The Alzheimer's Disease Research Center (ADRC) Neuropathology Core has been completely reorganized during the present grant period. It provides state-of-the-art neuropathological examination of brains obtained from ADRC autopsy cases. Brains are processed in a standardized fashion, with detailed histopathological assessment, by means of examination of a standardized set of brain sections, now illustrated on our website. Standardized reports with extensive data are provided, including histopathological diagnoses using accepted neuropathological criteria and CERAD, NLA-Reagan, and Braak &Braak staging systems. The new procedures enhance the efficiency of the ADRC brain bank, and the value of collected brains to investigators whose specific research projects depend upon the availability of carefully prepared and examined tissue. Each ADRC brain is bisected, with one half formalin-fixed, and thoroughly examined neuropathologically. The other half is extensively dissected yielding up to 150 or more fresh frozen samples from precisely specified regions, harvested and processed at time of autopsy. Only trained neuropathologists perform the dissection to ensure consistency and accurate assessment of the tissue during the processing. The samples are categorized both diagnostically and qualitatively, electronically-tracked, ready for instant disbursement, and suitable for a wide range of investigations using various modern biochemical technologies. In addition to managing the collections of fresh frozen, and formalin-fixed brain samples, DNA and RNA samples are prepared and then stored from frozen brains, as is DNA from blood of living ADRC patients. The voluminous nature of the Neuropathology Core samples requires recording many crucial details. Thus, we have developed software that: (i) generates bar-code labels and tracks samples;(ii) pre-selects among thousand of samples those that best match the requirements of investigators according to the demographics and pathological changes;(iii) provides freezer cabinet coordinates for each sample;(iv) traces vacant freezer space after sample disbursements;and (v) registers recipient investigators. The Neuropathology Core actively supports numerous fertile interactions between neuroscientists, geneticists, clinicians and other AD researchers.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Specialized Center (P50)
Project #
5P50AG008702-20
Application #
7858435
Study Section
Special Emphasis Panel (ZAG1)
Project Start
Project End
Budget Start
2009-06-01
Budget End
2010-05-31
Support Year
20
Fiscal Year
2009
Total Cost
$218,349
Indirect Cost
Name
Columbia University (N.Y.)
Department
Type
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
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
Wang, Tingyan; Qiu, Robin G; Yu, Ming (2018) Predictive Modeling of the Progression of Alzheimer's Disease with Recurrent Neural Networks. Sci Rep 8:9161
Agogo, George O; Ramsey, Christine M; Gnjidic, Danijela et al. (2018) Longitudinal associations between different dementia diagnoses and medication use jointly accounting for dropout. Int Psychogeriatr 30:1477-1487
Alosco, Michael L; Sugarman, Michael A; Besser, Lilah M et al. (2018) A Clinicopathological Investigation of White Matter Hyperintensities and Alzheimer's Disease Neuropathology. J Alzheimers Dis 63:1347-1360
Brent, Robert J (2018) Estimating the monetary benefits of medicare eligibility for reducing the symptoms of dementia. Appl Econ 50:6327-6340
Deming, Yuetiva; Dumitrescu, Logan; Barnes, Lisa L et al. (2018) Sex-specific genetic predictors of Alzheimer's disease biomarkers. Acta Neuropathol 136:857-872
Winawer, Melodie R; Griffin, Nicole G; Samanamud, Jorge et al. (2018) Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy. Ann Neurol 83:1133-1146

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