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Adaptive delivery of continuous and delayed feedback deep brain stimulation - a computational study
Adaptive deep brain stimulation (aDBS) is a closed-loop method, where high-frequency DBS is turned on and off according to a feedback signal, whereas conventional high-frequency DBS (cDBS) is delivered permanently. Using a computational model of subthalamic nucleus and external globus pallidus, we e...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646395/ https://www.ncbi.nlm.nih.gov/pubmed/31332226 http://dx.doi.org/10.1038/s41598-019-47036-4 |
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author | Popovych, Oleksandr V. Tass, Peter A. |
author_facet | Popovych, Oleksandr V. Tass, Peter A. |
author_sort | Popovych, Oleksandr V. |
collection | PubMed |
description | Adaptive deep brain stimulation (aDBS) is a closed-loop method, where high-frequency DBS is turned on and off according to a feedback signal, whereas conventional high-frequency DBS (cDBS) is delivered permanently. Using a computational model of subthalamic nucleus and external globus pallidus, we extend the concept of adaptive stimulation by adaptively controlling not only continuous, but also demand-controlled stimulation. Apart from aDBS and cDBS, we consider continuous pulsatile linear delayed feedback stimulation (cpLDF), specifically designed to induce desynchronization. Additionally, we combine adaptive on-off delivery with continuous delayed feedback modulation by introducing adaptive pulsatile linear delayed feedback stimulation (apLDF), where cpLDF is turned on and off using pre-defined amplitude thresholds. By varying the stimulation parameters of cDBS, aDBS, cpLDF, and apLDF we obtain optimal parameter ranges. We reveal a simple relation between the thresholds of the local field potential (LFP) for aDBS and apLDF, the extent of the stimulation-induced desynchronization, and the integral stimulation time required. We find that aDBS and apLDF can be more efficient in suppressing abnormal synchronization than continuous simulation. However, apLDF still remains more efficient and also causes a stronger reduction of the LFP beta burst length. Hence, adaptive on-off delivery may further improve the intrinsically demand-controlled pLDF. |
format | Online Article Text |
id | pubmed-6646395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66463952019-07-29 Adaptive delivery of continuous and delayed feedback deep brain stimulation - a computational study Popovych, Oleksandr V. Tass, Peter A. Sci Rep Article Adaptive deep brain stimulation (aDBS) is a closed-loop method, where high-frequency DBS is turned on and off according to a feedback signal, whereas conventional high-frequency DBS (cDBS) is delivered permanently. Using a computational model of subthalamic nucleus and external globus pallidus, we extend the concept of adaptive stimulation by adaptively controlling not only continuous, but also demand-controlled stimulation. Apart from aDBS and cDBS, we consider continuous pulsatile linear delayed feedback stimulation (cpLDF), specifically designed to induce desynchronization. Additionally, we combine adaptive on-off delivery with continuous delayed feedback modulation by introducing adaptive pulsatile linear delayed feedback stimulation (apLDF), where cpLDF is turned on and off using pre-defined amplitude thresholds. By varying the stimulation parameters of cDBS, aDBS, cpLDF, and apLDF we obtain optimal parameter ranges. We reveal a simple relation between the thresholds of the local field potential (LFP) for aDBS and apLDF, the extent of the stimulation-induced desynchronization, and the integral stimulation time required. We find that aDBS and apLDF can be more efficient in suppressing abnormal synchronization than continuous simulation. However, apLDF still remains more efficient and also causes a stronger reduction of the LFP beta burst length. Hence, adaptive on-off delivery may further improve the intrinsically demand-controlled pLDF. Nature Publishing Group UK 2019-07-22 /pmc/articles/PMC6646395/ /pubmed/31332226 http://dx.doi.org/10.1038/s41598-019-47036-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Popovych, Oleksandr V. Tass, Peter A. Adaptive delivery of continuous and delayed feedback deep brain stimulation - a computational study |
title | Adaptive delivery of continuous and delayed feedback deep brain stimulation - a computational study |
title_full | Adaptive delivery of continuous and delayed feedback deep brain stimulation - a computational study |
title_fullStr | Adaptive delivery of continuous and delayed feedback deep brain stimulation - a computational study |
title_full_unstemmed | Adaptive delivery of continuous and delayed feedback deep brain stimulation - a computational study |
title_short | Adaptive delivery of continuous and delayed feedback deep brain stimulation - a computational study |
title_sort | adaptive delivery of continuous and delayed feedback deep brain stimulation - a computational study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646395/ https://www.ncbi.nlm.nih.gov/pubmed/31332226 http://dx.doi.org/10.1038/s41598-019-47036-4 |
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