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Nogo-A Is a Potential Prognostic Marker for Spinal Cord Injury

OBJECTIVE: Spinal cord injury (SCI) has become prevalent worldwide in recent years, and its prognosis is poor and the pathological mechanism has not been fully elucidated. Nogo-A is one of the isoforms of the neurite outgrowth inhibitory protein reticulon 4. The purpose of this study was to determin...

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Autores principales: Shi, Haojun, Xie, Liangyu, Xu, Wenchang, Cao, Shengnan, Chen, Yuanzhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095389/
https://www.ncbi.nlm.nih.gov/pubmed/35571610
http://dx.doi.org/10.1155/2022/2141854
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author Shi, Haojun
Xie, Liangyu
Xu, Wenchang
Cao, Shengnan
Chen, Yuanzhen
author_facet Shi, Haojun
Xie, Liangyu
Xu, Wenchang
Cao, Shengnan
Chen, Yuanzhen
author_sort Shi, Haojun
collection PubMed
description OBJECTIVE: Spinal cord injury (SCI) has become prevalent worldwide in recent years, and its prognosis is poor and the pathological mechanism has not been fully elucidated. Nogo-A is one of the isoforms of the neurite outgrowth inhibitory protein reticulon 4. The purpose of this study was to determine whether Nogo-A could be used as a marker for predicting the prognosis of SCI. METHODS: We screened eligible SCI patients and controls based on inclusion and exclusion criteria. We also collected baseline clinical information and peripheral venous blood of the enrolled population. Participants' baseline serum Nogo-A levels were measured by enzyme-linked immunosorbent assay (ELISA). The American Spinal Injury Association (ASIA) scale was used to evaluate the prognosis of SCI patients after 3 months. RESULTS: Baseline clinical information (age; gender; smoking; drinking; SBP, systolic blood pressure; DBP, diastolic blood pressure; fasting blood glucose; WBC, white blood cells; CRP, C-reactive protein) of SCI patients and controls were not statistically significant academic differences (p > 0.05). The baseline serum Nogo-A levels of SCI patients and controls were 192.7 ± 13.9 ng/ml and 263.1 ± 22.4 ng/ml, respectively, and there was a statistically significant difference between the two groups (p < 0.05). We divided SCI patients into 4 groups according to their baseline serum Nogo-A quartile levels and analyzed their relationship with ASIA scores. The trend test results showed that with the increase of Nogo-A level, the ASIA sensation score and ASIA motor score were significantly decreased (p < 0.001). Multivariate regression analysis showed that serum Nogo-A levels remained a potential cause affecting the prognosis of SCI after adjusting for confounding factors in multiple models. CONCLUSIONS: Serum Nogo-A levels were significantly elevated in SCI patients. Moreover, elevated Nogo-A levels often indicate poor prognosis and can be used as a marker to predict the prognosis of SCI.
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spelling pubmed-90953892022-05-12 Nogo-A Is a Potential Prognostic Marker for Spinal Cord Injury Shi, Haojun Xie, Liangyu Xu, Wenchang Cao, Shengnan Chen, Yuanzhen Dis Markers Research Article OBJECTIVE: Spinal cord injury (SCI) has become prevalent worldwide in recent years, and its prognosis is poor and the pathological mechanism has not been fully elucidated. Nogo-A is one of the isoforms of the neurite outgrowth inhibitory protein reticulon 4. The purpose of this study was to determine whether Nogo-A could be used as a marker for predicting the prognosis of SCI. METHODS: We screened eligible SCI patients and controls based on inclusion and exclusion criteria. We also collected baseline clinical information and peripheral venous blood of the enrolled population. Participants' baseline serum Nogo-A levels were measured by enzyme-linked immunosorbent assay (ELISA). The American Spinal Injury Association (ASIA) scale was used to evaluate the prognosis of SCI patients after 3 months. RESULTS: Baseline clinical information (age; gender; smoking; drinking; SBP, systolic blood pressure; DBP, diastolic blood pressure; fasting blood glucose; WBC, white blood cells; CRP, C-reactive protein) of SCI patients and controls were not statistically significant academic differences (p > 0.05). The baseline serum Nogo-A levels of SCI patients and controls were 192.7 ± 13.9 ng/ml and 263.1 ± 22.4 ng/ml, respectively, and there was a statistically significant difference between the two groups (p < 0.05). We divided SCI patients into 4 groups according to their baseline serum Nogo-A quartile levels and analyzed their relationship with ASIA scores. The trend test results showed that with the increase of Nogo-A level, the ASIA sensation score and ASIA motor score were significantly decreased (p < 0.001). Multivariate regression analysis showed that serum Nogo-A levels remained a potential cause affecting the prognosis of SCI after adjusting for confounding factors in multiple models. CONCLUSIONS: Serum Nogo-A levels were significantly elevated in SCI patients. Moreover, elevated Nogo-A levels often indicate poor prognosis and can be used as a marker to predict the prognosis of SCI. Hindawi 2022-05-04 /pmc/articles/PMC9095389/ /pubmed/35571610 http://dx.doi.org/10.1155/2022/2141854 Text en Copyright © 2022 Haojun Shi et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Shi, Haojun
Xie, Liangyu
Xu, Wenchang
Cao, Shengnan
Chen, Yuanzhen
Nogo-A Is a Potential Prognostic Marker for Spinal Cord Injury
title Nogo-A Is a Potential Prognostic Marker for Spinal Cord Injury
title_full Nogo-A Is a Potential Prognostic Marker for Spinal Cord Injury
title_fullStr Nogo-A Is a Potential Prognostic Marker for Spinal Cord Injury
title_full_unstemmed Nogo-A Is a Potential Prognostic Marker for Spinal Cord Injury
title_short Nogo-A Is a Potential Prognostic Marker for Spinal Cord Injury
title_sort nogo-a is a potential prognostic marker for spinal cord injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095389/
https://www.ncbi.nlm.nih.gov/pubmed/35571610
http://dx.doi.org/10.1155/2022/2141854
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