Cargando…

DyNeuMo Mk-2: An Investigational Circadian-Locked Neuromodulator with Responsive Stimulation for Applied Chronobiology

Deep brain stimulation (DBS) for Parkinson’s disease, essential tremor and epilepsy is an established palliative treatment. DBS uses electrical neuromodulation to suppress symptoms. Most current systems provide a continuous pattern of fixed stimulation, with clinical follow-ups to refine settings co...

Descripción completa

Detalles Bibliográficos
Autores principales: Toth, Robert, Zamora, Mayela, Ottaway, Jon, Gillbe, Tom, Martin, Sean, Benjaber, Moaad, Lamb, Guy, Noone, Tara, Taylor, Barry, Deli, Alceste, Kremen, Vaclav, Worrell, Gregory, Constandinou, Timothy G., Gillbe, Ivor, De Wachter, Stefan, Knowles, Charles, Sharott, Andrew, Valentin, Antonio, Green, Alexander L., Denison, Timothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7116879/
https://www.ncbi.nlm.nih.gov/pubmed/33692611
http://dx.doi.org/10.1109/SMC42975.2020.9283187
_version_ 1783514253973520384
author Toth, Robert
Zamora, Mayela
Ottaway, Jon
Gillbe, Tom
Martin, Sean
Benjaber, Moaad
Lamb, Guy
Noone, Tara
Taylor, Barry
Deli, Alceste
Kremen, Vaclav
Worrell, Gregory
Constandinou, Timothy G.
Gillbe, Ivor
De Wachter, Stefan
Knowles, Charles
Sharott, Andrew
Valentin, Antonio
Green, Alexander L.
Denison, Timothy
author_facet Toth, Robert
Zamora, Mayela
Ottaway, Jon
Gillbe, Tom
Martin, Sean
Benjaber, Moaad
Lamb, Guy
Noone, Tara
Taylor, Barry
Deli, Alceste
Kremen, Vaclav
Worrell, Gregory
Constandinou, Timothy G.
Gillbe, Ivor
De Wachter, Stefan
Knowles, Charles
Sharott, Andrew
Valentin, Antonio
Green, Alexander L.
Denison, Timothy
author_sort Toth, Robert
collection PubMed
description Deep brain stimulation (DBS) for Parkinson’s disease, essential tremor and epilepsy is an established palliative treatment. DBS uses electrical neuromodulation to suppress symptoms. Most current systems provide a continuous pattern of fixed stimulation, with clinical follow-ups to refine settings constrained to normal office hours. An issue with this management strategy is that the impact of stimulation on circadian, i.e. sleep-wake, rhythms is not fully considered; either in the device design or in the clinical follow-up. Since devices can be implanted in brain targets that couple into the reticular activating network, impact on wakefulness and sleep can be significant. This issue will likely grow as new targets are explored, with the potential to create entraining signals that are uncoupled from environmental influences. To address this issue, we have designed a new brain-machine-interface for DBS that combines a slow-adaptive circadian-based stimulation pattern with a fast-acting pathway for responsive stimulation, demonstrated here for seizure management. In preparation for first-in-human research trials to explore the utility of multi-timescale automated adaptive algorithms, design and prototyping was carried out in line with ISO risk management standards, ensuring patient safety. The ultimate aim is to account for chronobiology within the algorithms embedded in brain-machine-interfaces and in neuromodulation technology more broadly.
format Online
Article
Text
id pubmed-7116879
institution National Center for Biotechnology Information
language English
publishDate 2020
record_format MEDLINE/PubMed
spelling pubmed-71168792021-03-09 DyNeuMo Mk-2: An Investigational Circadian-Locked Neuromodulator with Responsive Stimulation for Applied Chronobiology Toth, Robert Zamora, Mayela Ottaway, Jon Gillbe, Tom Martin, Sean Benjaber, Moaad Lamb, Guy Noone, Tara Taylor, Barry Deli, Alceste Kremen, Vaclav Worrell, Gregory Constandinou, Timothy G. Gillbe, Ivor De Wachter, Stefan Knowles, Charles Sharott, Andrew Valentin, Antonio Green, Alexander L. Denison, Timothy Conf Proc IEEE Int Conf Syst Man Cybern Article Deep brain stimulation (DBS) for Parkinson’s disease, essential tremor and epilepsy is an established palliative treatment. DBS uses electrical neuromodulation to suppress symptoms. Most current systems provide a continuous pattern of fixed stimulation, with clinical follow-ups to refine settings constrained to normal office hours. An issue with this management strategy is that the impact of stimulation on circadian, i.e. sleep-wake, rhythms is not fully considered; either in the device design or in the clinical follow-up. Since devices can be implanted in brain targets that couple into the reticular activating network, impact on wakefulness and sleep can be significant. This issue will likely grow as new targets are explored, with the potential to create entraining signals that are uncoupled from environmental influences. To address this issue, we have designed a new brain-machine-interface for DBS that combines a slow-adaptive circadian-based stimulation pattern with a fast-acting pathway for responsive stimulation, demonstrated here for seizure management. In preparation for first-in-human research trials to explore the utility of multi-timescale automated adaptive algorithms, design and prototyping was carried out in line with ISO risk management standards, ensuring patient safety. The ultimate aim is to account for chronobiology within the algorithms embedded in brain-machine-interfaces and in neuromodulation technology more broadly. 2020-10 2020-12-14 /pmc/articles/PMC7116879/ /pubmed/33692611 http://dx.doi.org/10.1109/SMC42975.2020.9283187 Text en https://creativecommons.org/licenses/by/4.0/ This paper was presented at the 2020 IEEE International Conference on Systems, Man, and Cybernetics, October 11th-14th 2020, Toronto, Canada. This is the accepted manuscript version of the article, released under a Creative Commons Attribution 4.0 License. For more information, refer to https://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Toth, Robert
Zamora, Mayela
Ottaway, Jon
Gillbe, Tom
Martin, Sean
Benjaber, Moaad
Lamb, Guy
Noone, Tara
Taylor, Barry
Deli, Alceste
Kremen, Vaclav
Worrell, Gregory
Constandinou, Timothy G.
Gillbe, Ivor
De Wachter, Stefan
Knowles, Charles
Sharott, Andrew
Valentin, Antonio
Green, Alexander L.
Denison, Timothy
DyNeuMo Mk-2: An Investigational Circadian-Locked Neuromodulator with Responsive Stimulation for Applied Chronobiology
title DyNeuMo Mk-2: An Investigational Circadian-Locked Neuromodulator with Responsive Stimulation for Applied Chronobiology
title_full DyNeuMo Mk-2: An Investigational Circadian-Locked Neuromodulator with Responsive Stimulation for Applied Chronobiology
title_fullStr DyNeuMo Mk-2: An Investigational Circadian-Locked Neuromodulator with Responsive Stimulation for Applied Chronobiology
title_full_unstemmed DyNeuMo Mk-2: An Investigational Circadian-Locked Neuromodulator with Responsive Stimulation for Applied Chronobiology
title_short DyNeuMo Mk-2: An Investigational Circadian-Locked Neuromodulator with Responsive Stimulation for Applied Chronobiology
title_sort dyneumo mk-2: an investigational circadian-locked neuromodulator with responsive stimulation for applied chronobiology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7116879/
https://www.ncbi.nlm.nih.gov/pubmed/33692611
http://dx.doi.org/10.1109/SMC42975.2020.9283187
work_keys_str_mv AT tothrobert dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT zamoramayela dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT ottawayjon dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT gillbetom dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT martinsean dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT benjabermoaad dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT lambguy dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT noonetara dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT taylorbarry dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT delialceste dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT kremenvaclav dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT worrellgregory dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT constandinoutimothyg dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT gillbeivor dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT dewachterstefan dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT knowlescharles dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT sharottandrew dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT valentinantonio dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT greenalexanderl dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology
AT denisontimothy dyneumomk2aninvestigationalcircadianlockedneuromodulatorwithresponsivestimulationforappliedchronobiology