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
Kirson, Noam Y; Scott Andrews, J; Desai, Urvi et al. (2018) Patient Characteristics and Outcomes Associated with Receiving an Earlier Versus Later Diagnosis of Probable Alzheimer's Disease. J Alzheimers Dis 61:295-307
Roe, Catherine M; Ances, Beau M; Head, Denise et al. (2018) Incident cognitive impairment: longitudinal changes in molecular, structural and cognitive biomarkers. Brain 141:3233-3248
La Joie, Renaud; Bejanin, Alexandre; Fagan, Anne M et al. (2018) Associations between [18F]AV1451 tau PET and CSF measures of tau pathology in a clinical sample. Neurology 90:e282-e290
Day, Gregory S; Musiek, Erik S; Morris, John C (2018) Rapidly Progressive Dementia in the Outpatient Clinic: More Than Prions. Alzheimer Dis Assoc Disord 32:291-297
Ihara, Ryoko; Vincent, Benjamin D; Baxter, Michael R et al. (2018) Relative neuron loss in hippocampal sclerosis of aging and Alzheimer's disease. Ann Neurol 84:741-753
Swarup, Vivek; Hinz, Flora I; Rexach, Jessica E et al. (2018) Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia. Nat Med :
Sato, Chihiro; Barthélemy, Nicolas R; Mawuenyega, Kwasi G et al. (2018) Tau Kinetics in Neurons and the Human Central Nervous System. Neuron 97:1284-1298.e7
Sutphen, Courtney L; McCue, Lena; Herries, Elizabeth M et al. (2018) Longitudinal decreases in multiple cerebrospinal fluid biomarkers of neuronal injury in symptomatic late onset Alzheimer's disease. Alzheimers Dement 14:869-879
Bussy, Aurélie; Snider, B Joy; Coble, Dean et al. (2018) Effect of apolipoprotein E4 on clinical, neuroimaging, and biomarker measures in noncarrier participants in the Dominantly Inherited Alzheimer Network. Neurobiol Aging 75:42-50
Vardarajan, Badri N; Barral, Sandra; Jaworski, James et al. (2018) Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease. Ann Clin Transl Neurol 5:406-417

Showing the most recent 10 out of 952 publications