The Clinical Core (Core B) of the Penn Udall Center has four key functions: 1) To recruit patients with Parkinson's disease (PD), PD with dementia (PDD) dementia with Lewy bodies (DLB), and normal control subjects for the Udall Center's projects; 2) To develop strategies for outreach to minorities and recruit them for participation in studies; 3) To collaborate with the Administrative and Educational Core (Core A) in educating residents and fellows, health care professionals and the PD community; 4) to collaborate with the Statistical Core (Core D) to maintain a secure, compliant, state-of-the-art relational database; and 5) to join with the Neuropathology, Biomarker and Genetics Core (Core C) in collaboration with other Udall Centers on clinical characterization and sample collection. Patients and controls recruited to Core B will consent to donate blood and cerebrospinal fluid (CSF) during life, and brain tissue at death, for the identification of potential biomarkers of PD-related neurodegeneration, including peripheral biochemical analytes and genetic markers in blood and CSF. Participants in the Penn Udall Cohort will have annual evaluations to the time of death. The principal source of patients is the Parkinson's disease and Movement Disorders Center (PD&MDC) of the University of Pennsylvania, located at the Penn Neurological Institute at Pennsylvania Hospital. The PD&MDC is one of the largest referral sites in the northeastern US for the diagnosis and treatment of PD and other movement disorders.

Public Health Relevance

Parkinson's disease (PD) is a common neurodegenerative disease affecting approximately 1 million Americans. While the motor symptoms of PD are well-recognized and can be targeted by effective symptomatic medications, cognitive impairment and dementia in PD are common (affecting 80% of patients with PD for 20 years), costly, and without effective symptomatic therapies. Core B is essential to the success of the Projects of this application and to all collaborations described herein between the Penn Udall Center and other Udall Centers. Thus, Core B is the central clearing house for research that might lead to more meaningful therapies for cognitive impairment in PD.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Specialized Center (P50)
Project #
5P50NS053488-09
Application #
8900359
Study Section
Special Emphasis Panel (ZNS1-SRB-J)
Project Start
Project End
2016-06-30
Budget Start
2015-07-01
Budget End
2016-06-30
Support Year
9
Fiscal Year
2015
Total Cost
$330,002
Indirect Cost
$123,751
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Portelius, Erik; Olsson, Bob; Höglund, Kina et al. (2018) Cerebrospinal fluid neurogranin concentration in neurodegeneration: relation to clinical phenotypes and neuropathology. Acta Neuropathol 136:363-376
Polinski, Nicole K; Volpicelli-Daley, Laura A; Sortwell, Caryl E et al. (2018) Best Practices for Generating and Using Alpha-Synuclein Pre-Formed Fibrils to Model Parkinson's Disease in Rodents. J Parkinsons Dis 8:303-322
Rey, Nolwen L; George, Sonia; Steiner, Jennifer A et al. (2018) Spread of aggregates after olfactory bulb injection of ?-synuclein fibrils is associated with early neuronal loss and is reduced long term. Acta Neuropathol 135:65-83
Lewczuk, Piotr; Riederer, Peter; O'Bryant, Sid E et al. (2018) Cerebrospinal fluid and blood biomarkers for neurodegenerative dementias: An update of the Consensus of the Task Force on Biological Markers in Psychiatry of the World Federation of Societies of Biological Psychiatry. World J Biol Psychiatry 19:244-328
Simuni, Tanya; Caspell-Garcia, Chelsea; Coffey, Christopher S et al. (2018) Baseline prevalence and longitudinal evolution of non-motor symptoms in early Parkinson's disease: the PPMI cohort. J Neurol Neurosurg Psychiatry 89:78-88
Alcolea, Daniel; Irwin, David J; Illán-Gala, Ignacio et al. (2018) Elevated YKL-40 and low sAPP?:YKL-40 ratio in antemortem cerebrospinal fluid of patients with pathologically confirmed FTLD. J Neurol Neurosurg Psychiatry :
Luna, Esteban; Decker, Samantha C; Riddle, Dawn M et al. (2018) Differential ?-synuclein expression contributes to selective vulnerability of hippocampal neuron subpopulations to fibril-induced toxicity. Acta Neuropathol 135:855-875
Zee, Jarcy; Xie, Sharon X (2018) The Kaplan-Meier Method for Estimating and Comparing Proportions in a Randomized Controlled Trial with Dropouts. Biostat Epidemiol 2:23-33
Peng, Chao; Gathagan, Ronald J; Covell, Dustin J et al. (2018) Cellular milieu imparts distinct pathological ?-synuclein strains in ?-synucleinopathies. Nature 557:558-563
Weintraub, Daniel; Tröster, Alexander I; Marras, Connie et al. (2018) Initial cognitive changes in Parkinson's disease. Mov Disord 33:511-519

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