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 #
2P50AG005146-12
Application #
2048987
Study Section
Special Emphasis Panel (ZAG1-CAG-7 (01))
Project Start
1984-09-28
Project End
1999-03-31
Budget Start
1994-08-10
Budget End
1995-03-31
Support Year
12
Fiscal Year
1994
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
Ting, Simon Kang Seng; Foo, Heidi; Chia, Pei Shi et al. (2018) Dyslexic Characteristics of Chinese-Speaking Semantic Variant of Primary Progressive Aphasia. J Neuropsychiatry Clin Neurosci 30:31-37
Eavani, Harini; Habes, Mohamad; Satterthwaite, Theodore D et al. (2018) Heterogeneity of structural and functional imaging patterns of advanced brain aging revealed via machine learning methods. Neurobiol Aging 71:41-50
Wang, Tingyan; Qiu, Robin G; Yu, Ming (2018) Predictive Modeling of the Progression of Alzheimer's Disease with Recurrent Neural Networks. Sci Rep 8:9161
Barnes, Josephine; Bartlett, Jonathan W; Wolk, David A et al. (2018) Disease Course Varies According to Age and Symptom Length in Alzheimer's Disease. J Alzheimers Dis 64:631-642
Agogo, George O; Ramsey, Christine M; Gnjidic, Danijela et al. (2018) Longitudinal associations between different dementia diagnoses and medication use jointly accounting for dropout. Int Psychogeriatr 30:1477-1487
Seddighi, Sahba; Varma, Vijay R; An, Yang et al. (2018) SPARCL1 Accelerates Symptom Onset in Alzheimer's Disease and Influences Brain Structure and Function During Aging. J Alzheimers Dis 61:401-414
Fredericks, Carolyn A; Sturm, Virginia E; Brown, Jesse A et al. (2018) Early affective changes and increased connectivity in preclinical Alzheimer's disease. Alzheimers Dement (Amst) 10:471-479
Holingue, Calliope; Wennberg, Alexandra; Berger, Slava et al. (2018) Disturbed sleep and diabetes: A potential nexus of dementia risk. Metabolism 84:85-93
Alosco, Michael L; Sugarman, Michael A; Besser, Lilah M et al. (2018) A Clinicopathological Investigation of White Matter Hyperintensities and Alzheimer's Disease Neuropathology. J Alzheimers Dis 63:1347-1360
van Bergen, Jiri M G; Li, Xu; Quevenco, Frances C et al. (2018) Low cortical iron and high entorhinal cortex volume promote cognitive functioning in the oldest-old. Neurobiol Aging 64:68-75

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