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Tracking the neurodegenerative gradient after spinal cord injury
OBJECTIVE: To quantify neurodegenerative changes along the cervical spinal cord rostral to a spinal cord injury (SCI) by means of quantitative MRI (qMRI) and to determine its relationship with clinical impairment. METHODS: Thirty chronic SCI patients (15 tetraplegics and 15 paraplegics) and 23 healt...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058923/ https://www.ncbi.nlm.nih.gov/pubmed/32145681 http://dx.doi.org/10.1016/j.nicl.2020.102221 |
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author | Azzarito, Michela Seif, Maryam Kyathanahally, Sreenath Curt, Armin Freund, Patrick |
author_facet | Azzarito, Michela Seif, Maryam Kyathanahally, Sreenath Curt, Armin Freund, Patrick |
author_sort | Azzarito, Michela |
collection | PubMed |
description | OBJECTIVE: To quantify neurodegenerative changes along the cervical spinal cord rostral to a spinal cord injury (SCI) by means of quantitative MRI (qMRI) and to determine its relationship with clinical impairment. METHODS: Thirty chronic SCI patients (15 tetraplegics and 15 paraplegics) and 23 healthy controls underwent a high-resolution T1-weighted and myelin-sensitive magnetization transfer (MT) MRI. We assessed macro- and microstructural changes along the cervical cord from levels C1 to C4, calculating cross-sectional spinal cord area, its anterior-posterior and left-right width and myelin content (i.e. MT). Regression analysis determined associations between qMRI parameters and clinical impairment. RESULTS: In SCI patients, cord area decreased by 2.67 mm(2) (p = 0.004) and left-right width decreased by 0.35 mm (p = 0.002) per cervical cord level in the caudal direction when compared to the healthy controls. This gradient of neurodegeneration was greater in tetraplegic than paraplegics in the cross-sectional cervical cord area (by 3.28 mm(2), p = 0.011), left-right width (by 0.36 mm, p = 0.03), and mean cord MT (by 0.13%, p = 0.04), but independant of lesion severity (p > 0.05). Higher lesion level was associated with greater magnitudes of neurodegeneration. Greater loss in myelin content in the dorsal columns and spinothalamic tract was associated with worse light touch (p = 0.016) and pin prick score (p = 0.024), respectively. CONCLUSIONS: A gradient of neurodegeneration is evident in the cervical cord remote from a SCI. Tract-specific associations with appropriate clinical outcomes highlight that remote neurodegenerative changes are clinically eloquent. Monitoring the neurodegenerative gradient could be used to track treatment effects of regenerative and neuroprotective agents, both in trials targeting cervical and thoracic SCI patients. |
format | Online Article Text |
id | pubmed-7058923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-70589232020-03-09 Tracking the neurodegenerative gradient after spinal cord injury Azzarito, Michela Seif, Maryam Kyathanahally, Sreenath Curt, Armin Freund, Patrick Neuroimage Clin Regular Article OBJECTIVE: To quantify neurodegenerative changes along the cervical spinal cord rostral to a spinal cord injury (SCI) by means of quantitative MRI (qMRI) and to determine its relationship with clinical impairment. METHODS: Thirty chronic SCI patients (15 tetraplegics and 15 paraplegics) and 23 healthy controls underwent a high-resolution T1-weighted and myelin-sensitive magnetization transfer (MT) MRI. We assessed macro- and microstructural changes along the cervical cord from levels C1 to C4, calculating cross-sectional spinal cord area, its anterior-posterior and left-right width and myelin content (i.e. MT). Regression analysis determined associations between qMRI parameters and clinical impairment. RESULTS: In SCI patients, cord area decreased by 2.67 mm(2) (p = 0.004) and left-right width decreased by 0.35 mm (p = 0.002) per cervical cord level in the caudal direction when compared to the healthy controls. This gradient of neurodegeneration was greater in tetraplegic than paraplegics in the cross-sectional cervical cord area (by 3.28 mm(2), p = 0.011), left-right width (by 0.36 mm, p = 0.03), and mean cord MT (by 0.13%, p = 0.04), but independant of lesion severity (p > 0.05). Higher lesion level was associated with greater magnitudes of neurodegeneration. Greater loss in myelin content in the dorsal columns and spinothalamic tract was associated with worse light touch (p = 0.016) and pin prick score (p = 0.024), respectively. CONCLUSIONS: A gradient of neurodegeneration is evident in the cervical cord remote from a SCI. Tract-specific associations with appropriate clinical outcomes highlight that remote neurodegenerative changes are clinically eloquent. Monitoring the neurodegenerative gradient could be used to track treatment effects of regenerative and neuroprotective agents, both in trials targeting cervical and thoracic SCI patients. Elsevier 2020-02-25 /pmc/articles/PMC7058923/ /pubmed/32145681 http://dx.doi.org/10.1016/j.nicl.2020.102221 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Regular Article Azzarito, Michela Seif, Maryam Kyathanahally, Sreenath Curt, Armin Freund, Patrick Tracking the neurodegenerative gradient after spinal cord injury |
title | Tracking the neurodegenerative gradient after spinal cord injury |
title_full | Tracking the neurodegenerative gradient after spinal cord injury |
title_fullStr | Tracking the neurodegenerative gradient after spinal cord injury |
title_full_unstemmed | Tracking the neurodegenerative gradient after spinal cord injury |
title_short | Tracking the neurodegenerative gradient after spinal cord injury |
title_sort | tracking the neurodegenerative gradient after spinal cord injury |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058923/ https://www.ncbi.nlm.nih.gov/pubmed/32145681 http://dx.doi.org/10.1016/j.nicl.2020.102221 |
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