Cargando…

A Pilot Study on Data-Driven Adaptive Deep Brain Stimulation in Chronically Implanted Essential Tremor Patients

Deep brain stimulation (DBS) is an established therapy for Parkinson's disease (PD) and essential-tremor (ET). In adaptive DBS (aDBS) systems, online tuning of stimulation parameters as a function of neural signals may improve treatment efficacy and reduce side-effects. State-of-the-art aDBS sy...

Descripción completa

Detalles Bibliográficos
Autores principales: Castaño-Candamil, Sebastián, Ferleger, Benjamin I., Haddock, Andrew, Cooper, Sarah S., Herron, Jeffrey, Ko, Andrew, Chizeck, Howard. J., Tangermann, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674800/
https://www.ncbi.nlm.nih.gov/pubmed/33250727
http://dx.doi.org/10.3389/fnhum.2020.541625
_version_ 1783611583953371136
author Castaño-Candamil, Sebastián
Ferleger, Benjamin I.
Haddock, Andrew
Cooper, Sarah S.
Herron, Jeffrey
Ko, Andrew
Chizeck, Howard. J.
Tangermann, Michael
author_facet Castaño-Candamil, Sebastián
Ferleger, Benjamin I.
Haddock, Andrew
Cooper, Sarah S.
Herron, Jeffrey
Ko, Andrew
Chizeck, Howard. J.
Tangermann, Michael
author_sort Castaño-Candamil, Sebastián
collection PubMed
description Deep brain stimulation (DBS) is an established therapy for Parkinson's disease (PD) and essential-tremor (ET). In adaptive DBS (aDBS) systems, online tuning of stimulation parameters as a function of neural signals may improve treatment efficacy and reduce side-effects. State-of-the-art aDBS systems use symptom surrogates derived from neural signals—so-called neural markers (NMs)—defined on the patient-group level, and control strategies assuming stationarity of symptoms and NMs. We aim at improving these aDBS systems with (1) a data-driven approach for identifying patient- and session-specific NMs and (2) a control strategy coping with short-term non-stationary dynamics. The two building blocks are implemented as follows: (1) The data-driven NMs are based on a machine learning model estimating tremor intensity from electrocorticographic signals. (2) The control strategy accounts for local variability of tremor statistics. Our study with three chronically implanted ET patients amounted to five online sessions. Tremor quantified from accelerometer data shows that symptom suppression is at least equivalent to that of a continuous DBS strategy in 3 out-of 4 online tests, while considerably reducing net stimulation (at least 24%). In the remaining online test, symptom suppression was not significantly different from either the continuous strategy or the no treatment condition. We introduce a novel aDBS system for ET. It is the first aDBS system based on (1) a machine learning model to identify session-specific NMs, and (2) a control strategy coping with short-term non-stationary dynamics. We show the suitability of our aDBS approach for ET, which opens the door to its further study in a larger patient population.
format Online
Article
Text
id pubmed-7674800
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-76748002020-11-27 A Pilot Study on Data-Driven Adaptive Deep Brain Stimulation in Chronically Implanted Essential Tremor Patients Castaño-Candamil, Sebastián Ferleger, Benjamin I. Haddock, Andrew Cooper, Sarah S. Herron, Jeffrey Ko, Andrew Chizeck, Howard. J. Tangermann, Michael Front Hum Neurosci Human Neuroscience Deep brain stimulation (DBS) is an established therapy for Parkinson's disease (PD) and essential-tremor (ET). In adaptive DBS (aDBS) systems, online tuning of stimulation parameters as a function of neural signals may improve treatment efficacy and reduce side-effects. State-of-the-art aDBS systems use symptom surrogates derived from neural signals—so-called neural markers (NMs)—defined on the patient-group level, and control strategies assuming stationarity of symptoms and NMs. We aim at improving these aDBS systems with (1) a data-driven approach for identifying patient- and session-specific NMs and (2) a control strategy coping with short-term non-stationary dynamics. The two building blocks are implemented as follows: (1) The data-driven NMs are based on a machine learning model estimating tremor intensity from electrocorticographic signals. (2) The control strategy accounts for local variability of tremor statistics. Our study with three chronically implanted ET patients amounted to five online sessions. Tremor quantified from accelerometer data shows that symptom suppression is at least equivalent to that of a continuous DBS strategy in 3 out-of 4 online tests, while considerably reducing net stimulation (at least 24%). In the remaining online test, symptom suppression was not significantly different from either the continuous strategy or the no treatment condition. We introduce a novel aDBS system for ET. It is the first aDBS system based on (1) a machine learning model to identify session-specific NMs, and (2) a control strategy coping with short-term non-stationary dynamics. We show the suitability of our aDBS approach for ET, which opens the door to its further study in a larger patient population. Frontiers Media S.A. 2020-11-05 /pmc/articles/PMC7674800/ /pubmed/33250727 http://dx.doi.org/10.3389/fnhum.2020.541625 Text en Copyright © 2020 Castaño-Candamil, Ferleger, Haddock, Cooper, Herron, Ko, Chizeck and Tangermann. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Human Neuroscience
Castaño-Candamil, Sebastián
Ferleger, Benjamin I.
Haddock, Andrew
Cooper, Sarah S.
Herron, Jeffrey
Ko, Andrew
Chizeck, Howard. J.
Tangermann, Michael
A Pilot Study on Data-Driven Adaptive Deep Brain Stimulation in Chronically Implanted Essential Tremor Patients
title A Pilot Study on Data-Driven Adaptive Deep Brain Stimulation in Chronically Implanted Essential Tremor Patients
title_full A Pilot Study on Data-Driven Adaptive Deep Brain Stimulation in Chronically Implanted Essential Tremor Patients
title_fullStr A Pilot Study on Data-Driven Adaptive Deep Brain Stimulation in Chronically Implanted Essential Tremor Patients
title_full_unstemmed A Pilot Study on Data-Driven Adaptive Deep Brain Stimulation in Chronically Implanted Essential Tremor Patients
title_short A Pilot Study on Data-Driven Adaptive Deep Brain Stimulation in Chronically Implanted Essential Tremor Patients
title_sort pilot study on data-driven adaptive deep brain stimulation in chronically implanted essential tremor patients
topic Human Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674800/
https://www.ncbi.nlm.nih.gov/pubmed/33250727
http://dx.doi.org/10.3389/fnhum.2020.541625
work_keys_str_mv AT castanocandamilsebastian apilotstudyondatadrivenadaptivedeepbrainstimulationinchronicallyimplantedessentialtremorpatients
AT ferlegerbenjamini apilotstudyondatadrivenadaptivedeepbrainstimulationinchronicallyimplantedessentialtremorpatients
AT haddockandrew apilotstudyondatadrivenadaptivedeepbrainstimulationinchronicallyimplantedessentialtremorpatients
AT coopersarahs apilotstudyondatadrivenadaptivedeepbrainstimulationinchronicallyimplantedessentialtremorpatients
AT herronjeffrey apilotstudyondatadrivenadaptivedeepbrainstimulationinchronicallyimplantedessentialtremorpatients
AT koandrew apilotstudyondatadrivenadaptivedeepbrainstimulationinchronicallyimplantedessentialtremorpatients
AT chizeckhowardj apilotstudyondatadrivenadaptivedeepbrainstimulationinchronicallyimplantedessentialtremorpatients
AT tangermannmichael apilotstudyondatadrivenadaptivedeepbrainstimulationinchronicallyimplantedessentialtremorpatients
AT castanocandamilsebastian pilotstudyondatadrivenadaptivedeepbrainstimulationinchronicallyimplantedessentialtremorpatients
AT ferlegerbenjamini pilotstudyondatadrivenadaptivedeepbrainstimulationinchronicallyimplantedessentialtremorpatients
AT haddockandrew pilotstudyondatadrivenadaptivedeepbrainstimulationinchronicallyimplantedessentialtremorpatients
AT coopersarahs pilotstudyondatadrivenadaptivedeepbrainstimulationinchronicallyimplantedessentialtremorpatients
AT herronjeffrey pilotstudyondatadrivenadaptivedeepbrainstimulationinchronicallyimplantedessentialtremorpatients
AT koandrew pilotstudyondatadrivenadaptivedeepbrainstimulationinchronicallyimplantedessentialtremorpatients
AT chizeckhowardj pilotstudyondatadrivenadaptivedeepbrainstimulationinchronicallyimplantedessentialtremorpatients
AT tangermannmichael pilotstudyondatadrivenadaptivedeepbrainstimulationinchronicallyimplantedessentialtremorpatients