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Subthalamic Nucleus Stimulation–Induced Local Field Potential Changes in Dystonia
Authors:Christoph Wiest MD  Francesca Morgante MD  PhD  Flavie Torrecillos PhD  Alek Pogosyan PhD  Shenghong He PhD  Fahd Baig MD  PhD  Ilaria Bertaina MD  Michael G. Hart MD  PhD  Mark J. Edwards MD  PhD  Erlick A. Pereira MD  Huiling Tan PhD
Affiliation:1. Medical Research Council Brain Network Dynamics Unit, Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom;2. Neurosciences Research Centre, Molecular and Clinical Sciences Institute, St. George's, University of London, London, United Kingdom;3. Medical Research Council Brain Network Dynamics Unit, Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom

Neurosciences Research Centre, Molecular and Clinical Sciences Institute, St. George's, University of London, London, United Kingdom;4. Institute of Psychiatry, Psychology and Neurosciences, King's College London, London, United Kingdom

Abstract:

Background

Subthalamic nucleus (STN) stimulation is an effective treatment for Parkinson's disease and induced local field potential (LFP) changes that have been linked with clinical improvement. STN stimulation has also been used in dystonia although the internal globus pallidus is the standard target where theta power has been suggested as a physiomarker for adaptive stimulation.

Objective

We aimed to explore if enhanced theta power was also present in STN and if stimulation-induced spectral changes that were previously reported for Parkinson's disease would occur in dystonia.

Methods

We recorded LFPs from 7 patients (12 hemispheres) with isolated craniocervical dystonia whose electrodes were placed such that inferior, middle, and superior contacts covered STN, zona incerta, and thalamus.

Results

We did not observe prominent theta power in STN at rest. STN stimulation induced similar spectral changes in dystonia as in Parkinson's disease, such as broadband power suppression, evoked resonant neural activity (ERNA), finely-tuned gamma oscillations, and an increase in aperiodic exponents in STN-LFPs. Both power suppression and ERNA localize to STN. Based on this, single-pulse STN stimulation elicits evoked neural activities with largest amplitudes in STN, which are relayed to the zona incerta and thalamus with changing characteristics as the distance from STN increases.

Conclusions

Our results show that STN stimulation–induced spectral changes are a nondisease-specific response to high-frequency stimulation, which can serve as placement markers for STN. This broadens the scope of STN stimulation and makes it an option for other disorders with excessive oscillatory peaks in STN. © 2022 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
Keywords:dystonia  deep brain stimulation  subthalamic nucleus  evoked resonant neural activity  local field potentials  finely tuned gamma oscillations
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