This application proposes continuation of the Rush Alzheimer's Disease Core Center (ADCC) that was originally funded in July, 1991. The Center initially had four cores: Administrative, Clinical, Neuropathology and Education and Information Transfer. Two additional cores were subsequently added through competitive supplements: the Religious Orders Study Core in July, 1993 and the Epidemiology and Biostatistics Core in July, 1995. The central goal of the ADCC continues to be providing core resources for Alzheimer's disease research of high scientific quality. Because the ADCC itself is not intended to conduct hypothesis driven research directly, there is strong emphasis on development of externally funded studies, especially efforts that are of sufficient merit to achieve NIH funding. Selection of the best pilot projects is essential to achieving this goal. Pilot applications are accepted not only from Rush faculty but from all Chicago-area Alzheimer's disease investigators and are evaluated through a structured, competitive process that emphasizes identification of pilot projects with the greatest potential for leading to new full-scale studies. Three unusual circumstances shape the Rush ADCC and the approach to its overall goal: (a) There is strong emphasis on large-scale longitudinal data collection and analysis that arises from an understanding of the importance of these approaches to answering crucial questions about Alzheimer's disease and from the presence at Rush of investigators familiar with the necessary techniques. (b)The presence at Rush of a State-of-Illinois-funded program that provides services for Alzheimer's disease patients and their families and that conducts extensive educational efforts has permitted the ADCC to develop an unusually large patient base and to focus on information transfer efforts for minority groups. (c) The opportunity, through the Religious Orders Study Core, for obtaining tissue from persons who have been carefully characterized clinically by sequential annual evaluations provides especially strong opportunities for precise clinical pathological correlations and for investigating the spectrum between Alzheimer's disease and normal cognition.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
5P30AG010161-08
Application #
2732525
Study Section
Special Emphasis Panel (ZAG1-DAG-4 (30))
Project Start
1991-09-30
Project End
2001-06-30
Budget Start
1998-07-01
Budget End
1999-06-30
Support Year
8
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Rush University Medical Center
Department
Type
DUNS #
City
Chicago
State
IL
Country
United States
Zip Code
60612
Tasaki, Shinya; Gaiteri, Chris; Mostafavi, Sara et al. (2018) The Molecular and Neuropathological Consequences of Genetic Risk for Alzheimer's Dementia. Front Neurosci 12:699
Burke, Shanna L; Cadet, Tamara; Maddux, Marlaina (2018) Chronic Health Illnesses as Predictors of Mild Cognitive Impairment Among African American Older Adults. J Natl Med Assoc 110:314-325
Hanfelt, John J; Peng, Limin; Goldstein, Felicia C et al. (2018) Latent classes of mild cognitive impairment are associated with clinical outcomes and neuropathology: Analysis of data from the National Alzheimer's Coordinating Center. Neurobiol Dis 117:62-71
Oveisgharan, Shahram; Arvanitakis, Zoe; Yu, Lei et al. (2018) Sex differences in Alzheimer's disease and common neuropathologies of aging. Acta Neuropathol 136:887-900
Guo, Caiwei; Jeong, Hyun-Hwan; Hsieh, Yi-Chen et al. (2018) Tau Activates Transposable Elements in Alzheimer's Disease. Cell Rep 23:2874-2880
Felsky, Daniel; Patrick, Ellis; Schneider, Julie A et al. (2018) Polygenic analysis of inflammatory disease variants and effects on microglia in the aging brain. Mol Neurodegener 13:38
Malek-Ahmadi, Michael; Chen, Kewei; Perez, Sylvia E et al. (2018) Cognitive composite score association with Alzheimer's disease plaque and tangle pathology. Alzheimers Res Ther 10:90
Kamara, Dennis M; Gangishetti, Umesh; Gearing, Marla et al. (2018) Cerebral Amyloid Angiopathy: Similarity in African-Americans and Caucasians with Alzheimer's Disease. J Alzheimers Dis 62:1815-1826
Zhou, Zilu; Wang, Weixin; Wang, Li-San et al. (2018) Integrative DNA copy number detection and genotyping from sequencing and array-based platforms. Bioinformatics 34:2349-2355
Cheng, Hao; Xuan, Hongwen; Green, Christopher D et al. (2018) Repression of human and mouse brain inflammaging transcriptome by broad gene-body histone hyperacetylation. Proc Natl Acad Sci U S A 115:7611-7616

Showing the most recent 10 out of 786 publications