The overall goal of Religious Rush Orders Study Core is to provide detailed accurate longitudinal clinical, neuropsychological and neuropathologic data for persons without dementia, and for comparable persons with mild cognitive impairment and Alzheimer's disease to facilitate externally funded studies of aging and Alzheimer's disease, especially those requiring subject with no or mild cognitive impairment. There are three operational components to the proposed Core. 1) Detailed baseline clinical evaluation on men and women members of religious orders without overt dementia who are over the age of 65, understand the nature of the Core, and sign a brain donation form to document cognitive abilities at entry. 2) Detailed annual follow-up evaluation, identical to the baseline, to document change in cognitive function and clinical status proximate to death. 3) In conjunction with the Neuropathology Core, establish a mechanism to achieve high rates of brain autopsies, document the neuropathologic indices of Alzheimer's disease, and preserve the tissue in a fashion that retains maximum flexibility for use in a variety of experimental procedures. To accomplish these goals, the Core will build on its progress during the first funding period. From January 8, 1994 through August 15, 1995, uniform structured evaluations were performed on 176 Priests or Brothers, and 307 Nuns from Religious Orders in Chicago and five other cities across the country. Contacts have been made to enroll the additional 16? to meet the targeted panel size of 650. Of 315 eligible for their first year follow-up, 306 (97.1 %) have been evaluated. Twenty participants have died, 19 of whom underwent brain autopsy. Preliminary results based on cross-sectional analyses of a small number of persons occupying a narrow clinical spectrum from normality to mild cognitive impairment to very mild disease suggests that the proposed Core can provide a unique resource for definitive studies in this area.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
3P30AG010161-10S1
Application #
6340624
Study Section
Project Start
2000-08-15
Project End
2001-06-30
Budget Start
Budget End
Support Year
10
Fiscal Year
2000
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

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