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Serum IL-6: a candidate biomarker for intracranial pressure elevation following isolated traumatic brain injury
BACKGROUND: Increased intracranial pressure (ICP) is a serious, life-threatening, secondary event following traumatic brain injury (TBI). In many cases, ICP rises in a delayed fashion, reaching a maximal level 48-96 hours after the initial insult. While pressure catheters can be implanted to monitor...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2853529/ https://www.ncbi.nlm.nih.gov/pubmed/20222971 http://dx.doi.org/10.1186/1742-2094-7-19 |
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author | Hergenroeder, Georgene W Moore, Anthony N McCoy, J Philip Samsel, Leigh Ward, Norman H Clifton, Guy L Dash, Pramod K |
author_facet | Hergenroeder, Georgene W Moore, Anthony N McCoy, J Philip Samsel, Leigh Ward, Norman H Clifton, Guy L Dash, Pramod K |
author_sort | Hergenroeder, Georgene W |
collection | PubMed |
description | BACKGROUND: Increased intracranial pressure (ICP) is a serious, life-threatening, secondary event following traumatic brain injury (TBI). In many cases, ICP rises in a delayed fashion, reaching a maximal level 48-96 hours after the initial insult. While pressure catheters can be implanted to monitor ICP, there is no clinically proven method for determining a patient's risk for developing this pathology. METHODS: In the present study, we employed antibody array and Luminex-based screening methods to interrogate the levels of inflammatory cytokines in the serum of healthy volunteers and in severe TBI patients (GCS≤8) with or without incidence of elevated intracranial pressure (ICP). De-identified samples and ELISAs were used to confirm the sensitivity and specificity of IL-6 as a prognostic marker of elevated ICP in both isolated TBI patients, and polytrauma patients with TBI. RESULTS: Consistent with previous reports, we observed sustained increases in IL-6 levels in TBI patients irrespective of their ICP status. However, the group of patients who subsequently experienced ICP ≥ 25 mm Hg had significantly higher IL-6 levels within the first 17 hours of injury as compared to the patients whose ICP remained ≤20 mm Hg. When blinded samples (n = 22) were assessed, a serum IL-6 cut-off of <5 pg/ml correctly identified 100% of all the healthy volunteers, a cut-off of >128 pg/ml correctly identified 85% of isolated TBI patients who subsequently developed elevated ICP, and values between these cut-off values correctly identified 75% of all patients whose ICP remained ≤20 mm Hg throughout the study period. In contrast, the marker had no prognostic value in predicting elevated ICP in polytrauma patients with TBI. When the levels of serum IL-6 were assessed in patients with orthopedic injury (n = 7) in the absence of TBI, a significant increase was found in these patients compared to healthy volunteers, albeit lower than that observed in TBI patients. CONCLUSIONS: Our results suggest that serum IL-6 can be used for the differential diagnosis of elevated ICP in isolated TBI. |
format | Text |
id | pubmed-2853529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28535292010-04-13 Serum IL-6: a candidate biomarker for intracranial pressure elevation following isolated traumatic brain injury Hergenroeder, Georgene W Moore, Anthony N McCoy, J Philip Samsel, Leigh Ward, Norman H Clifton, Guy L Dash, Pramod K J Neuroinflammation Research BACKGROUND: Increased intracranial pressure (ICP) is a serious, life-threatening, secondary event following traumatic brain injury (TBI). In many cases, ICP rises in a delayed fashion, reaching a maximal level 48-96 hours after the initial insult. While pressure catheters can be implanted to monitor ICP, there is no clinically proven method for determining a patient's risk for developing this pathology. METHODS: In the present study, we employed antibody array and Luminex-based screening methods to interrogate the levels of inflammatory cytokines in the serum of healthy volunteers and in severe TBI patients (GCS≤8) with or without incidence of elevated intracranial pressure (ICP). De-identified samples and ELISAs were used to confirm the sensitivity and specificity of IL-6 as a prognostic marker of elevated ICP in both isolated TBI patients, and polytrauma patients with TBI. RESULTS: Consistent with previous reports, we observed sustained increases in IL-6 levels in TBI patients irrespective of their ICP status. However, the group of patients who subsequently experienced ICP ≥ 25 mm Hg had significantly higher IL-6 levels within the first 17 hours of injury as compared to the patients whose ICP remained ≤20 mm Hg. When blinded samples (n = 22) were assessed, a serum IL-6 cut-off of <5 pg/ml correctly identified 100% of all the healthy volunteers, a cut-off of >128 pg/ml correctly identified 85% of isolated TBI patients who subsequently developed elevated ICP, and values between these cut-off values correctly identified 75% of all patients whose ICP remained ≤20 mm Hg throughout the study period. In contrast, the marker had no prognostic value in predicting elevated ICP in polytrauma patients with TBI. When the levels of serum IL-6 were assessed in patients with orthopedic injury (n = 7) in the absence of TBI, a significant increase was found in these patients compared to healthy volunteers, albeit lower than that observed in TBI patients. CONCLUSIONS: Our results suggest that serum IL-6 can be used for the differential diagnosis of elevated ICP in isolated TBI. BioMed Central 2010-03-11 /pmc/articles/PMC2853529/ /pubmed/20222971 http://dx.doi.org/10.1186/1742-2094-7-19 Text en Copyright ©2010 Hergenroeder 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 | Research Hergenroeder, Georgene W Moore, Anthony N McCoy, J Philip Samsel, Leigh Ward, Norman H Clifton, Guy L Dash, Pramod K Serum IL-6: a candidate biomarker for intracranial pressure elevation following isolated traumatic brain injury |
title | Serum IL-6: a candidate biomarker for intracranial pressure elevation following isolated traumatic brain injury |
title_full | Serum IL-6: a candidate biomarker for intracranial pressure elevation following isolated traumatic brain injury |
title_fullStr | Serum IL-6: a candidate biomarker for intracranial pressure elevation following isolated traumatic brain injury |
title_full_unstemmed | Serum IL-6: a candidate biomarker for intracranial pressure elevation following isolated traumatic brain injury |
title_short | Serum IL-6: a candidate biomarker for intracranial pressure elevation following isolated traumatic brain injury |
title_sort | serum il-6: a candidate biomarker for intracranial pressure elevation following isolated traumatic brain injury |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2853529/ https://www.ncbi.nlm.nih.gov/pubmed/20222971 http://dx.doi.org/10.1186/1742-2094-7-19 |
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