Feasibility and utility of a simple computerized test for measuring saccade latency in progressive supranuclear palsy- a proof-of-concept study

• Published in: Journal of Clinical Movement Disorders (Online) Vol. 6; no. 1; p. 6
• Main Authors: Dale, Marian L., Scott, Emmi P., Khalid, Saher, Eiseman, Andrew S., Turner, Travis H.
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 06.12.2019; BioMed Central
• Subjects: Age; Analysis; Batteries; Discrimination; Eye examination; Eye movements; Future predictions; L-dopa; Measurement; Movement disorders; Parkinson's disease; Progressive supranuclear palsy; Ratings & rankings; Statistical analysis; Saccades; Progressive supranuclear palsy; Eye tracking
• ISSN: 2054-7072; 2054-7072
• DOI: 10.1186/s40734-019-0081-2

Reliable detection of slowed vertical saccades may help discriminate progressive supranuclear palsy (PSP) from the subset of Parkinson's disease patients who lack tremor (akinetic-rigid or PD-postural instability and gait disorder PIGD subtype), and from age-related oculomotor changes. We investigated the feasibility of a camera-less computerized behavioral saccade latency paradigm previously validated in PD to discriminate probable PSP-Richardson syndrome (PSP-RS) from PD-PIGD and age-matched controls. In this proof-of-concept case-control study, reflexive saccade latencies were measured in 5 subjects with probable PSP-RS, 5 subjects with PD-PIGD subtype, and 5 age-matched controls using the behavioral paradigm. The battery was repeated approximately one month later. All subjects were examined off levodopa by a movement disorders neurologist and by an ophthalmologist, who also performed a dilated eye exam. Vertical prosaccade latencies were longer in the PSP group (median = 903 ms) relative to PD (median = 268 ms) and control groups (median = 235 ms), with no overlap between groups (100% accuracy). PSP subjects also had larger vertical-horizontal discrepancies than comparison groups. Test-retest reliability for the behavioral saccade measures was good (interclass correlation coefficient = 0.948; 95% confidence interval [0.856, 0.982]), and the measures strongly correlated with clinical ratings. Computerized behavioral measurement of reflexive saccade latency is feasible in PSP, and potentially discriminates probable PSP-RS from the PD-PIGD subtype. Findings from this proof-of-concept study support utility of the approach for obtaining objective saccade metrics in clinical evaluations and for tracking change in future, larger trials of moderately advanced PSP. Future studies should also examine the behavioral paradigm in earlier presentations of PSP and other subtypes of PSP.