After extensive development work, the Quantitative Morphometry Laboratory, Oregon Health Sciences University has reached the first level of functional performance of a newly assembled Image Analysis system capable of measuring neuritic plaque, neurofibrillary tangle, and amyloid burden within serially sectioned cerebral samples. Pilot studies recently completed have quantified plaque numbers form both hippocampal and neocortical samples of different brains, comparing manually obtained results by 3 independent observers, and matching these ranking orders with the data generated on the same samples through the Image Analysis system. This approach will be used to perfect a method for quantification of nerve cell numbers, completing all hardware and software modifications. This Image Analysis approach to quantitative neuropathological histomorphometry enables a more thorough sampling of large portions of gray matter during much shorter time, with the enhanced precision of computer-driven programs. The survey of hippocampal formation published earlier (Ball et al, 1988) automated observer analysis. this procedure required 3 months' technician's time per case. Most other quantitative sampling approaches actually analyze less than 0.1% of the total gyral gray matter. Our newly developed methodology will dramatically increase the rate of data acquisition, enabling surveys of up to 10% of actual, regional tissue volume in only a few days, with dramatically enhanced precision and reproducibility. In this fashion definitive correlations can be compared between neurological, psychological, and neuroimaging measurements and the true histopathological, severity of involvement in each lobe, from brains of both Alzheimer patients and age-matched normative controls.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG003991-14
Application #
6233968
Study Section
Project Start
1997-01-01
Project End
1997-12-31
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
14
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Washington University
Department
Type
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
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
Roe, Catherine M; Babulal, Ganesh M; Stout, Sarah H et al. (2018) Using the A/T/N Framework to Examine Driving in Preclinical AD. Geriatrics (Basel) 3:
Swarup, Vivek; Hinz, Flora I; Rexach, Jessica E et al. (2018) Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia. Nat Med :
Suárez-Calvet, Marc; Capell, Anja; Araque Caballero, Miguel Ángel et al. (2018) CSF progranulin increases in the course of Alzheimer's disease and is associated with sTREM2, neurodegeneration and cognitive decline. EMBO Mol Med 10:
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
Besser, Lilah; Kukull, Walter; Knopman, David S et al. (2018) Version 3 of the National Alzheimer's Coordinating Center's Uniform Data Set. Alzheimer Dis Assoc Disord 32:351-358
Su, Yi; Flores, Shaney; Hornbeck, Russ C et al. (2018) Utilizing the Centiloid scale in cross-sectional and longitudinal PiB PET studies. Neuroimage Clin 19:406-416
Kawamura, Naoki; Yokota, Tatsuya; Hontani, Hidekata (2018) Super-Resolution of Magnetic Resonance Images via Convex Optimization with Local and Global Prior Regularization and Spectrum Fitting. Int J Biomed Imaging 2018:9262847
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
Maxwell, Taylor J; Corcoran, Chris; Del-Aguila, Jorge L et al. (2018) Genome-wide association study for variants that modulate relationships between cerebrospinal fluid amyloid-beta 42, tau, and p-tau levels. Alzheimers Res Ther 10:86

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