Real-life ankle submovements and computer mouse use reflect patient-reported function in adult ataxias

Nicole M Eklund, Jessey Ouillon, Vineet Pandey, Christopher D Stephen, Jeremy D Schmahmann, Jeremy Edgerton, Krzysztof Z Gajos, and Anoopum S Gupta


 


Abstract

{Novel disease modifying therapies are being evaluated in spinocerebellar ataxias and multiple system atrophy. Clinician-performed disease rating scales are relatively insensitive for measuring disease change over time, resulting in large and long clinical trials. We tested the hypothesis that sensors worn continuously at home during natural behavior and a web-based computer mouse task performed at home could produce interpretable, meaningful, and reliable motor measures for potential use in clinical trials.Thirty-four individuals with degenerative ataxias (spinocerebellar ataxia types 1, 2, 3, and 6 and multiple system atrophy of the cerebellar type) and eight age-matched controls completed the cross-sectional study. Participants wore an ankle and wrist sensor continuously at-home for one week and completed the Hevelius computer mouse task eight times over four weeks. We examined properties of motor primitives called ``submovements'' derived from the continuous wearable sensors and properties of computer mouse clicks and trajectories in relationship to patient-reported measures of function (PROM-Ataxia) and ataxia rating scales (Scale for the Assessment and Rating of Ataxia and the Brief Ataxia Rating Scale). The test-retest reliability of digital measures and differences between ataxia and control participants were evaluated.Individuals with ataxia had smaller, slower, and less powerful ankle submovements during natural behavior at home. A composite measure based on ankle submovements strongly correlated with ataxia rating scale scores (Pearson's r = 0.82-0.88), strongly correlated with self-reported function (r = 0.81), had high test-retest reliability (intraclass correlation coefficient = 0.95), and distinguished ataxia and control participants, including preataxic individuals (N=4) from controls. A composite measure based on computer mouse movements and clicks strongly correlated with ataxia rating scale total (r = 0.86-0.88) and arm scores (r = 0.65-0.75), correlated well with self-reported function (r = 0.72-0.73), and had high test-retest reliability (intraclass correlation coefficient = 0.99).These data indicate that interpretable, meaningful, and highly reliable motor measures can be obtained from continuous measurement of natural movement, particularly at the ankle location, and from computer mouse movements during a simple point-and-click task performed at home. This study supports the use of these two inexpensive and easy-to-use technologies in longitudinal natural history studies in spinocerebellar ataxias and multiple system atrophy of the cerebellar type and shows promise as potential motor outcome measures in interventional trials.}

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Citation Information

Nicole M Eklund, Jessey Ouillon, Vineet Pandey, Christopher D Stephen, Jeremy D Schmahmann, Jeremy Edgerton, Krzysztof Z Gajos, and Anoopum S Gupta. Real-life ankle submovements and computer mouse use reflect patient-reported function in adult ataxias. Brain Communications, 5(2), 03 2023.

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