Evaluates passive monitoring of chorea in Huntington’s disease, suggesting improved assessment methods.
Chorea is a hallmark of Huntington’s disease (HD), yet its clinical assessment is of limited reliability, impairing our ability to sensitively evaluate its progression. We evaluated passive monitoring for estimating the two-year evolution of upper limb chorea in HD. Across four studies, 1025 participants collected smartwatch accelerometer data during their everyday life. We developed a machine learning model anchored to in-clinic upper limb chorea and trained cross-sectionally on disease-relevant features. The final model, selected using nested cross-validation, allowed estimating the longitudinal evolution of chorea. The resulting digital passive monitoring chorea score shows a progression of 0.13 points per year (95% CI: [0.08, 0.17]), and a robust sensitivity to change across studies, avoiding biases related to in-clinic measurements. High-resolution accelerometer data collected passively during daily life can improve the measurement of chorea in HD. Clinical Trial Registry Name: ClinicalTrials.gov; Study IDs: NCT03761849 registered 2018-11-30 and NCT03664804 registered 2018-09-07.
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