The Neuropathology Core serves a number of critical functions within the ADRC. It has and will continue to serve to prove the facilities, expertise and personnel to obtain brain specimens from well characterized elderly demented subjects (primarily suffering from Alzheimer's disease) as well as elderly control subjects. The Neuropathology Core provides 24 hour coverage by trained prosectors and has achieved an enviable record of short post-mortem intervals (mean post-mortem interval 282.9 + 162.6 minutes). To date, a total of 231 brains have been processed through the ADRC brain bank. Each brain specimen is subjected to a detailed dissection protocol which is specifically designed to provide optimally handled and preserved specimens for all of the researchers involved in the ADRC as well as other colleagues and collaborators involved in AD-related research. Each specimen undergoes a detailed neuropathology work-up in which the nature and extent of neuropathologic lesions present are evaluated and documented and a diagnostic neuropatholgic report is issued. The brain tissues obtained are actively used in the ADRC's research efforts and data obtained from these samples have resulted in many important scientific findings and a large number of publications. We have made a conscious decision to concentrate our efforts on obtaining brains from patients on whom detailed and reliable clinical information is available. Accordingly, we have been able to engage in studies which correlate the extent and distribution of certain neuropathologic lesions with clinical aspects of V disease as well as with neurochemical parameters. We have achieved an excellent autopsy record for longitudinally followed ADRC patients (68% of deaths of longitudinally followed ADRC patients have been autopsied). In order to achieve an even higher autopsy rate, we have introduced a procedure in which the next-of-kin is asked to declare an intent to consent to autopsy well in advance of the death of the patient. Due to the chronic nature of this disease, we anticipate that a large number of our longitudinally followed ADRC patients will die within the upcoming funding period and feel that our efforts in seeking intents to consent to autopsy will result in our obtaining many additional valuable specimens. The Neuropathology Core continues to play a central role in the success of this ADRC.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Specialized Center (P50)
Project #
5P50AG005138-12
Application #
3726299
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
12
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Mount Sinai School of Medicine
Department
Type
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10029
Wang, Jen-Chyong; Alinaghi, Somayeh; Tafakhori, Abbas et al. (2018) Genetic screening in two Iranian families with early-onset Alzheimer's disease identified a novel PSEN1 mutation. Neurobiol Aging 62:244.e15-244.e17
Crum, Jana; Wilson, Jeffrey; Sabbagh, Marwan (2018) Does taking statins affect the pathological burden in autopsy-confirmed Alzheimer's dementia? Alzheimers Res Ther 10:104
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
Burke, Shanna L; Cadet, Tamara; Maddux, Marlaina (2018) Chronic Health Illnesses as Predictors of Mild Cognitive Impairment Among African American Older Adults. J Natl Med Assoc 110:314-325
Girdhar, Kiran; Hoffman, Gabriel E; Jiang, Yan et al. (2018) Cell-specific histone modification maps in the human frontal lobe link schizophrenia risk to the neuronal epigenome. Nat Neurosci 21:1126-1136
Kamara, Dennis M; Gangishetti, Umesh; Gearing, Marla et al. (2018) Cerebral Amyloid Angiopathy: Similarity in African-Americans and Caucasians with Alzheimer's Disease. J Alzheimers Dis 62:1815-1826
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
Huang, Qian; Voloudakis, Georgios; Ren, Yimin et al. (2018) Presenilin1/?-secretase protects neurons from glucose deprivation-induced death by regulating miR-212 and PEA15. FASEB J 32:243-253
Hauberg, Mads E; Fullard, John F; Zhu, Lingxue et al. (2018) Differential activity of transcribed enhancers in the prefrontal cortex of 537 cases with schizophrenia and controls. Mol Psychiatry :
Giambartolomei, Claudia; Zhenli Liu, Jimmy; Zhang, Wen et al. (2018) A Bayesian framework for multiple trait colocalization from summary association statistics. Bioinformatics 34:2538-2545

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