully comparable control individuals, (3) Obtaining longitudinal data from uniform, sequential annual clinical evaluations for both cases and controls, (4) Accurate clinical-pathological correlation from having clinical information proximate to death. The proposed ADCC will have the full support of the Rush Alzheimer's Disease Center (RADC) which has been in operation since 1985. The RADC receives partial funding from the State of Illinois and has been highly successful in providing services to Alzheimer's disease patients and their families. It is the single largest referral center for dementing illnesses in the Metropolitan Chicago area. The RADC offers three strong advantages to the proposed ADCC: (1) The ADCC will be assured of access to a large number of suitable patients. (2) Support from existing sources will enable some staff to contribute effort to the ADCC without charge. (3) There is a strong institutional commitment to Alzheimer's disease research that has been expressed both in recruitment of senior faculty and in provision of first-rate facilities.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
5P30AG010161-02
Application #
3101004
Study Section
Neuroscience, Behavior and Sociology of Aging Review Committee (NBSA)
Project Start
1991-09-30
Project End
1996-06-30
Budget Start
1992-07-15
Budget End
1993-06-30
Support Year
2
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Rush University Medical Center
Department
Type
DUNS #
City
Chicago
State
IL
Country
United States
Zip Code
60612
Kovaleva, Mariya A; Bilsborough, Elizabeth; Griffiths, Patricia C et al. (2018) Testing Tele-Savvy: Protocol for a randomized controlled trial. Res Nurs Health 41:107-120
Mahady, L; Nadeem, M; Malek-Ahmadi, M et al. (2018) HDAC2 dysregulation in the nucleus basalis of Meynert during the progression of Alzheimer's disease. Neuropathol Appl Neurobiol :
Lin, Ming; Gong, Pinghua; Yang, Tao et al. (2018) Big Data Analytical Approaches to the NACC Dataset: Aiding Preclinical Trial Enrichment. Alzheimer Dis Assoc Disord 32:18-27
Sekiya, Michiko; Wang, Minghui; Fujisaki, Naoki et al. (2018) Integrated biology approach reveals molecular and pathological interactions among Alzheimer's A?42, Tau, TREM2, and TYROBP in Drosophila models. Genome Med 10:26
Kommaddi, Reddy Peera; Das, Debajyoti; Karunakaran, Smitha et al. (2018) A? mediates F-actin disassembly in dendritic spines leading to cognitive deficits in Alzheimer's disease. J Neurosci 38:1085-1099
Mahady, Laura; Nadeem, Muhammad; Malek-Ahmadi, Michael et al. (2018) Frontal Cortex Epigenetic Dysregulation During the Progression of Alzheimer's Disease. J Alzheimers Dis 62:115-131
Hadjichrysanthou, Christoforos; McRae-McKee, Kevin; Evans, Stephanie et al. (2018) Potential Factors Associated with Cognitive Improvement of Individuals Diagnosed with Mild Cognitive Impairment or Dementia in Longitudinal Studies. J Alzheimers Dis 66:587-600
Crum, Jana; Wilson, Jeffrey; Sabbagh, Marwan (2018) Does taking statins affect the pathological burden in autopsy-confirmed Alzheimer's dementia? Alzheimers Res Ther 10:104
Wang, Dai; Schultz, Tim; Novak, Gerald P et al. (2018) Longitudinal Modeling of Functional Decline Associated with Pathologic Alzheimer's Disease in Older Persons without Cognitive Impairment. J Alzheimers Dis 62:855-865
Boyle, Patricia A; Yu, Lei; Wilson, Robert S et al. (2018) Person-specific contribution of neuropathologies to cognitive loss in old age. Ann Neurol 83:74-83

Showing the most recent 10 out of 786 publications