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Updated: May 14, 2026

Controlling Parkinson's Disease With Adaptive Deep Brain Stimulation
Published on: July 16, 2014
Dynamic neural states underpin motor symptom severity in Parkinson's disease: a longitudinal analysis of chronic
Abhinav Sharma1, Tao Liu1, Bahman Abdi-Sargezeh1
1Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom; MRC Brain Networks Dynamics Unit, University of Oxford, Oxford, United Kingdom.
Background:
Motor symptoms in Parkinson's disease (PD) may arise due to transient, network-wide neural dynamics that extend beyond beta-band oscillatory activity within the motor cortical-subthalamic nucleus (STN) circuit.
Methods:
We applied a four-state Hidden Markov Model (HMM) to identify states of local and interregional oscillatory synchrony from chronic motor cortical and STN recordings (1046 h from 10 hemispheres) in five patients with PD (mean age 49 years), with concurrent measurements of bradykinesia, dyskinesia and tremor quantified using wearable sensors.
Findings:
Neural states exhibited distinct spectral and temporal features relating to symptom severity. Two states exhibited spectral signatures-particularly STN low and high gamma, STN delta/alpha, cortical beta, and cortico-STN beta coherence-that predicted worsening bradykinesia. STN beta oscillations were not consistent predictors of bradykinesia (p = 0.52), but did predict worsening tremor (p < 0.01) and also improvements in dyskinesia severity (p < 0.001), in a state specific manner. These states also displayed compensatory features associated with bradykinesia amelioration, including cortical delta/alpha activity, cortical high gamma, and cortico-STN high gamma coherence. Additionally, we identified a state, marked by STN beta without cortico-STN beta coherence, whose increased lifetimes and occurrence improved motor function (p < 0.001).
Interpretation:
Our findings highlight the multidimensional nature of motor impairments in PD and suggest that adaptive interventions targeting state features-rather than single frequency bands-may offer new opportunities for personalised neuromodulation.
Funding:
AO: MRC Clinician Scientist Fellowship (MR/W024810/1), Rosetrees Trust/Race Against Dementia Team award, Oxford Hospitals Charity, and the Jon Moulton Charity Trust. TL: China Scholarship Council.
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