The Neuropathology/Tissue Resource Core (NPTRC) provides essential neuropathology, quantitative morphometry/stereology, automated image analysis/lesion mapping and tissue banking support services to ADRC and outside investigators, projects, pilots and other Cores. NPTRC professional and technical staff is responsible for providing neuropathologic diagnoses based on NIA/AARP consensus age-adjusted quantitative criteria for Alzheimer's disease. Neuropathologic data are compared with Clinical and Psychometric Core data with the assistance of the Biostatistics Core. Brains for study will be obtained at autopsy from cognitively well characterized (WU Clinical Dementia Rating [CDR]), longitudinally studied subjects who are nondemented or who have probable DAT or related dementias. Other NPTRC services include participation in Consortium to Establish a Registry for Alzheimer's Disease (CERAD) activities, conducting weekly braincutting and microscopic diagnostic/teaching conferences dealing with AD and related dementias, providing quantitative morphometric data on AD marker lesions, including cerebral atrophy, senile plaques [SP], neurofibrillary pathology [neurofibrillary tangles (NFT), neuropil threads (NT), and neuritic senile plaques (N-SP)], and cerebral amyloid angiopathy (CAA) evaluation; neuronal stereologic analysis; and automated image analysis with large scale mapping and 3-D lesion spatial distribution (clustering) statistical analysis of SP and neurofibrillary pathology. AD-type lesions will be identified and quantified using a variety of conventional and specialized staining methods, including four silver methods, combined with immunohistochemical (IHC) marker-specific antibody probes. To complement these conventional diagnostic methods, we will also use a Core-developed sequential Gallyas silver and anti-betaA4 method to visualize the full range of SP and neurofibrillary lesions. At autopsy, fresh frozen and lightly fixed (suitable for IHC) brain tissue from defined sites and CSF samples will be obtained, stored at -85C and later distributed to ADRC and outside investigators. Antemortem blood and CSF samples will be similarly stored and distributed. These activities complement but are budgetarily and scientifically distinct from those of the Program Project, Healthy Aging and Senile Dementia (A003991).

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Specialized Center (P50)
Project #
3P50AG005681-16S2
Application #
6218682
Study Section
Project Start
1999-08-15
Project End
2000-04-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
16
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Washington University
Department
Type
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Joseph-Mathurin, Nelly; Su, Yi; Blazey, Tyler M et al. (2018) Utility of perfusion PET measures to assess neuronal injury in Alzheimer's disease. Alzheimers Dement (Amst) 10:669-677
Blue, Elizabeth E; Bis, Joshua C; Dorschner, Michael O et al. (2018) Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project. Dement Geriatr Cogn Disord 45:1-17
Kaur, Antarpreet; Edland, Steven D; Peavy, Guerry M (2018) The MoCA-Memory Index Score: An Efficient Alternative to Paragraph Recall for the Detection of Amnestic Mild Cognitive Impairment. Alzheimer Dis Assoc Disord 32:120-124
Hadjichrysanthou, Christoforos; McRae-McKee, Kevin; Evans, Stephanie et al. (2018) Potential Factors Associated with Cognitive Improvement of Individuals Diagnosed with Mild Cognitive Impairment or Dementia in Longitudinal Studies. J Alzheimers Dis 66:587-600
Rao, Shuquan; Ghani, Mahdi; Guo, Zhiyun et al. (2018) An APOE-independent cis-eSNP on chromosome 19q13.32 influences tau levels and late-onset Alzheimer's disease risk. Neurobiol Aging 66:178.e1-178.e8
Brenowitz, Willa D; Han, Fang; Kukull, Walter A et al. (2018) Treated hypothyroidism is associated with cerebrovascular disease but not Alzheimer's disease pathology in older adults. Neurobiol Aging 62:64-71
Hanfelt, John J; Peng, Limin; Goldstein, Felicia C et al. (2018) Latent classes of mild cognitive impairment are associated with clinical outcomes and neuropathology: Analysis of data from the National Alzheimer's Coordinating Center. Neurobiol Dis 117:62-71
Peloso, Gina M; van der Lee, Sven J; International Genomics of Alzheimer's Project (IGAP) et al. (2018) Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease. Alzheimers Dement (Amst) 10:595-598
Cruchaga, Carlos; Del-Aguila, Jorge L; Saef, Benjamin et al. (2018) Polygenic risk score of sporadic late-onset Alzheimer's disease reveals a shared architecture with the familial and early-onset forms. Alzheimers Dement 14:205-214
Kim, Sungsu; Maynard, Jason C; Strickland, Amy et al. (2018) Schwann cell O-GlcNAcylation promotes peripheral nerve remyelination via attenuation of the AP-1 transcription factor JUN. Proc Natl Acad Sci U S A 115:8019-8024

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