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Neuroanatomical correlates of poststroke complex regional pain syndrome: a voxel-based lesion symptom-mapping study
Complex regional pain syndrome (CRPS) is a common poststroke complication. However, the neural substrates associated with CRPS remain unclear. We investigated the neural correlates associated with poststroke CRPS using voxel-based lesion‒symptom mapping (VLSM) analysis. Among 145 patients with ische...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219671/ https://www.ncbi.nlm.nih.gov/pubmed/34158602 http://dx.doi.org/10.1038/s41598-021-92564-7 |
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author | Lee, Jae-Ik Kwon, Soon-Woo Lee, Ahry Tae, Woo-suk Pyun, Sung-Bom |
author_facet | Lee, Jae-Ik Kwon, Soon-Woo Lee, Ahry Tae, Woo-suk Pyun, Sung-Bom |
author_sort | Lee, Jae-Ik |
collection | PubMed |
description | Complex regional pain syndrome (CRPS) is a common poststroke complication. However, the neural substrates associated with CRPS remain unclear. We investigated the neural correlates associated with poststroke CRPS using voxel-based lesion‒symptom mapping (VLSM) analysis. Among 145 patients with ischemic stroke, 35 were diagnosed with CRPS and categorized into the poststroke CRPS group, and the remaining 110 into the control group. We compared the clinical characteristics between the groups. VLSM analysis was performed to identify the brain region associated with the development of poststroke CRPS. The clinical findings suggested that the poststroke CRPS group had lower muscle strength; lower scores on Fugl‒Meyer assessment, Manual Function Test, Mini-Mental Status Examination; and higher incidence of absent somatosensory evoked potentials in the median nerve than the control group. The head of the caudate nucleus, putamen, and white matter complexes in the corona radiata were significantly associated with poststroke CRPS development in ischemic stroke patients. These results facilitate an understanding of poststroke CRPS pathophysiology. Monitoring patients with lesions in these structures may aid the prevention and early treatment of poststroke CRPS. |
format | Online Article Text |
id | pubmed-8219671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82196712021-06-24 Neuroanatomical correlates of poststroke complex regional pain syndrome: a voxel-based lesion symptom-mapping study Lee, Jae-Ik Kwon, Soon-Woo Lee, Ahry Tae, Woo-suk Pyun, Sung-Bom Sci Rep Article Complex regional pain syndrome (CRPS) is a common poststroke complication. However, the neural substrates associated with CRPS remain unclear. We investigated the neural correlates associated with poststroke CRPS using voxel-based lesion‒symptom mapping (VLSM) analysis. Among 145 patients with ischemic stroke, 35 were diagnosed with CRPS and categorized into the poststroke CRPS group, and the remaining 110 into the control group. We compared the clinical characteristics between the groups. VLSM analysis was performed to identify the brain region associated with the development of poststroke CRPS. The clinical findings suggested that the poststroke CRPS group had lower muscle strength; lower scores on Fugl‒Meyer assessment, Manual Function Test, Mini-Mental Status Examination; and higher incidence of absent somatosensory evoked potentials in the median nerve than the control group. The head of the caudate nucleus, putamen, and white matter complexes in the corona radiata were significantly associated with poststroke CRPS development in ischemic stroke patients. These results facilitate an understanding of poststroke CRPS pathophysiology. Monitoring patients with lesions in these structures may aid the prevention and early treatment of poststroke CRPS. Nature Publishing Group UK 2021-06-22 /pmc/articles/PMC8219671/ /pubmed/34158602 http://dx.doi.org/10.1038/s41598-021-92564-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lee, Jae-Ik Kwon, Soon-Woo Lee, Ahry Tae, Woo-suk Pyun, Sung-Bom Neuroanatomical correlates of poststroke complex regional pain syndrome: a voxel-based lesion symptom-mapping study |
title | Neuroanatomical correlates of poststroke complex regional pain syndrome: a voxel-based lesion symptom-mapping study |
title_full | Neuroanatomical correlates of poststroke complex regional pain syndrome: a voxel-based lesion symptom-mapping study |
title_fullStr | Neuroanatomical correlates of poststroke complex regional pain syndrome: a voxel-based lesion symptom-mapping study |
title_full_unstemmed | Neuroanatomical correlates of poststroke complex regional pain syndrome: a voxel-based lesion symptom-mapping study |
title_short | Neuroanatomical correlates of poststroke complex regional pain syndrome: a voxel-based lesion symptom-mapping study |
title_sort | neuroanatomical correlates of poststroke complex regional pain syndrome: a voxel-based lesion symptom-mapping study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219671/ https://www.ncbi.nlm.nih.gov/pubmed/34158602 http://dx.doi.org/10.1038/s41598-021-92564-7 |
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