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Magnetoencephalography to measure the effect of contact point-specific deep brain stimulation in Parkinson’s disease: A proof of concept study

BACKGROUND: Deep brain stimulation (DBS) of the subthalamic nucleus (STN) is an effective treatment for disabling fluctuations in motor symptoms in Parkinson’s disease (PD) patients. However, iterative exploration of all individual contact points (four in each STN) by the clinician for optimal clini...

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Autores principales: Boon, Lennard I., Potters, Wouter V., Hillebrand, Arjan, de Bie, Rob M.A., Bot, Maarten, Richard Schuurman, P., van den Munckhof, Pepijn, Twisk, Jos W., Stam, Cornelis J., Berendse, Henk W., van Rootselaar, Anne-Fleur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197095/
https://www.ncbi.nlm.nih.gov/pubmed/37187041
http://dx.doi.org/10.1016/j.nicl.2023.103431
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author Boon, Lennard I.
Potters, Wouter V.
Hillebrand, Arjan
de Bie, Rob M.A.
Bot, Maarten
Richard Schuurman, P.
van den Munckhof, Pepijn
Twisk, Jos W.
Stam, Cornelis J.
Berendse, Henk W.
van Rootselaar, Anne-Fleur
author_facet Boon, Lennard I.
Potters, Wouter V.
Hillebrand, Arjan
de Bie, Rob M.A.
Bot, Maarten
Richard Schuurman, P.
van den Munckhof, Pepijn
Twisk, Jos W.
Stam, Cornelis J.
Berendse, Henk W.
van Rootselaar, Anne-Fleur
author_sort Boon, Lennard I.
collection PubMed
description BACKGROUND: Deep brain stimulation (DBS) of the subthalamic nucleus (STN) is an effective treatment for disabling fluctuations in motor symptoms in Parkinson’s disease (PD) patients. However, iterative exploration of all individual contact points (four in each STN) by the clinician for optimal clinical effects may take months. OBJECTIVE: In this proof of concept study we explored whether magnetoencephalography (MEG) has the potential to noninvasively measure the effects of changing the active contact point of STN-DBS on spectral power and functional connectivity in PD patients, with the ultimate aim to aid in the process of selecting the optimal contact point, and perhaps reduce the time to achieve optimal stimulation settings. METHODS: The study included 30 PD patients who had undergone bilateral DBS of the STN. MEG was recorded during stimulation of each of the eight contact points separately (four on each side). Each stimulation position was projected on a vector running through the longitudinal axis of the STN, leading to one scalar value indicating a more dorsolateral or ventromedial contact point position. Using linear mixed models, the stimulation positions were correlated with band-specific absolute spectral power and functional connectivity of i) the motor cortex ipsilateral tot the stimulated side, ii) the whole brain. RESULTS: At group level, more dorsolateral stimulation was associated with lower low-beta absolute band power in the ipsilateral motor cortex (p = .019). More ventromedial stimulation was associated with higher whole-brain absolute delta (p = .001) and theta (p = .005) power, as well as higher whole-brain theta band functional connectivity (p = .040). At the level of the individual patient, switching the active contact point caused significant changes in spectral power, but the results were highly variable. CONCLUSIONS: We demonstrate for the first time that stimulation of the dorsolateral (motor) STN in PD patients is associated with lower low-beta power values in the motor cortex. Furthermore, our group-level data show that the location of the active contact point correlates with whole-brain brain activity and connectivity. As results in individual patients were quite variable, it remains unclear if MEG is useful in the selection of the optimal DBS contact point.
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spelling pubmed-101970952023-05-20 Magnetoencephalography to measure the effect of contact point-specific deep brain stimulation in Parkinson’s disease: A proof of concept study Boon, Lennard I. Potters, Wouter V. Hillebrand, Arjan de Bie, Rob M.A. Bot, Maarten Richard Schuurman, P. van den Munckhof, Pepijn Twisk, Jos W. Stam, Cornelis J. Berendse, Henk W. van Rootselaar, Anne-Fleur Neuroimage Clin Regular Article BACKGROUND: Deep brain stimulation (DBS) of the subthalamic nucleus (STN) is an effective treatment for disabling fluctuations in motor symptoms in Parkinson’s disease (PD) patients. However, iterative exploration of all individual contact points (four in each STN) by the clinician for optimal clinical effects may take months. OBJECTIVE: In this proof of concept study we explored whether magnetoencephalography (MEG) has the potential to noninvasively measure the effects of changing the active contact point of STN-DBS on spectral power and functional connectivity in PD patients, with the ultimate aim to aid in the process of selecting the optimal contact point, and perhaps reduce the time to achieve optimal stimulation settings. METHODS: The study included 30 PD patients who had undergone bilateral DBS of the STN. MEG was recorded during stimulation of each of the eight contact points separately (four on each side). Each stimulation position was projected on a vector running through the longitudinal axis of the STN, leading to one scalar value indicating a more dorsolateral or ventromedial contact point position. Using linear mixed models, the stimulation positions were correlated with band-specific absolute spectral power and functional connectivity of i) the motor cortex ipsilateral tot the stimulated side, ii) the whole brain. RESULTS: At group level, more dorsolateral stimulation was associated with lower low-beta absolute band power in the ipsilateral motor cortex (p = .019). More ventromedial stimulation was associated with higher whole-brain absolute delta (p = .001) and theta (p = .005) power, as well as higher whole-brain theta band functional connectivity (p = .040). At the level of the individual patient, switching the active contact point caused significant changes in spectral power, but the results were highly variable. CONCLUSIONS: We demonstrate for the first time that stimulation of the dorsolateral (motor) STN in PD patients is associated with lower low-beta power values in the motor cortex. Furthermore, our group-level data show that the location of the active contact point correlates with whole-brain brain activity and connectivity. As results in individual patients were quite variable, it remains unclear if MEG is useful in the selection of the optimal DBS contact point. Elsevier 2023-05-10 /pmc/articles/PMC10197095/ /pubmed/37187041 http://dx.doi.org/10.1016/j.nicl.2023.103431 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Boon, Lennard I.
Potters, Wouter V.
Hillebrand, Arjan
de Bie, Rob M.A.
Bot, Maarten
Richard Schuurman, P.
van den Munckhof, Pepijn
Twisk, Jos W.
Stam, Cornelis J.
Berendse, Henk W.
van Rootselaar, Anne-Fleur
Magnetoencephalography to measure the effect of contact point-specific deep brain stimulation in Parkinson’s disease: A proof of concept study
title Magnetoencephalography to measure the effect of contact point-specific deep brain stimulation in Parkinson’s disease: A proof of concept study
title_full Magnetoencephalography to measure the effect of contact point-specific deep brain stimulation in Parkinson’s disease: A proof of concept study
title_fullStr Magnetoencephalography to measure the effect of contact point-specific deep brain stimulation in Parkinson’s disease: A proof of concept study
title_full_unstemmed Magnetoencephalography to measure the effect of contact point-specific deep brain stimulation in Parkinson’s disease: A proof of concept study
title_short Magnetoencephalography to measure the effect of contact point-specific deep brain stimulation in Parkinson’s disease: A proof of concept study
title_sort magnetoencephalography to measure the effect of contact point-specific deep brain stimulation in parkinson’s disease: a proof of concept study
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197095/
https://www.ncbi.nlm.nih.gov/pubmed/37187041
http://dx.doi.org/10.1016/j.nicl.2023.103431
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