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Updated: Aug 6, 2026

Dynamic Digital Biomarkers of Motor and Cognitive Function in Parkinson's Disease
Published on: July 24, 2019
Device-embedded accelerometry complements neural signals for tracking parkinsonian motor states
Tao Liu1,2, Jiaang Yao3,4, Bahman Abdi-Sargezeh1,2
1MRC Centre of Research Excellence in Restorative Neural Dynamics, University of Oxford, Oxford, UK.
Device accelerometers accurately track Parkinson's motor state during deep brain stimulation (DBS). Accelerometry outperforms neural biomarkers, offering a robust solution for adaptive DBS systems.
Area of Science:
- Neuroscience
- Biomedical Engineering
- Neurology
Background:
- Adaptive deep brain stimulation (aDBS) uses physiological biomarkers to adjust therapy for Parkinson's disease (PD).
- Neural biomarkers may be affected by stimulation, impacting closed-loop control accuracy.
- Current methods for tracking PD motor state during aDBS require improvement.
Purpose of the Study:
- To evaluate the efficacy of device-embedded accelerometers in tracking Parkinsonian motor state during continuous subthalamic nucleus (STN) deep brain stimulation (DBS).
- To compare the performance of accelerometry-derived features against neural biomarkers for decoding motor symptoms under stimulation.
- To identify robust biomarkers for next-generation adaptive DBS systems.
Main Methods:
- Analysis of over 1,900 hours of chronic recordings including STN neural activity, cortical activity, and device-embedded accelerometry.
- Simultaneous recording of continuous wearable assessments for bradykinesia and dyskinesia.
- Comparison of motor symptom decoding accuracy using accelerometry-derived features versus neural features across different stimulation conditions.
Main Results:
- Accelerometry-derived features robustly tracked motor symptom severity (bradykinesia and dyskinesia) across all stimulation conditions.
- Accelerometry outperformed neural features, particularly STN beta power, in decoding motor state.
- STN beta power's utility was limited by conflating periodic and aperiodic neural processes, with periodic activity showing reduced coupling to symptoms under stimulation.
Conclusions:
- Device-embedded accelerometry provides a robust and stable behavioral biomarker for tracking Parkinson's motor state during deep brain stimulation.
- Neural biomarkers, like STN beta power, exhibit differential robustness and may be less reliable under active stimulation.
- Accelerometry is a promising candidate biomarker for enhancing the performance and reliability of future adaptive DBS systems.
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