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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”...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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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. |
format | Online Article Text |
id | pubmed-10463549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
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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