The Alzheimer's Disease Research Center (ADRC) at the Johns Hopkins Medical Institutions (JHMI) has a commitment to investigations of aging and age-associated diseases, particularly Alzheimer's disease (AD). Because of the importance of age and genetic factors in the etiologies of AD, the principal research focus of our ADRC is on the roles of age and genes in these processes. Thus, with the support of Cores, the research in Kawas' Project focuses on behavior-brain correlations in intact aged individuals, elderly subjects with mild cognitive impairments, and cases of AD at various stages of the disease. Of particular importance are the studies of the Baltimore Longitudinal Study of Aging (BLSA) cohort, a unique, extraordinarily well-characterized group of subjects that have been followed for up to 30 years. Some of these individuals will have serial imaging studies. Moreover, these elderly subjects, who have detailed neuropsychological examinations, have consented to autopsy so that brain tissues will be available for research. Supported by the Neuropathology Core, Projects 18-20 take advantage of transgenic technologies: to produce mice with mutations in the amyloid precursor protein (APP) gene linked to familial AD or hereditary cerebral hemorrhage with amyloid, Dutch type; to introduce SOD1 genes with mutations linked to familial amyotrophic lateral sclerosis into the mouse germline; and to overexpress or ablate the APP gene. These animals will be studied using a variety of neurobiological strategies that have proved to be very successful in other animal models of age-associated disorders. These models will be of great value in testing the etiological roles of these mutations in disease, in examining the character/evolution of the pathology, in determining mechanisms of cell dysfunction/death, and eventually, in testing novel therapies. Additional studies relevant to aging and neurodegenerative diseases are supported by our Pilots. Finally, our ADRC is committed to training young physicians and scientists and in disseminating information concerning age-associated diseases to families, caregivers, and other health professionals.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Specialized Center (P50)
Project #
5P50AG005146-13
Application #
2048988
Study Section
Special Emphasis Panel (ZAG1-CAG-7 (01))
Project Start
1984-09-28
Project End
1999-03-31
Budget Start
1995-08-15
Budget End
1996-03-31
Support Year
13
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Pathology
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
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
Ganguli, Mary; Albanese, Emiliano; Seshadri, Sudha et al. (2018) Population Neuroscience: Dementia Epidemiology Serving Precision Medicine and Population Health. Alzheimer Dis Assoc Disord 32:1-9
Tsapkini, Kyrana; Webster, Kimberly T; Ficek, Bronte N et al. (2018) Electrical brain stimulation in different variants of primary progressive aphasia: A randomized clinical trial. Alzheimers Dement (N Y) 4:461-472
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
Ramsey, Christine M; Gnjidic, Danijela; Agogo, George O et al. (2018) Longitudinal patterns of potentially inappropriate medication use following incident dementia diagnosis. Alzheimers Dement (N Y) 4:1-10
Riello, Marianna; Faria, Andreia V; Ficek, Bronte et al. (2018) The Role of Language Severity and Education in Explaining Performance on Object and Action Naming in Primary Progressive Aphasia. Front Aging Neurosci 10:346
Chen, Lin; Wei, Zhiliang; Chan, Kannie W Y et al. (2018) Protein aggregation linked to Alzheimer's disease revealed by saturation transfer MRI. Neuroimage 188:380-390
Ayhan, Fatma; Perez, Barbara A; Shorrock, Hannah K et al. (2018) SCA8 RAN polySer protein preferentially accumulates in white matter regions and is regulated by eIF3F. EMBO J 37:
Sathe, Gajanan; Na, Chan Hyun; Renuse, Santosh et al. (2018) Phosphotyrosine profiling of human cerebrospinal fluid. Clin Proteomics 15:29
Martin, Lee J; Chang, Qing (2018) DNA Damage Response and Repair, DNA Methylation, and Cell Death in Human Neurons and Experimental Animal Neurons Are Different. J Neuropathol Exp Neurol 77:636-655

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