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Digital gait outcomes for autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): discriminative, convergent, and ecological validity in a multicenter study (PROSPAX)

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Beichert, Lukas
Ilg, Winfried
Kessler, Christoph
Traschuetz, Andreas
Reich, Selina
Santorelli, Filippo M.
Gagnon, Cynthia
Schuele, Rebecca
Synofzik, Matthis

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Publication Date

2024

Language

en

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Journal article

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Abstract

Background: With treatment trials on the horizon, this study aimed to identify candidate digital-motor gait outcomes for autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), capturable by wearable sensors with multicenter validity, and ideally also ecological validity during free walking outside laboratory settings. Methods: Cross-sectional multicenter study (four centers), with gait assessments in 36 subjects (18 ARSACS patients; 18 controls) using three body-worn sensors (Opal, APDM) in laboratory settings and free walking in public spaces. Sensor gait measures were analyzed for discriminative validity from controls, and for convergent (ie, clinical and patient relevance) validity by correlations with SPRSmobility (primary outcome) and Scale for the Assessment and Rating of Ataxia (SARA), Spastic Paraplegia Rating Scale (SPRS), and activities of daily living subscore of the Friedreich Ataxia Rating Scale (FARS-ADL) (exploratory outcomes). Results: Of 30 hypothesis-based digital gait measures, 14 measures discriminated ARSACS patients from controls with large effect sizes (|Cliff's delta| > 0.8) in laboratory settings, with strongest discrimination by measures of spatiotemporal variability Lateral Step Deviation (delta = 0.98), SPcmp (delta = 0.94), and Swing CV (delta = 0.93). Large correlations with the SPRSmobility were observed for Swing CV (Spearman's rho = 0.84), Speed (rho = -0.63), and Harmonic Ratio V (rho = -0.62). During supervised free walking in a public space, 11/30 gait measures discriminated ARSACS from controls with large effect sizes. Large correlations with SPRSmobility were here observed for Swing CV (rho = 0.78) and Speed (rho = -0.69), without reductions in effect sizes compared with laboratory settings. Conclusions: We identified a promising set of digital-motor candidate gait outcomes for ARSACS, applicable in multicenter settings, correlating with patient-relevant health aspects, and with high validity also outside laboratory settings, thus simulating real-life walking with higher ecological validity.

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Movement Disorders

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Wiley

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Clinical neurology

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