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Isolated vertebral fractures give elevated serum protein S-100B levels
BACKGROUND: Serum protein S-100B determinations have been widely proposed in the past as markers of traumatic brain injury and used as a predictor of injury severity and outcome. The purpose of this prospective observational case series was therefore to determine S-100B serum levels in patients with...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586018/ https://www.ncbi.nlm.nih.gov/pubmed/18992158 http://dx.doi.org/10.1186/1757-7241-16-13 |
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author | Benneker, Lorin M Leitner, Christoph Martinolli, Luca Robert, Kretschmer Zimmermann, Heinz Exadaktylos, Aristomenis K |
author_facet | Benneker, Lorin M Leitner, Christoph Martinolli, Luca Robert, Kretschmer Zimmermann, Heinz Exadaktylos, Aristomenis K |
author_sort | Benneker, Lorin M |
collection | PubMed |
description | BACKGROUND: Serum protein S-100B determinations have been widely proposed in the past as markers of traumatic brain injury and used as a predictor of injury severity and outcome. The purpose of this prospective observational case series was therefore to determine S-100B serum levels in patients with isolated injuries to the back. METHODS: Between 1 February and 1 May 2008, serum samples for S-100B analysis were obtained within 1 hour of injury from 285 trauma patients. All patients with a head injury, polytrauma, and intoxicated patients were excluded to select isolated injuries to the spine. 19 patients with isolated injury of the back were included. Serum samples for S-100B analysis and CT spine were obtained within 1 hours of injury. RESULTS: CT scans showed vertebral fractures in 12 of the 19 patients (63%). All patients with fractures had elevated S-100B levels. Amongst the remaining 7 patients without a fracture, only one patient with a severe spinal contusion had an S-100B concentration above the reference limit. The mean S-100B value of the group with fractures was more than 4 times higher than in the group without fractures (0.385 vs 0.087 μg/L, p = 0.0097). CONCLUSION: Our data, although limited due to a very small sample size, suggest that S-100B serum levels might be useful for the diagnosis of acute vertebral body and spinal cord injury with a high negative predictive power. According to the literature, the highest levels of serum S-100B are found when large bones are fractured. If a large prospective study confirms our findings, determining the S-100B level may contribute to more selective use of CT and MRI in spinal trauma. |
format | Text |
id | pubmed-2586018 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-25860182008-11-22 Isolated vertebral fractures give elevated serum protein S-100B levels Benneker, Lorin M Leitner, Christoph Martinolli, Luca Robert, Kretschmer Zimmermann, Heinz Exadaktylos, Aristomenis K Scand J Trauma Resusc Emerg Med Original Research BACKGROUND: Serum protein S-100B determinations have been widely proposed in the past as markers of traumatic brain injury and used as a predictor of injury severity and outcome. The purpose of this prospective observational case series was therefore to determine S-100B serum levels in patients with isolated injuries to the back. METHODS: Between 1 February and 1 May 2008, serum samples for S-100B analysis were obtained within 1 hour of injury from 285 trauma patients. All patients with a head injury, polytrauma, and intoxicated patients were excluded to select isolated injuries to the spine. 19 patients with isolated injury of the back were included. Serum samples for S-100B analysis and CT spine were obtained within 1 hours of injury. RESULTS: CT scans showed vertebral fractures in 12 of the 19 patients (63%). All patients with fractures had elevated S-100B levels. Amongst the remaining 7 patients without a fracture, only one patient with a severe spinal contusion had an S-100B concentration above the reference limit. The mean S-100B value of the group with fractures was more than 4 times higher than in the group without fractures (0.385 vs 0.087 μg/L, p = 0.0097). CONCLUSION: Our data, although limited due to a very small sample size, suggest that S-100B serum levels might be useful for the diagnosis of acute vertebral body and spinal cord injury with a high negative predictive power. According to the literature, the highest levels of serum S-100B are found when large bones are fractured. If a large prospective study confirms our findings, determining the S-100B level may contribute to more selective use of CT and MRI in spinal trauma. BioMed Central 2008-11-07 /pmc/articles/PMC2586018/ /pubmed/18992158 http://dx.doi.org/10.1186/1757-7241-16-13 Text en Copyright © 2008 Benneker et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Benneker, Lorin M Leitner, Christoph Martinolli, Luca Robert, Kretschmer Zimmermann, Heinz Exadaktylos, Aristomenis K Isolated vertebral fractures give elevated serum protein S-100B levels |
title | Isolated vertebral fractures give elevated serum protein S-100B levels |
title_full | Isolated vertebral fractures give elevated serum protein S-100B levels |
title_fullStr | Isolated vertebral fractures give elevated serum protein S-100B levels |
title_full_unstemmed | Isolated vertebral fractures give elevated serum protein S-100B levels |
title_short | Isolated vertebral fractures give elevated serum protein S-100B levels |
title_sort | isolated vertebral fractures give elevated serum protein s-100b levels |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2586018/ https://www.ncbi.nlm.nih.gov/pubmed/18992158 http://dx.doi.org/10.1186/1757-7241-16-13 |
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