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Tissue bridges predict recovery after traumatic and ischemic thoracic spinal cord injury

OBJECTIVE: To investigate the spatiotemporal evolution and predictive properties of intramedullary damage and midsagittal tissue bridges at the epicenter of a thoracic spinal cord injury (SCI) using MRI. METHODS: We retrospectively assessed midsagittal T2-weighted scans from 25 patients with thoraci...

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Autores principales: Pfyffer, Dario, Huber, Eveline, Sutter, Reto, Curt, Armin, Freund, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6815206/
https://www.ncbi.nlm.nih.gov/pubmed/31541012
http://dx.doi.org/10.1212/WNL.0000000000008318
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author Pfyffer, Dario
Huber, Eveline
Sutter, Reto
Curt, Armin
Freund, Patrick
author_facet Pfyffer, Dario
Huber, Eveline
Sutter, Reto
Curt, Armin
Freund, Patrick
author_sort Pfyffer, Dario
collection PubMed
description OBJECTIVE: To investigate the spatiotemporal evolution and predictive properties of intramedullary damage and midsagittal tissue bridges at the epicenter of a thoracic spinal cord injury (SCI) using MRI. METHODS: We retrospectively assessed midsagittal T2-weighted scans from 25 patients with thoracic SCI (14 traumatic, 11 ischemic) at 1 month post-SCI. In 12 patients with SCI, linear mixed-effects models on serial MRI explored temporal trajectories of quantifiable lesion markers (area, length, and width) and tissue bridges. Using partial correlation analysis, we assessed associations between structural lesion characteristics at 1 month post-SCI and recovery at 1 year postinjury, adjusting for baseline clinical status, age, and sex. RESULTS: Lesion area decreased by 5.68 mm(2) (p = 0.005), lesion length by 2.14 mm (p = 0.004), and lesion width by 0.13 mm (p = 0.004) per month. Width of tissue bridges increased by 0.06 mm (p = 0.019) per month, being similar in traumatic and ischemic SCI (p = 0.576). Smaller lesion area, length, width, and wider tissue bridges at 1 month post-SCI predicted better recovery at 1-year follow-up. CONCLUSIONS: Over time, the immediate area of cord damage shrunk while the cystic cavity became demarcated. Adjacent to the cyst, midsagittal tissue bridges became visible. The width of tissue bridges at 1 month post-SCI predicted recovery at 1 year follow-up. Measures of lesion area and tissue bridges early after traumatic and ischemic thoracic SCI therefore allow characterizing the evolution of focal cord damage and are predictive of recovery in thoracic SCI. Thus, lesion extent and tissue bridges hold potential to improve diagnosis and patient stratification in interventional trials.
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spelling pubmed-68152062019-11-20 Tissue bridges predict recovery after traumatic and ischemic thoracic spinal cord injury Pfyffer, Dario Huber, Eveline Sutter, Reto Curt, Armin Freund, Patrick Neurology Article OBJECTIVE: To investigate the spatiotemporal evolution and predictive properties of intramedullary damage and midsagittal tissue bridges at the epicenter of a thoracic spinal cord injury (SCI) using MRI. METHODS: We retrospectively assessed midsagittal T2-weighted scans from 25 patients with thoracic SCI (14 traumatic, 11 ischemic) at 1 month post-SCI. In 12 patients with SCI, linear mixed-effects models on serial MRI explored temporal trajectories of quantifiable lesion markers (area, length, and width) and tissue bridges. Using partial correlation analysis, we assessed associations between structural lesion characteristics at 1 month post-SCI and recovery at 1 year postinjury, adjusting for baseline clinical status, age, and sex. RESULTS: Lesion area decreased by 5.68 mm(2) (p = 0.005), lesion length by 2.14 mm (p = 0.004), and lesion width by 0.13 mm (p = 0.004) per month. Width of tissue bridges increased by 0.06 mm (p = 0.019) per month, being similar in traumatic and ischemic SCI (p = 0.576). Smaller lesion area, length, width, and wider tissue bridges at 1 month post-SCI predicted better recovery at 1-year follow-up. CONCLUSIONS: Over time, the immediate area of cord damage shrunk while the cystic cavity became demarcated. Adjacent to the cyst, midsagittal tissue bridges became visible. The width of tissue bridges at 1 month post-SCI predicted recovery at 1 year follow-up. Measures of lesion area and tissue bridges early after traumatic and ischemic thoracic SCI therefore allow characterizing the evolution of focal cord damage and are predictive of recovery in thoracic SCI. Thus, lesion extent and tissue bridges hold potential to improve diagnosis and patient stratification in interventional trials. Lippincott Williams & Wilkins 2019-10-15 /pmc/articles/PMC6815206/ /pubmed/31541012 http://dx.doi.org/10.1212/WNL.0000000000008318 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Pfyffer, Dario
Huber, Eveline
Sutter, Reto
Curt, Armin
Freund, Patrick
Tissue bridges predict recovery after traumatic and ischemic thoracic spinal cord injury
title Tissue bridges predict recovery after traumatic and ischemic thoracic spinal cord injury
title_full Tissue bridges predict recovery after traumatic and ischemic thoracic spinal cord injury
title_fullStr Tissue bridges predict recovery after traumatic and ischemic thoracic spinal cord injury
title_full_unstemmed Tissue bridges predict recovery after traumatic and ischemic thoracic spinal cord injury
title_short Tissue bridges predict recovery after traumatic and ischemic thoracic spinal cord injury
title_sort tissue bridges predict recovery after traumatic and ischemic thoracic spinal cord injury
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6815206/
https://www.ncbi.nlm.nih.gov/pubmed/31541012
http://dx.doi.org/10.1212/WNL.0000000000008318
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