The neuropathology core is maintained by a professional staff of Lawrence Hansen, M.D. and Eliezer Masliah, M.D. Its functions include neuropathologic and neurochemical analyses of autopsy specimens from patients clinical evaluated at the ADRC, and maintenance of a brain tissue bank of frozen and fixed material from such clinically and neuropathologically characterized patients. On the basis of the past several years experience, we anticipate receiving 50-60 brains annually, mostly originating from the ADRC. In may cases, rapid autopsies (within 8 hours of death) allow fresh brain tissues to be distributed to ADRC affiliated research laboratories for use in RNA biochemistry, in situ hybridization/autoradiography, and immunohistochemistry. After removing the appropriate fresh tissue blocks for such studies, the right hemibrain is frozen at 70. This specimen is utilized for neurochemical measurements of choline acetyltransferase, somatostatin, and synaptophysin, as well as for western blot analyses to determine antibody sensitivities and specificities for correlations with various immunohistochemical studies. Frozen brain tissue is also available for distribution to other ADRC investigators. Neuropathologic studies are carried out on the formalin fixed left hemibrain, and involve multiple stains on multiple blocks from all parts of the brain. Diagnoses are established by the location and concentration of plaques and tangles as quantified with thioflavin and Bielschowsky preparations. We will also neuropathologically stage the extent of Alzheimer disease pathology in Alzheimer cases and in our elderly controls using the staging classification of Braak and Braak. Other diagnoses are added or ruled- out. Lewy body disease is evaluated with both H&E and anti-ubiquitin immunohistochemical preparations. Cresyl violet stained section are used for neocortical cell counting by image analysis. All data are recorded in the computerized data base of this core, as well as in the ADRC main computer.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Specialized Center (P50)
Project #
5P50AG005131-13
Application #
5204440
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
13
Fiscal Year
1996
Total Cost
Indirect Cost
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
Chen, Xu-Qiao; Fang, Fang; Florio, Jazmin B et al. (2018) T-complex protein 1-ring complex enhances retrograde axonal transport by modulating tau phosphorylation. Traffic 19:840-853
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
Zhou, Zilu; Wang, Weixin; Wang, Li-San et al. (2018) Integrative DNA copy number detection and genotyping from sequencing and array-based platforms. Bioinformatics 34:2349-2355
Burke, Shanna L; Hu, Tianyan; Fava, Nicole M et al. (2018) Sex differences in the development of mild cognitive impairment and probable Alzheimer's disease as predicted by hippocampal volume or white matter hyperintensities. J Women Aging :1-25
Wang, Qi; Guo, Lei; Thompson, Paul M et al. (2018) The Added Value of Diffusion-Weighted MRI-Derived Structural Connectome in Evaluating Mild Cognitive Impairment: A Multi-Cohort Validation1. J Alzheimers Dis 64:149-169
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
Sundermann, Erin E; Tran, My; Maki, Pauline M et al. (2018) Sex differences in the association between apolipoprotein E ?4 allele and Alzheimer's disease markers. Alzheimers Dement (Amst) 10:438-447
Edmonds, Emily C; Weigand, Alexandra J; Thomas, Kelsey R et al. (2018) Increasing Inaccuracy of Self-Reported Subjective Cognitive Complaints Over 24 Months in Empirically Derived Subtypes of Mild Cognitive Impairment. J Int Neuropsychol Soc 24:842-853
Graves, Lisa V; Van Etten, Emily J; Holden, Heather M et al. (2018) Refining CVLT-II recognition discriminability indices to enhance the characterization of recognition memory changes in healthy aging. Neuropsychol Dev Cogn B Aging Neuropsychol Cogn 25:767-782

Showing the most recent 10 out of 914 publications