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Specific brain morphometric changes in spinal cord injury with and without neuropathic pain
Why only certain patients develop debilitating pain after spinal chord injury and whether structural brain changes are implicated remain unknown. The aim of this study was to determine if patients with chronic, neuropathic below-level pain have specific cerebral changes compared to those who remain...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055864/ https://www.ncbi.nlm.nih.gov/pubmed/24936434 http://dx.doi.org/10.1016/j.nicl.2014.05.014 |
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author | Mole, Tom B. MacIver, Kate Sluming, Vanessa Ridgway, Gerard R. Nurmikko, Turo J. |
author_facet | Mole, Tom B. MacIver, Kate Sluming, Vanessa Ridgway, Gerard R. Nurmikko, Turo J. |
author_sort | Mole, Tom B. |
collection | PubMed |
description | Why only certain patients develop debilitating pain after spinal chord injury and whether structural brain changes are implicated remain unknown. The aim of this study was to determine if patients with chronic, neuropathic below-level pain have specific cerebral changes compared to those who remain pain-free. Voxel-based morphometry of high resolution, T1-weighted images was performed on three subject groups comprising patients with pain (SCI-P, n = 18), patients without pain (SCI-N, n = 12) and age- and sex-matched controls (n = 18). The SCI-P group was first compared directly with the SCI-N group and then subsequently with controls. Overall, grey and white matter changes dependent on the presence of pain were revealed. Significant changes were found within the somatosensory cortex and also in corticospinal tracts and visual-processing areas. When the SCI-P group was directly compared with the SCI-N group, reduced grey matter volume was found in the deafferented leg area of the somatosensory cortex bilaterally. This region negatively correlated with pain intensity. Relative to controls, grey matter in this paracentral primary sensory cortex was decreased in SCI-P but conversely increased in SCI-N. When compared with controls, discrepant corticospinal tract white matter reductions were found in SCI-P and in SCI-N. In the visual cortex, SCI-N showed increased grey matter, whilst the SCI-N showed reduced white matter. In conclusion, structural changes in SCI are related to the presence and degree of below-level pain and involve but are not limited to the sensorimotor cortices. Pain-related structural plasticity may hold clinical implications for the prevention and management of refractory neuropathic pain. |
format | Online Article Text |
id | pubmed-4055864 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-40558642014-06-16 Specific brain morphometric changes in spinal cord injury with and without neuropathic pain Mole, Tom B. MacIver, Kate Sluming, Vanessa Ridgway, Gerard R. Nurmikko, Turo J. Neuroimage Clin Article Why only certain patients develop debilitating pain after spinal chord injury and whether structural brain changes are implicated remain unknown. The aim of this study was to determine if patients with chronic, neuropathic below-level pain have specific cerebral changes compared to those who remain pain-free. Voxel-based morphometry of high resolution, T1-weighted images was performed on three subject groups comprising patients with pain (SCI-P, n = 18), patients without pain (SCI-N, n = 12) and age- and sex-matched controls (n = 18). The SCI-P group was first compared directly with the SCI-N group and then subsequently with controls. Overall, grey and white matter changes dependent on the presence of pain were revealed. Significant changes were found within the somatosensory cortex and also in corticospinal tracts and visual-processing areas. When the SCI-P group was directly compared with the SCI-N group, reduced grey matter volume was found in the deafferented leg area of the somatosensory cortex bilaterally. This region negatively correlated with pain intensity. Relative to controls, grey matter in this paracentral primary sensory cortex was decreased in SCI-P but conversely increased in SCI-N. When compared with controls, discrepant corticospinal tract white matter reductions were found in SCI-P and in SCI-N. In the visual cortex, SCI-N showed increased grey matter, whilst the SCI-N showed reduced white matter. In conclusion, structural changes in SCI are related to the presence and degree of below-level pain and involve but are not limited to the sensorimotor cortices. Pain-related structural plasticity may hold clinical implications for the prevention and management of refractory neuropathic pain. Elsevier 2014-06-02 /pmc/articles/PMC4055864/ /pubmed/24936434 http://dx.doi.org/10.1016/j.nicl.2014.05.014 Text en © 2014 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Mole, Tom B. MacIver, Kate Sluming, Vanessa Ridgway, Gerard R. Nurmikko, Turo J. Specific brain morphometric changes in spinal cord injury with and without neuropathic pain |
title | Specific brain morphometric changes in spinal cord injury with and without neuropathic pain |
title_full | Specific brain morphometric changes in spinal cord injury with and without neuropathic pain |
title_fullStr | Specific brain morphometric changes in spinal cord injury with and without neuropathic pain |
title_full_unstemmed | Specific brain morphometric changes in spinal cord injury with and without neuropathic pain |
title_short | Specific brain morphometric changes in spinal cord injury with and without neuropathic pain |
title_sort | specific brain morphometric changes in spinal cord injury with and without neuropathic pain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055864/ https://www.ncbi.nlm.nih.gov/pubmed/24936434 http://dx.doi.org/10.1016/j.nicl.2014.05.014 |
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