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Dorsal subthalamic deep brain stimulation improves pain in Parkinson's disease
INTRODUCTION: Inconsistent effects of subthalamic deep brain stimulation (STN DBS) on pain, a common non-motor symptom of Parkinson's disease (PD), may be due to variations in active contact location relative to some pain-reducing locus of stimulation. This study models and compares the loci of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469498/ https://www.ncbi.nlm.nih.gov/pubmed/37663307 http://dx.doi.org/10.3389/fpain.2023.1240379 |
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author | Askari, Asra Lam, Jordan L. W. Zhu, Brandon J. Lu, Charles W. Chou, Kelvin L. Wyant, Kara J. Patil, Parag G. |
author_facet | Askari, Asra Lam, Jordan L. W. Zhu, Brandon J. Lu, Charles W. Chou, Kelvin L. Wyant, Kara J. Patil, Parag G. |
author_sort | Askari, Asra |
collection | PubMed |
description | INTRODUCTION: Inconsistent effects of subthalamic deep brain stimulation (STN DBS) on pain, a common non-motor symptom of Parkinson's disease (PD), may be due to variations in active contact location relative to some pain-reducing locus of stimulation. This study models and compares the loci of maximal effect for pain reduction and motor improvement in STN DBS. METHODS: We measured Movement Disorder Society Unified PD Rating Scale (MDS-UPDRS) Part I pain score (item-9), and MDS-UPDRS Part III motor score, preoperatively and 6–12 months after STN DBS. An ordinary least-squares regression model was used to examine active contact location as a predictor of follow-up pain score while controlling for baseline pain, age, dopaminergic medication, and motor improvement. An atlas-independent isotropic electric field model was applied to distinguish sites of maximally effective stimulation for pain and motor improvement. RESULTS: In 74 PD patients, mean pain score significantly improved after STN DBS (p = 0.01). In a regression model, more dorsal active contact location was the only significant predictor of pain improvement (R(2) = 0.17, p = 0.03). The stimulation locus for maximal pain improvement was lateral, anterior, and dorsal to that for maximal motor improvement. CONCLUSION: STN stimulation, dorsal to the site of optimal motor improvement, improves pain. This region contains the zona incerta, which is known to modulate pain in humans, and may explain this observation. |
format | Online Article Text |
id | pubmed-10469498 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104694982023-09-01 Dorsal subthalamic deep brain stimulation improves pain in Parkinson's disease Askari, Asra Lam, Jordan L. W. Zhu, Brandon J. Lu, Charles W. Chou, Kelvin L. Wyant, Kara J. Patil, Parag G. Front Pain Res (Lausanne) Pain Research INTRODUCTION: Inconsistent effects of subthalamic deep brain stimulation (STN DBS) on pain, a common non-motor symptom of Parkinson's disease (PD), may be due to variations in active contact location relative to some pain-reducing locus of stimulation. This study models and compares the loci of maximal effect for pain reduction and motor improvement in STN DBS. METHODS: We measured Movement Disorder Society Unified PD Rating Scale (MDS-UPDRS) Part I pain score (item-9), and MDS-UPDRS Part III motor score, preoperatively and 6–12 months after STN DBS. An ordinary least-squares regression model was used to examine active contact location as a predictor of follow-up pain score while controlling for baseline pain, age, dopaminergic medication, and motor improvement. An atlas-independent isotropic electric field model was applied to distinguish sites of maximally effective stimulation for pain and motor improvement. RESULTS: In 74 PD patients, mean pain score significantly improved after STN DBS (p = 0.01). In a regression model, more dorsal active contact location was the only significant predictor of pain improvement (R(2) = 0.17, p = 0.03). The stimulation locus for maximal pain improvement was lateral, anterior, and dorsal to that for maximal motor improvement. CONCLUSION: STN stimulation, dorsal to the site of optimal motor improvement, improves pain. This region contains the zona incerta, which is known to modulate pain in humans, and may explain this observation. Frontiers Media S.A. 2023-08-16 /pmc/articles/PMC10469498/ /pubmed/37663307 http://dx.doi.org/10.3389/fpain.2023.1240379 Text en © 2023 Askari, Lam, Zhu, Lu, Chou, Wyant and Patil. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pain Research Askari, Asra Lam, Jordan L. W. Zhu, Brandon J. Lu, Charles W. Chou, Kelvin L. Wyant, Kara J. Patil, Parag G. Dorsal subthalamic deep brain stimulation improves pain in Parkinson's disease |
title | Dorsal subthalamic deep brain stimulation improves pain in Parkinson's disease |
title_full | Dorsal subthalamic deep brain stimulation improves pain in Parkinson's disease |
title_fullStr | Dorsal subthalamic deep brain stimulation improves pain in Parkinson's disease |
title_full_unstemmed | Dorsal subthalamic deep brain stimulation improves pain in Parkinson's disease |
title_short | Dorsal subthalamic deep brain stimulation improves pain in Parkinson's disease |
title_sort | dorsal subthalamic deep brain stimulation improves pain in parkinson's disease |
topic | Pain Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469498/ https://www.ncbi.nlm.nih.gov/pubmed/37663307 http://dx.doi.org/10.3389/fpain.2023.1240379 |
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