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Abstract Details

Psychomotor Vigilance in Lewy Body Diseases: Comparative Performance and Association With Core Features
Movement Disorders
P11 - Poster Session 11 (11:45 AM-12:45 PM)
17-003

Characterize Psychomotor Vigilance Task (PVT) performance across the Lewy body disease (LBD) spectrum (Parkinson’s disease (PD), PD dementia (PDD), and dementia with Lewy bodies (DLB)) and examine associations between PVT metrics and core disease features.

The cognitive impairment associated with LBD is often associated with impairment in tasks of sustained attention. The PVT and the NASA-PVT, a modified form adapted for touchscreen administration, are validated measures of sustained attention. The performance of the NASA-PVT in LBD and its associations with core clinical features have not previously been reported.

We assessed NASA-PVT performance for 5 minutes and derived mean reaction time (RT), mean reciprocal RT (RRT), RT variability defined as the standard deviation of RT, lapses defined as RT>500ms, slowest 10% RRT, and fastest 10% RT. Clinical measures included the Montreal Cognitive Assessment (MoCA), MDS Unified Parkinson’s Disease Rating Scale (MDS-UPDRS), Northeast Visual Hallucination Inventory, and Clinician Assessment of Fluctuations. Group differences were assessed using the Kruskal-Wallis test for continuous variables with Dunn’s post hoc tests for pairwise comparisons. Spearman correlation tests were used for correlation analyses.

PDD (n=17) and DLB (n=18) exhibited significantly slower mean RT, greater RT variability, and more lapses than HC (n=9) and PD (n=19, all p < .05). LBD participants with cognitive fluctuations showed significantly greater RT variability (p = .006) and reduced slowest 10% RRT (p = .027). Mean RT, RT variability, number of lapses, and slowest 10% RRT were significantly correlated with MoCA score, MDS-UPDRS Part 3, visual hallucination burden, and daytime sleepiness (all p<0.05).

Psychomotor vigilance is impaired in PDD and DLB compared to PD and HC. The correlation of impaired psychomotor vigilance with global cognition, cognitive fluctuations, visual hallucinations, and greater sleepiness supports a shared underlying mechanism across these clinical features in LBD.

Authors/Disclosures
Razan Hallak, MD
PRESENTER
Dr. Hallak has nothing to disclose.
Ahmed Negida, MD, PhD (Virginia Commonwealth University) Dr. Negida has nothing to disclose.
Madison Clemons, Clinical Research Coordinator Ms. Clemons has nothing to disclose.
Brian Berman, MD, MS, FAAN (Virginia Commonwealth University) The institution of Dr. Berman has received research support from Dystonia Medical Research Foundation. The institution of Dr. Berman has received research support from National Institutes of Health. The institution of Dr. Berman has received research support from Neurocrine Biosciences. The institution of Dr. Berman has received research support from Benign Essential Blepharospasm Research Foundation. The institution of Dr. Berman has received research support from National Institutes of Health.
Nitai Mukhopadhyay (Virginia Commonwealth University) Nitai Mukhopadhyay has nothing to disclose.
Matthew J. Barrett, MD, FAAN (Virginia Commonwealth University) The institution of Dr. Barrett has received research support from Kyowa Kirin. The institution of Dr. Barrett has received research support from NIH.