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Adaptive Deep Brain Stimulation In Advanced Parkinson Disease

Objective: Brain–computer interfaces (BCIs) could potentially be used to interact with pathological brain signals to intervene and ameliorate their effects in disease states. Here, we provide proof-of-principle of this approach by using a BCI to interpret pathological brain activity in patients with...

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Autores principales: Little, Simon, Pogosyan, Alex, Neal, Spencer, Zavala, Baltazar, Zrinzo, Ludvic, Hariz, Marwan, Foltynie, Thomas, Limousin, Patricia, Ashkan, Keyoumars, FitzGerald, James, Green, Alexander L, Aziz, Tipu Z, Brown, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3886292/
https://www.ncbi.nlm.nih.gov/pubmed/23852650
http://dx.doi.org/10.1002/ana.23951
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author Little, Simon
Pogosyan, Alex
Neal, Spencer
Zavala, Baltazar
Zrinzo, Ludvic
Hariz, Marwan
Foltynie, Thomas
Limousin, Patricia
Ashkan, Keyoumars
FitzGerald, James
Green, Alexander L
Aziz, Tipu Z
Brown, Peter
author_facet Little, Simon
Pogosyan, Alex
Neal, Spencer
Zavala, Baltazar
Zrinzo, Ludvic
Hariz, Marwan
Foltynie, Thomas
Limousin, Patricia
Ashkan, Keyoumars
FitzGerald, James
Green, Alexander L
Aziz, Tipu Z
Brown, Peter
author_sort Little, Simon
collection PubMed
description Objective: Brain–computer interfaces (BCIs) could potentially be used to interact with pathological brain signals to intervene and ameliorate their effects in disease states. Here, we provide proof-of-principle of this approach by using a BCI to interpret pathological brain activity in patients with advanced Parkinson disease (PD) and to use this feedback to control when therapeutic deep brain stimulation (DBS) is delivered. Our goal was to demonstrate that by personalizing and optimizing stimulation in real time, we could improve on both the efficacy and efficiency of conventional continuous DBS. Methods: We tested BCI-controlled adaptive DBS (aDBS) of the subthalamic nucleus in 8 PD patients. Feedback was provided by processing of the local field potentials recorded directly from the stimulation electrodes. The results were compared to no stimulation, conventional continuous stimulation (cDBS), and random intermittent stimulation. Both unblinded and blinded clinical assessments of motor effect were performed using the Unified Parkinson's Disease Rating Scale. Results: Motor scores improved by 66% (unblinded) and 50% (blinded) during aDBS, which were 29% (p = 0.03) and 27% (p = 0.005) better than cDBS, respectively. These improvements were achieved with a 56% reduction in stimulation time compared to cDBS, and a corresponding reduction in energy requirements (p < 0.001). aDBS was also more effective than no stimulation and random intermittent stimulation. Interpretation BCI-controlled DBS is tractable and can be more efficient and efficacious than conventional continuous neuromodulation for PD. Ann Neurol 2013;74:449–457
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spelling pubmed-38862922014-01-14 Adaptive Deep Brain Stimulation In Advanced Parkinson Disease Little, Simon Pogosyan, Alex Neal, Spencer Zavala, Baltazar Zrinzo, Ludvic Hariz, Marwan Foltynie, Thomas Limousin, Patricia Ashkan, Keyoumars FitzGerald, James Green, Alexander L Aziz, Tipu Z Brown, Peter Ann Neurol Original Articles Objective: Brain–computer interfaces (BCIs) could potentially be used to interact with pathological brain signals to intervene and ameliorate their effects in disease states. Here, we provide proof-of-principle of this approach by using a BCI to interpret pathological brain activity in patients with advanced Parkinson disease (PD) and to use this feedback to control when therapeutic deep brain stimulation (DBS) is delivered. Our goal was to demonstrate that by personalizing and optimizing stimulation in real time, we could improve on both the efficacy and efficiency of conventional continuous DBS. Methods: We tested BCI-controlled adaptive DBS (aDBS) of the subthalamic nucleus in 8 PD patients. Feedback was provided by processing of the local field potentials recorded directly from the stimulation electrodes. The results were compared to no stimulation, conventional continuous stimulation (cDBS), and random intermittent stimulation. Both unblinded and blinded clinical assessments of motor effect were performed using the Unified Parkinson's Disease Rating Scale. Results: Motor scores improved by 66% (unblinded) and 50% (blinded) during aDBS, which were 29% (p = 0.03) and 27% (p = 0.005) better than cDBS, respectively. These improvements were achieved with a 56% reduction in stimulation time compared to cDBS, and a corresponding reduction in energy requirements (p < 0.001). aDBS was also more effective than no stimulation and random intermittent stimulation. Interpretation BCI-controlled DBS is tractable and can be more efficient and efficacious than conventional continuous neuromodulation for PD. Ann Neurol 2013;74:449–457 Blackwell Publishing Ltd 2013-09 2013-07-12 /pmc/articles/PMC3886292/ /pubmed/23852650 http://dx.doi.org/10.1002/ana.23951 Text en Copyright © 2013 American Neurological Association http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons License, which permits use and distribution in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Little, Simon
Pogosyan, Alex
Neal, Spencer
Zavala, Baltazar
Zrinzo, Ludvic
Hariz, Marwan
Foltynie, Thomas
Limousin, Patricia
Ashkan, Keyoumars
FitzGerald, James
Green, Alexander L
Aziz, Tipu Z
Brown, Peter
Adaptive Deep Brain Stimulation In Advanced Parkinson Disease
title Adaptive Deep Brain Stimulation In Advanced Parkinson Disease
title_full Adaptive Deep Brain Stimulation In Advanced Parkinson Disease
title_fullStr Adaptive Deep Brain Stimulation In Advanced Parkinson Disease
title_full_unstemmed Adaptive Deep Brain Stimulation In Advanced Parkinson Disease
title_short Adaptive Deep Brain Stimulation In Advanced Parkinson Disease
title_sort adaptive deep brain stimulation in advanced parkinson disease
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3886292/
https://www.ncbi.nlm.nih.gov/pubmed/23852650
http://dx.doi.org/10.1002/ana.23951
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