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Abstract Details

Gait Correlates of Cerebellar Cholinergic Denervation in Parkinson's Disease
Movement Disorders
S43 - Movement Disorders: Biomarkers, Mechanisms, and Pathophysiology (1:48 PM-2:00 PM)
005

The purpose of this cross-sectional study was to investigate the cholinergic denervation of the cerebellum and its contribution to specific domains of gait impairment in Parkinson disease (PD).

A mélange of disabling motor and non-motor manifestations frequently affects people with PD. One particularly disabling component of motor dysfunction is gait impairment that leads to falls, reduces quality of life and ultimately leads to residential care placement. Gait imbalance is a key contributor to morbidity and mortality in PD and does not respond well to traditional dopaminergic therapy. Most functional neuroimaging studies focus on nigrostriatal dopaminergic pathways and do not adequately explain gait impairments in PD. This suggests involvement of other neurotransmitter systems or brain regions beyond the nigrostriatal pathway and possibly new targets for imaging biomarkers. Our prior studies demonstrated altered cerebellar resting-state functional connectivity relate to gait and cognitive dysfunction in PD.

We conducted PET analysis with radioligand [18F]VAT targeting vesicular acetylcholine transporter (VAChT) contrasting cerebellar cholinergic activity in 64 people with PD and 41 age-matched healthy control participants. VAT nondisplaceable binding potential (BPND) was calculated using multilinear reference tissue model 2 (MRTM2) utilizing 10-110 minutes of PET scan data with optimized eroded white matter reference region. Comprehensive spatiotemporal gait measures were acquired with a GAITRite walkway for behavioral correlations.

The PD participants had significantly reduced VAChT expression in distinct cerebellar regions including hemispheric motor and cognitive lobules and midline vermis. The reduced cerebellar cholinergic activity (VAT BPND) correlated with key gait measures including step width, variability in step width and step time in PD participants after controlling for confounding variables.

These results demonstrate regional cholinergic denervation of the cerebellum in PD and its gait correlates. Our data reflects the potential of cerebellar cholinergic measures as a novel imaging biomarker of gait impairment in PD.

Authors/Disclosures
Baijayanta Maiti, MD, PhD (Washington University in St. Louis School of Medicine)
PRESENTER
The institution of Dr. Maiti has received research support from National Center for Advancing Translational Sciences of the NIH . The institution of Dr. Maiti has received research support from National Institute of Neurological Disorders and Stroke (NINDS) / NIH .
John L. O'Donnell, PhD Dr. O'Donnell has nothing to disclose.
Kerri S. Rawson, PhD The institution of Dr. Rawson has received research support from NCCIH. The institution of Dr. Rawson has received research support from NINDS.
aaron tanenbaum Mr. tanenbaum has nothing to disclose.
Abdulmunaim Eid, MD Dr. Eid has nothing to disclose.
Sarah Grossen Sarah Grossen has nothing to disclose.
john T. hood Mr. hood has nothing to disclose.
Meghan C. Campbell, PhD (Washington University in St. Louis) The institution of Meghan C. Campbell has received research support from NIH. The institution of Meghan C. Campbell has received research support from NIH. The institution of Meghan C. Campbell has received research support from McDonnell Center for Systems Neuroscience. The institution of Meghan C. Campbell has received research support from WUSM Radiology Department. The institution of Meghan C. Campbell has received research support from NIH. Meghan C. Campbell has received personal compensation in the range of $0-$499 for serving as a Grant Reviewer with Parkinson Foundation. Meghan C. Campbell has received personal compensation in the range of $500-$4,999 for serving as a Grant Reviewer with Department of Defense.
Gammon M. Earhart, PhD, PT The institution of Dr. Earhart has received research support from NIH.
Joel S. Perlmutter, MD, FAAN (Washington University in St. Louis) Dr. Perlmutter has received personal compensation in the range of $500-$4,999 for serving as an officer or member of the Board of Directors for CHDI. Dr. Perlmutter has received personal compensation in the range of $0-$499 for serving as an officer or member of the Board of Directors for Parkinson Study Group. Dr. Perlmutter has received personal compensation in the range of $500-$4,999 for serving as an Expert Witness for Wood, Cooper and Peterson, LLC . Dr. Perlmutter has received personal compensation in the range of $500-$4,999 for serving as an Expert Witness for Simmons and Simmons LLP . The institution of Dr. Perlmutter has received research support from NIH. The institution of Dr. Perlmutter has received research support from American Parkinson Disease Association (Advanced Research Center at Washington University). The institution of Dr. Perlmutter has received research support from CHDI. The institution of Dr. Perlmutter has received research support from Huntington Disease Society of America. The institution of Dr. Perlmutter has received research support from University of Western Toronto. The institution of Dr. Perlmutter has received research support from Barnes-Jewish Hospital Foundation. The institution of Dr. Perlmutter has received research support from Michael J Fox Foundation. The institution of Dr. Perlmutter has received research support from UCSD. The institution of Dr. Perlmutter has received research support from Paula & Rodger Riney FUnd. The institution of Dr. Perlmutter has received research support from Jo Oertli Fund. The institution of Dr. Perlmutter has received research support from Murphy FUnd. The institution of Dr. Perlmutter has received research support from Fixel Fund. The institution of Dr. Perlmutter has received research support from N Grant WIlliams Fund. The institution of Dr. Perlmutter has received research support from Pohlman Fund. Dr. Perlmutter has received personal compensation in the range of $500-$4,999 for serving as a lecturer with Boston University. Dr. Perlmutter has received personal compensation in the range of $500-$4,999 for serving as a external advisor with Stanford University. Dr. Perlmutter has received personal compensation in the range of $500-$4,999 for serving as a visiting professor with Beth Israel Hospital. Dr. Perlmutter has received personal compensation in the range of $500-$4,999 for serving as a visiting professor with U Pennsylvania.