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Personalized chronic adaptive deep brain stimulation outperforms conventional stimulation in Parkinson’s disease

Deep brain stimulation is a widely used therapy for Parkinson’s disease (PD) but currently lacks dynamic responsiveness to changing clinical and neural states. Feedback control has the potential to improve therapeutic effectiveness, but optimal control strategy and additional benefits of “adaptive”...

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Autores principales: Oehrn, Carina R, Cernera, Stephanie, Hammer, Lauren H, Shcherbakova, Maria, Yao, Jiaang, Hahn, Amelia, Wang, Sarah, Ostrem, Jill L, Little, Simon, Starr, Philip A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463549/
https://www.ncbi.nlm.nih.gov/pubmed/37649907
http://dx.doi.org/10.1101/2023.08.03.23293450
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author Oehrn, Carina R
Cernera, Stephanie
Hammer, Lauren H
Shcherbakova, Maria
Yao, Jiaang
Hahn, Amelia
Wang, Sarah
Ostrem, Jill L
Little, Simon
Starr, Philip A
author_facet Oehrn, Carina R
Cernera, Stephanie
Hammer, Lauren H
Shcherbakova, Maria
Yao, Jiaang
Hahn, Amelia
Wang, Sarah
Ostrem, Jill L
Little, Simon
Starr, Philip A
author_sort Oehrn, Carina R
collection PubMed
description Deep brain stimulation is a widely used therapy for Parkinson’s disease (PD) but currently lacks dynamic responsiveness to changing clinical and neural states. Feedback control has the potential to improve therapeutic effectiveness, but optimal control strategy and additional benefits of “adaptive” neurostimulation are unclear. We implemented adaptive subthalamic nucleus stimulation, controlled by subthalamic or cortical signals, in three PD patients (five hemispheres) during normal daily life. We identified neurophysiological biomarkers of residual motor fluctuations using data-driven analyses of field potentials over a wide frequency range and varying stimulation amplitudes. Narrowband gamma oscillations (65–70 Hz) at either site emerged as the best control signal for sensing during stimulation. A blinded, randomized trial demonstrated improved motor symptoms and quality of life compared to clinically optimized standard stimulation. Our approach highlights the promise of personalized adaptive neurostimulation based on data-driven selection of control signals and may be applied to other neurological disorders.
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spelling pubmed-104635492023-08-30 Personalized chronic adaptive deep brain stimulation outperforms conventional stimulation in Parkinson’s disease Oehrn, Carina R Cernera, Stephanie Hammer, Lauren H Shcherbakova, Maria Yao, Jiaang Hahn, Amelia Wang, Sarah Ostrem, Jill L Little, Simon Starr, Philip A medRxiv Article Deep brain stimulation is a widely used therapy for Parkinson’s disease (PD) but currently lacks dynamic responsiveness to changing clinical and neural states. Feedback control has the potential to improve therapeutic effectiveness, but optimal control strategy and additional benefits of “adaptive” neurostimulation are unclear. We implemented adaptive subthalamic nucleus stimulation, controlled by subthalamic or cortical signals, in three PD patients (five hemispheres) during normal daily life. We identified neurophysiological biomarkers of residual motor fluctuations using data-driven analyses of field potentials over a wide frequency range and varying stimulation amplitudes. Narrowband gamma oscillations (65–70 Hz) at either site emerged as the best control signal for sensing during stimulation. A blinded, randomized trial demonstrated improved motor symptoms and quality of life compared to clinically optimized standard stimulation. Our approach highlights the promise of personalized adaptive neurostimulation based on data-driven selection of control signals and may be applied to other neurological disorders. Cold Spring Harbor Laboratory 2023-08-08 /pmc/articles/PMC10463549/ /pubmed/37649907 http://dx.doi.org/10.1101/2023.08.03.23293450 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Oehrn, Carina R
Cernera, Stephanie
Hammer, Lauren H
Shcherbakova, Maria
Yao, Jiaang
Hahn, Amelia
Wang, Sarah
Ostrem, Jill L
Little, Simon
Starr, Philip A
Personalized chronic adaptive deep brain stimulation outperforms conventional stimulation in Parkinson’s disease
title Personalized chronic adaptive deep brain stimulation outperforms conventional stimulation in Parkinson’s disease
title_full Personalized chronic adaptive deep brain stimulation outperforms conventional stimulation in Parkinson’s disease
title_fullStr Personalized chronic adaptive deep brain stimulation outperforms conventional stimulation in Parkinson’s disease
title_full_unstemmed Personalized chronic adaptive deep brain stimulation outperforms conventional stimulation in Parkinson’s disease
title_short Personalized chronic adaptive deep brain stimulation outperforms conventional stimulation in Parkinson’s disease
title_sort personalized chronic adaptive deep brain stimulation outperforms conventional stimulation in parkinson’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10463549/
https://www.ncbi.nlm.nih.gov/pubmed/37649907
http://dx.doi.org/10.1101/2023.08.03.23293450
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