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Brain Morphological Signatures for Chronic Pain
Chronic pain can be understood not only as an altered functional state, but also as a consequence of neuronal plasticity. Here we use in vivo structural MRI to compare global, local, and architectural changes in gray matter properties in patients suffering from chronic back pain (CBP), complex regio...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3192794/ https://www.ncbi.nlm.nih.gov/pubmed/22022493 http://dx.doi.org/10.1371/journal.pone.0026010 |
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author | Baliki, Marwan N. Schnitzer, Thomas J. Bauer, William R. Apkarian, A. Vania |
author_facet | Baliki, Marwan N. Schnitzer, Thomas J. Bauer, William R. Apkarian, A. Vania |
author_sort | Baliki, Marwan N. |
collection | PubMed |
description | Chronic pain can be understood not only as an altered functional state, but also as a consequence of neuronal plasticity. Here we use in vivo structural MRI to compare global, local, and architectural changes in gray matter properties in patients suffering from chronic back pain (CBP), complex regional pain syndrome (CRPS) and knee osteoarthritis (OA), relative to healthy controls. We find that different chronic pain types exhibit unique anatomical ‘brain signatures’. Only the CBP group showed altered whole-brain gray matter volume, while regional gray matter density was distinct for each group. Voxel-wise comparison of gray matter density showed that the impact on the extent of chronicity of pain was localized to a common set of regions across all conditions. When gray matter density was examined for large regions approximating Brodmann areas, it exhibited unique large-scale distributed networks for each group. We derived a barcode, summarized by a single index of within-subject co-variation of gray matter density, which enabled classification of individual brains to their conditions with high accuracy. This index also enabled calculating time constants and asymptotic amplitudes for an exponential increase in brain re-organization with pain chronicity, and showed that brain reorganization with pain chronicity was 6 times slower and twice as large in CBP in comparison to CRPS. The results show an exuberance of brain anatomical reorganization peculiar to each condition and as such reflecting the unique maladaptive physiology of different types of chronic pain. |
format | Online Article Text |
id | pubmed-3192794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31927942011-10-21 Brain Morphological Signatures for Chronic Pain Baliki, Marwan N. Schnitzer, Thomas J. Bauer, William R. Apkarian, A. Vania PLoS One Research Article Chronic pain can be understood not only as an altered functional state, but also as a consequence of neuronal plasticity. Here we use in vivo structural MRI to compare global, local, and architectural changes in gray matter properties in patients suffering from chronic back pain (CBP), complex regional pain syndrome (CRPS) and knee osteoarthritis (OA), relative to healthy controls. We find that different chronic pain types exhibit unique anatomical ‘brain signatures’. Only the CBP group showed altered whole-brain gray matter volume, while regional gray matter density was distinct for each group. Voxel-wise comparison of gray matter density showed that the impact on the extent of chronicity of pain was localized to a common set of regions across all conditions. When gray matter density was examined for large regions approximating Brodmann areas, it exhibited unique large-scale distributed networks for each group. We derived a barcode, summarized by a single index of within-subject co-variation of gray matter density, which enabled classification of individual brains to their conditions with high accuracy. This index also enabled calculating time constants and asymptotic amplitudes for an exponential increase in brain re-organization with pain chronicity, and showed that brain reorganization with pain chronicity was 6 times slower and twice as large in CBP in comparison to CRPS. The results show an exuberance of brain anatomical reorganization peculiar to each condition and as such reflecting the unique maladaptive physiology of different types of chronic pain. Public Library of Science 2011-10-13 /pmc/articles/PMC3192794/ /pubmed/22022493 http://dx.doi.org/10.1371/journal.pone.0026010 Text en Baliki et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Baliki, Marwan N. Schnitzer, Thomas J. Bauer, William R. Apkarian, A. Vania Brain Morphological Signatures for Chronic Pain |
title | Brain Morphological Signatures for Chronic Pain |
title_full | Brain Morphological Signatures for Chronic Pain |
title_fullStr | Brain Morphological Signatures for Chronic Pain |
title_full_unstemmed | Brain Morphological Signatures for Chronic Pain |
title_short | Brain Morphological Signatures for Chronic Pain |
title_sort | brain morphological signatures for chronic pain |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3192794/ https://www.ncbi.nlm.nih.gov/pubmed/22022493 http://dx.doi.org/10.1371/journal.pone.0026010 |
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