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Pharmacologic attenuation of cross-modal sensory augmentation within the chronic pain insula
Pain can be elicited through all mammalian sensory pathways yet cross-modal sensory integration, and its relationship to clinical pain, is largely unexplored. Centralized chronic pain conditions such as fibromyalgia are often associated with symptoms of multisensory hypersensitivity. In this study,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988086/ https://www.ncbi.nlm.nih.gov/pubmed/27101425 http://dx.doi.org/10.1097/j.pain.0000000000000593 |
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author | Harte, Steven E. Ichesco, Eric Hampson, Johnson P. Peltier, Scott J. Schmidt-Wilcke, Tobias Clauw, Daniel J. Harris, Richard E. |
author_facet | Harte, Steven E. Ichesco, Eric Hampson, Johnson P. Peltier, Scott J. Schmidt-Wilcke, Tobias Clauw, Daniel J. Harris, Richard E. |
author_sort | Harte, Steven E. |
collection | PubMed |
description | Pain can be elicited through all mammalian sensory pathways yet cross-modal sensory integration, and its relationship to clinical pain, is largely unexplored. Centralized chronic pain conditions such as fibromyalgia are often associated with symptoms of multisensory hypersensitivity. In this study, female patients with fibromyalgia demonstrated cross-modal hypersensitivity to visual and pressure stimuli compared with age- and sex-matched healthy controls. Functional magnetic resonance imaging revealed that insular activity evoked by an aversive level of visual stimulation was associated with the intensity of fibromyalgia pain. Moreover, attenuation of this insular activity by the analgesic pregabalin was accompanied by concomitant reductions in clinical pain. A multivariate classification method using support vector machines (SVM) applied to visual-evoked brain activity distinguished patients with fibromyalgia from healthy controls with 82% accuracy. A separate SVM classification of treatment effects on visual-evoked activity reliably identified when patients were administered pregabalin as compared with placebo. Both SVM analyses identified significant weights within the insular cortex during aversive visual stimulation. These data suggest that abnormal integration of multisensory and pain pathways within the insula may represent a pathophysiological mechanism in some chronic pain conditions and that insular response to aversive visual stimulation may have utility as a marker for analgesic drug development. |
format | Online Article Text |
id | pubmed-4988086 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-49880862016-08-30 Pharmacologic attenuation of cross-modal sensory augmentation within the chronic pain insula Harte, Steven E. Ichesco, Eric Hampson, Johnson P. Peltier, Scott J. Schmidt-Wilcke, Tobias Clauw, Daniel J. Harris, Richard E. Pain Research Paper Pain can be elicited through all mammalian sensory pathways yet cross-modal sensory integration, and its relationship to clinical pain, is largely unexplored. Centralized chronic pain conditions such as fibromyalgia are often associated with symptoms of multisensory hypersensitivity. In this study, female patients with fibromyalgia demonstrated cross-modal hypersensitivity to visual and pressure stimuli compared with age- and sex-matched healthy controls. Functional magnetic resonance imaging revealed that insular activity evoked by an aversive level of visual stimulation was associated with the intensity of fibromyalgia pain. Moreover, attenuation of this insular activity by the analgesic pregabalin was accompanied by concomitant reductions in clinical pain. A multivariate classification method using support vector machines (SVM) applied to visual-evoked brain activity distinguished patients with fibromyalgia from healthy controls with 82% accuracy. A separate SVM classification of treatment effects on visual-evoked activity reliably identified when patients were administered pregabalin as compared with placebo. Both SVM analyses identified significant weights within the insular cortex during aversive visual stimulation. These data suggest that abnormal integration of multisensory and pain pathways within the insula may represent a pathophysiological mechanism in some chronic pain conditions and that insular response to aversive visual stimulation may have utility as a marker for analgesic drug development. Wolters Kluwer 2016-04-19 2016-09 /pmc/articles/PMC4988086/ /pubmed/27101425 http://dx.doi.org/10.1097/j.pain.0000000000000593 Text en © 2016 International Association for the Study of Pain This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially. |
spellingShingle | Research Paper Harte, Steven E. Ichesco, Eric Hampson, Johnson P. Peltier, Scott J. Schmidt-Wilcke, Tobias Clauw, Daniel J. Harris, Richard E. Pharmacologic attenuation of cross-modal sensory augmentation within the chronic pain insula |
title | Pharmacologic attenuation of cross-modal sensory augmentation within the chronic pain insula |
title_full | Pharmacologic attenuation of cross-modal sensory augmentation within the chronic pain insula |
title_fullStr | Pharmacologic attenuation of cross-modal sensory augmentation within the chronic pain insula |
title_full_unstemmed | Pharmacologic attenuation of cross-modal sensory augmentation within the chronic pain insula |
title_short | Pharmacologic attenuation of cross-modal sensory augmentation within the chronic pain insula |
title_sort | pharmacologic attenuation of cross-modal sensory augmentation within the chronic pain insula |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988086/ https://www.ncbi.nlm.nih.gov/pubmed/27101425 http://dx.doi.org/10.1097/j.pain.0000000000000593 |
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