The continuing scientific progress in Alzheimer's disease (AD) relies on the availability of patients and controls for study, the reliability of the clinical diagnoses of dementia, and the interchange and collaboration between investigators across disciplines working on different aspects of the illness. The main goal of the Clinical Research Development Core is to facilitate the genetic family studies and the other multidisciplinary efforts of the Bryan ADRC by providing the basic patient material needed for these investigations. There are four specific aims of the Clinical Core: 1) Provide diagnostic assessment of patients with memory complaints. We plan to focus on continued high quality patient evaluation. We also will continue to explore ways to extend our services"""""""" to African American elderly who have been under-represented in the Center. 2) Identify from the patient base, probands and families appropriate for genetic family studies of Alzheimer's disease. There are over 50 families enrolled in the center in which there is multigenerational evidence of AD with autopsy confirmation. We plan to continue to develop additional informative families and to evaluate these participants either in the Memory Disorders Clinic or, for patients convenience, in the home. 3) Facilitate clinical research studies of Alzheimer's disease. The Clinical Core will continue to be a resource to the research studies of the Bryan ADRC and to external studies approved by the Research Resource and Review Committee. We also aim to explore ways to enhance clinical diagnosis (e.g. computerized assessment, diagnostic algorithms) thereby optimizing the quality of the data provided to collaborators. 4) Conduct therapeutic drug intervention trials for Alzheimer's disease. With the advances in the biology of AD, we expect that whole new classes of compounds may become available for testing in the near future. We have a well developed infrastructure for recruiting patients into studies. Through the Research and Resource Review Committee of Core B we plan to continue to screen for promising drug protocols for patients with memory disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Specialized Center (P50)
Project #
5P50AG005128-14
Application #
6234017
Study Section
Project Start
1997-05-01
Project End
1998-04-30
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
14
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Duke University
Department
Type
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
Petyuk, Vladislav A; Chang, Rui; Ramirez-Restrepo, Manuel et al. (2018) The human brainome: network analysis identifies HSPA2 as a novel Alzheimer’s disease target. Brain 141:2721-2739
Sims, Rebecca (see original citation for additional authors) (2017) Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nat Genet 49:1373-1384
Jun, Gyungah R; Chung, Jaeyoon; Mez, Jesse et al. (2017) Transethnic genome-wide scan identifies novel Alzheimer's disease loci. Alzheimers Dement 13:727-738
Hohman, Timothy J; Bush, William S; Jiang, Lan et al. (2016) Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium. Neurobiol Aging 38:141-150
Jun, G; Ibrahim-Verbaas, C A; Vronskaya, M et al. (2016) A novel Alzheimer disease locus located near the gene encoding tau protein. Mol Psychiatry 21:108-17
Hohman, Timothy J; Cooke-Bailey, Jessica N; Reitz, Christiane et al. (2016) Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk. Alzheimers Dement 12:233-43
Karch, Celeste M; Ezerskiy, Lubov A; Bertelsen, Sarah et al. (2016) Alzheimer's Disease Risk Polymorphisms Regulate Gene Expression in the ZCWPW1 and the CELF1 Loci. PLoS One 11:e0148717
Mez, Jesse; Mukherjee, Shubhabrata; Thornton, Timothy et al. (2016) The executive prominent/memory prominent spectrum in Alzheimer's disease is highly heritable. Neurobiol Aging 41:115-121
Ridge, Perry G; Hoyt, Kaitlyn B; Boehme, Kevin et al. (2016) Assessment of the genetic variance of late-onset Alzheimer's disease. Neurobiol Aging 41:200.e13-200.e20
Ghani, Mahdi; Reitz, Christiane; Cheng, Rong et al. (2015) Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals. JAMA Neurol 72:1313-23

Showing the most recent 10 out of 97 publications