Our Alzheimer's Disease Research Center (ADRC) has a major commitment to investigations of aging and age-associated diseases, including illnesses that occur in subjects with Alzheimer's disease (AD) and in older individuals with Down's Syndrome (DS). We believe that genetic factors, abnormalities of protein processing, and age play important roles in the cognitive/memory impairments and in the brain pathology that occur in these individuals. The interface between biological processes and clinical issues (i.e., subtypes of disease, risk and prognostic factors, and relationship of clinical phenotype to brain pathology) are addressed in Cores B and C. At a basic science level, we need more information about the mechanisms that lead to: selective vulnerability of specific neurons; cytoskeletal abnormalities in these cells; the formation of senile plaques; the pathways by which disease spreads; and the occurrence of death of neurons. Moreover, no therapies are available for these disorders. Building upon Core support, Projects 1-6 address some of these issues, focusing on clinical-pathological correlations (Project 2,3,5), the problems of selective vulnerability and the spatial/temporal evolution of pathology (Projects 1,3,4), and molecular mechanisms that lead to neuronal abnormalities characteristic of aging (Projects 1,2), AD (Projects 1,4,5), and DS (Projects 1,3). We believe that these disorders may eventually be amenable to therapeutic approaches, and, in Project 6, we test three biological therapies (i.e., nerve growth factor, peripheral nerve grafts, and neural grafts) designed to influence basal forebrain cholinergic neurons in several animal models. Ultimately, these lines of research should provide new insights into the natural history of the disease, predictors of prognosis, mechanisms of cellular pathology, and, possibly, new approaches to treatment. Finally, our ADRC is committed to the training of young physicians/scientists who represent our best hope for eventually being able to deal with age-associated disorders, such as AD.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Specialized Center (P50)
Project #
5P50AG005146-11
Application #
3104835
Study Section
Aging Review Committee (AGE)
Project Start
1984-09-28
Project End
1994-03-31
Budget Start
1993-07-05
Budget End
1994-03-31
Support Year
11
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Hohman, Timothy J; Dumitrescu, Logan; Barnes, Lisa L et al. (2018) Sex-Specific Association of Apolipoprotein E With Cerebrospinal Fluid Levels of Tau. JAMA Neurol 75:989-998
Burke, Shanna L; Maramaldi, Peter; Cadet, Tamara et al. (2018) Decreasing hazards of Alzheimer's disease with the use of antidepressants: mitigating the risk of depression and apolipoprotein E. Int J Geriatr Psychiatry 33:200-211
Kales, Helen C; Gitlin, Laura N; Stanislawski, Barbara et al. (2018) Effect of the WeCareAdvisor™ on family caregiver outcomes in dementia: a pilot randomized controlled trial. BMC Geriatr 18:113
Kageyama, Yusuke; Saito, Atsushi; Pletnikova, Olga et al. (2018) Amyloid ? toxic conformer has dynamic localization in the human inferior parietal cortex in absence of amyloid plaques. Sci Rep 8:16895
Reagh, Zachariah M; Noche, Jessica A; Tustison, Nicholas J et al. (2018) Functional Imbalance of Anterolateral Entorhinal Cortex and Hippocampal Dentate/CA3 Underlies Age-Related Object Pattern Separation Deficits. Neuron 97:1187-1198.e4
Qian, Winnie; Fischer, Corinne E; Schweizer, Tom A et al. (2018) Association Between Psychosis Phenotype and APOE Genotype on the Clinical Profiles of Alzheimer's Disease. Curr Alzheimer Res 15:187-194
Samus, Quincy M; Black, Betty Smith; Bovenkamp, Diane et al. (2018) Home is where the future is: The BrightFocus Foundation consensus panel on dementia care. Alzheimers Dement 14:104-114
Gallagher, Damien; Kiss, Alex; Lanctot, Krista et al. (2018) Depression and Risk of Alzheimer Dementia: A Longitudinal Analysis to Determine Predictors of Increased Risk among Older Adults with Depression. Am J Geriatr Psychiatry 26:819-827
Tse, Kai-Hei; Cheng, Aifang; Ma, Fulin et al. (2018) DNA damage-associated oligodendrocyte degeneration precedes amyloid pathology and contributes to Alzheimer's disease and dementia. Alzheimers Dement 14:664-679
Shi, Liu; Baird, Alison L; Westwood, Sarah et al. (2018) A Decade of Blood Biomarkers for Alzheimer's Disease Research: An Evolving Field, Improving Study Designs, and the Challenge of Replication. J Alzheimers Dis 62:1181-1198

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