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Abstract Details

Neural Correlates of Impaired Motivation in Parkinson’s Disease
Movement Disorders
P2 - Poster Session 2 (5:30 PM-6:30 PM)
10-030

To improve our understanding of impaired motivation in Parkinson’s disease (PD), we tested the hypothesis that the neural basis of response to reward and penalty tasks lies within the prefrontal-basal ganglia circuitry.

Reduced motivation is common in PD. PD patients have decreased reactivity to positive (reward) and negative (penalty) signals, which contributes to their motivational disorder. We investigated the neural basis of motivation in patients with PD. 

Participants with PD (mean MOCA=25.5; disease duration=8.2 years; n=27) and demographically-matched controls (NC; mean MOCA=28.4.; n=16) completed a computerized task. We measured reaction time (RT) to press a target key in response to a stimulus presented on a computer screen. To assess motivation, participants were given an amount of money, and money is taken away as a “penalty” if they did not respond more rapidly to the stimulus relative to their previous performance. Participants also perform a “reward” condition where they received money for responding more rapidly. We related RTs on penalty and reward conditionsto volumetric imaging measures in 116 anatomically-defined regions of interest using linear regression models, adjusting for age, sex, total brain volume, and UPDRS-III. 

As expected, PD participants had slower latencies than NC on penalty (t[40]=3.56, p=0.0009) and reward conditions (t[34]=2.79, p=0.008). There were no significant differences in RT between penalty and reward conditions in PD participants. Penalty RT was related to atrophy in the orbitofrontal gyrus, putamen and thalamus. Reward RT was related to atrophy in orbitofrontal gyrus. 

Poor motivation may result from a lack of responsiveness to either reward or negative feedback. Frontal and subcortical regions important for processing this information may have specific roles for motivational functions. 

 

Authors/Disclosures
Lauren M. Massimo, PhD (University of PA, Neurology)
PRESENTER
No disclosure on file
Chinwe Nwadiogbu (University of Pennsylvania) No disclosure on file
Corey McMillan, PhD (University of Pennsylvania) Dr. McMillan has received personal compensation in the range of $500-$4,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for Elsevier. The institution of Dr. McMillan has received research support from Biogen. The institution of Dr. McMillan has received research support from NIH.
Nabila Dahodwala, MD, FAAN (Parkinson's disease and Movement Disorders Center) Dr. Dahodwala has received personal compensation in the range of $0-$499 for serving as a Consultant for Genetech. Dr. Dahodwala has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Mediflix. Dr. Dahodwala has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Acadia. Dr. Dahodwala has received personal compensation in the range of $5,000-$9,999 for serving as an Expert Witness for Post and Schell. Dr. Dahodwala has received personal compensation in the range of $10,000-$49,999 for serving as an Expert Witness for O'Brien & Ryan, LLP. Dr. Dahodwala has received personal compensation in the range of $10,000-$49,999 for serving as an Expert Witness for MotleyRice. The institution of Dr. Dahodwala has received research support from AbbVie. The institution of Dr. Dahodwala has received research support from Medtronic.