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Pallido-putaminal connectivity predicts outcomes of deep brain stimulation for cervical dystonia

Cervical dystonia is a non-degenerative movement disorder characterized by dysfunction of both motor and sensory cortico-basal ganglia networks. Deep brain stimulation targeted to the internal pallidum is an established treatment, but its specific mechanisms remain elusive, and response to therapy i...

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Autores principales: Raghu, Ashley L B, Eraifej, John, Sarangmat, Nagaraja, Stein, John, FitzGerald, James J, Payne, Stephen, Aziz, Tipu Z, Green, Alexander L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8719844/
https://www.ncbi.nlm.nih.gov/pubmed/34293093
http://dx.doi.org/10.1093/brain/awab280
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author Raghu, Ashley L B
Eraifej, John
Sarangmat, Nagaraja
Stein, John
FitzGerald, James J
Payne, Stephen
Aziz, Tipu Z
Green, Alexander L
author_facet Raghu, Ashley L B
Eraifej, John
Sarangmat, Nagaraja
Stein, John
FitzGerald, James J
Payne, Stephen
Aziz, Tipu Z
Green, Alexander L
author_sort Raghu, Ashley L B
collection PubMed
description Cervical dystonia is a non-degenerative movement disorder characterized by dysfunction of both motor and sensory cortico-basal ganglia networks. Deep brain stimulation targeted to the internal pallidum is an established treatment, but its specific mechanisms remain elusive, and response to therapy is highly variable. Modulation of key dysfunctional networks via axonal connections is likely important. Fifteen patients underwent preoperative diffusion-MRI acquisitions and then progressed to bilateral deep brain stimulation targeting the posterior internal pallidum. Severity of disease was assessed preoperatively and later at follow-up. Scans were used to generate tractography-derived connectivity estimates between the bilateral regions of stimulation and relevant structures. Connectivity to the putamen correlated with clinical improvement, and a series of cortical connectivity-based putaminal parcellations identified the primary motor putamen as the key node (r = 0.70, P = 0.004). A regression model with this connectivity and electrode coordinates explained 68% of the variance in outcomes (r = 0.83, P = 0.001), with both as significant explanatory variables. We conclude that modulation of the primary motor putamen–posterior internal pallidum limb of the cortico-basal ganglia loop is characteristic of successful deep brain stimulation treatment of cervical dystonia. Preoperative diffusion imaging contains additional information that predicts outcomes, implying utility for patient selection and/or individualized targeting.
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spelling pubmed-87198442022-01-05 Pallido-putaminal connectivity predicts outcomes of deep brain stimulation for cervical dystonia Raghu, Ashley L B Eraifej, John Sarangmat, Nagaraja Stein, John FitzGerald, James J Payne, Stephen Aziz, Tipu Z Green, Alexander L Brain Report Cervical dystonia is a non-degenerative movement disorder characterized by dysfunction of both motor and sensory cortico-basal ganglia networks. Deep brain stimulation targeted to the internal pallidum is an established treatment, but its specific mechanisms remain elusive, and response to therapy is highly variable. Modulation of key dysfunctional networks via axonal connections is likely important. Fifteen patients underwent preoperative diffusion-MRI acquisitions and then progressed to bilateral deep brain stimulation targeting the posterior internal pallidum. Severity of disease was assessed preoperatively and later at follow-up. Scans were used to generate tractography-derived connectivity estimates between the bilateral regions of stimulation and relevant structures. Connectivity to the putamen correlated with clinical improvement, and a series of cortical connectivity-based putaminal parcellations identified the primary motor putamen as the key node (r = 0.70, P = 0.004). A regression model with this connectivity and electrode coordinates explained 68% of the variance in outcomes (r = 0.83, P = 0.001), with both as significant explanatory variables. We conclude that modulation of the primary motor putamen–posterior internal pallidum limb of the cortico-basal ganglia loop is characteristic of successful deep brain stimulation treatment of cervical dystonia. Preoperative diffusion imaging contains additional information that predicts outcomes, implying utility for patient selection and/or individualized targeting. Oxford University Press 2021-07-22 /pmc/articles/PMC8719844/ /pubmed/34293093 http://dx.doi.org/10.1093/brain/awab280 Text en © The Author(s) (2021). Published by Oxford University Press on behalf of the Guarantors of Brain. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Report
Raghu, Ashley L B
Eraifej, John
Sarangmat, Nagaraja
Stein, John
FitzGerald, James J
Payne, Stephen
Aziz, Tipu Z
Green, Alexander L
Pallido-putaminal connectivity predicts outcomes of deep brain stimulation for cervical dystonia
title Pallido-putaminal connectivity predicts outcomes of deep brain stimulation for cervical dystonia
title_full Pallido-putaminal connectivity predicts outcomes of deep brain stimulation for cervical dystonia
title_fullStr Pallido-putaminal connectivity predicts outcomes of deep brain stimulation for cervical dystonia
title_full_unstemmed Pallido-putaminal connectivity predicts outcomes of deep brain stimulation for cervical dystonia
title_short Pallido-putaminal connectivity predicts outcomes of deep brain stimulation for cervical dystonia
title_sort pallido-putaminal connectivity predicts outcomes of deep brain stimulation for cervical dystonia
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8719844/
https://www.ncbi.nlm.nih.gov/pubmed/34293093
http://dx.doi.org/10.1093/brain/awab280
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