The Neuropathology Core (Core C), a central component of our Alzheimer's Disease Research Center (ADRC), arranges and conducts autopsies, performs neuropathological evaluations of human subjects (Core B, Project), and assists in the assessment of transgenic (Tg) animal models of Ad (Projects 1-3). To support research that requires brains from humans, Core C operates the Brain Resource Center (BRC), a repository of fixed/frozen autopsy tissues. The faculty of Core C plays a critical role in training basic scientists and physicians in the pathology of aging and neurodegenerative diseases, consults with outside pathologists on cases of dementia, and does genotyping relevant to AD. The Core C prospective autopsy program is unique because of the large proportion of control subjects from the Baltimore Longitudinal Study of Aging (BLSA) (Core B). During the next five years, we project a total of 113 autopsies, 71 of which will be longitudinally characterized subjects from the BLSA. Many of these individuals will have had neuroimaging studies as part of a parallel NIA study. Tissues from these subjects as well as from other cases of AD will be accessed to the BRC and will continue to be made available for research, not only within the ADRC, but to the scientific community at large. Core C will support morphological studies of Tg mice that recapitulate several of the APPswe Tg mice recapitulate several of the pathological features of AD (Projects 1-3). Many of these analyses will require quantitative morphometry and, thereby, support will require the assistance of the histology laboratory and stereology unit. Through these multiple activities, Core C acts to facilitate and coordinate the evaluations of both clinical and experimental in Projects 1-4, thereby greatly enhancing the diagnostic and research capabilities of our ADRC.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Specialized Center (P50)
Project #
2P50AG005146-17
Application #
6210907
Study Section
Special Emphasis Panel (ZAG1-PCR-3 (J5))
Project Start
1984-09-28
Project End
2004-03-31
Budget Start
Budget End
Support Year
17
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
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
Brent, Robert J (2018) Estimating the monetary benefits of medicare eligibility for reducing the symptoms of dementia. Appl Econ 50:6327-6340
Kim, Sangjune; Yun, Seung Pil; Lee, Saebom et al. (2018) GBA1 deficiency negatively affects physiological ?-synuclein tetramers and related multimers. Proc Natl Acad Sci U S A 115:798-803
Deming, Yuetiva; Dumitrescu, Logan; Barnes, Lisa L et al. (2018) Sex-specific genetic predictors of Alzheimer's disease biomarkers. Acta Neuropathol 136:857-872
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
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
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

Showing the most recent 10 out of 830 publications