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[18F]Flubatine: a Novel Biomarker of Cholinergic a4ß2 Nicotinic Receptors and Cognition in Parkinson's Disease
Mild cognitive impairment and dementia are frequent non-motor complications of moderate to advanced Parkinson's disease. Brain positron emission tomography (PET) study findings confirm post-mortem evidence that cholinergic loss is related to cognitive impairment in Parkinson's disease. However, current cholinergic augmentation therapy is not always effective and it should only target those Parkinson's disease patients who have evidence of cholinergic system impairment. The objective of this study is to study the association of a particular subtype of cholinergic receptors, so-called nicotinic acetylcholine receptors, with cognition in Parkinson's disease using a novel PET marker of cholinergic system integrity.
Parkinson's disease patients will undergo nicotinic acetylcholine receptor PET imaging with the radioligand \[18F\]flubatine and MRI on one day and extensive neuropsychological testing on another day. The degree of nicotinic receptor expression obtained with PET imaging will be correlated with the neuropsychology test results. Positive \[18F\]flubatine PET findings in this study would establish nicotinic receptors as an important contributor to cognitive dysfunction in Parkinson's disease and could kindle pharmaceutical interest in pursuing these agents for Parkinson's disease applications. We expect that lower nicotinic receptor expression is associated with impaired cognitive functioning in Parkinson's disease. In a personalized medicine approach the PET radioligand \[18F\]flubatine could serve as an important marker to identify those patients who are expected to benefit most from nicotinic receptor drug treatment.
Age
50 - No limit years
Sex
ALL
Healthy Volunteers
Yes
University of Michigan Health System
Ann Arbor, Michigan, United States
Start Date
February 1, 2014
Primary Completion Date
December 30, 2016
Completion Date
December 30, 2016
Last Updated
April 17, 2017
48
ACTUAL participants
Lead Sponsor
University of Michigan
Collaborators
NCT07310264
NCT02119611
Data Source & Attribution
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View ClinicalTrials.gov Terms and ConditionsNCT07216976