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Cystatin D (CST5): An ultra-early inflammatory biomarker of traumatic brain injury
Traumatic brain injury (TBI) is set to become the leading cause of neurological disability across all age groups. Currently, no reliable biomarkers exist to help diagnose the severity of TBI to identify patients who are at risk of developing secondary injuries. Thus, the discovery of reliable biomar...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504020/ https://www.ncbi.nlm.nih.gov/pubmed/28694499 http://dx.doi.org/10.1038/s41598-017-04722-5 |
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author | Hill, Lisa J. Di Pietro, Valentina Hazeldine, Jon Davies, David Toman, Emma Logan, Ann Belli, Antonio |
author_facet | Hill, Lisa J. Di Pietro, Valentina Hazeldine, Jon Davies, David Toman, Emma Logan, Ann Belli, Antonio |
author_sort | Hill, Lisa J. |
collection | PubMed |
description | Traumatic brain injury (TBI) is set to become the leading cause of neurological disability across all age groups. Currently, no reliable biomarkers exist to help diagnose the severity of TBI to identify patients who are at risk of developing secondary injuries. Thus, the discovery of reliable biomarkers for the management of TBI would improve clinical interventions. Inflammatory markers are particularly suited for biomarker discovery as TBI leads to very early alterations in inflammatory proteins. Using the Proseek Multiplex Inflammation assay, we measured in patients that had suffered mild TBI (n = 10) or severe TBI (n = 10) with extra-cranial injury or extracranial injury only (EC) (n = 10), 92 inflammation-associated proteins in serum obtained: <1 hr (within 1-hour), 4–12 hr and 48–72 hr post injury. Changes were compared to healthy volunteers (HV). Our results identified CST5, AXIN1 and TRAIL as novel early biomarkers of TBI. CST5 identified patients with severe TBI from all other cohorts and importantly was able to do so within the first hour of injury. AXIN1 and TRAIL were able to discriminate between TBI and HV at <1 hr. We conclude that CST5, AXIN1 and TRAIL are worthy of further study in the context of a pre-hospital or pitch-side test to detect brain injury. |
format | Online Article Text |
id | pubmed-5504020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55040202017-07-12 Cystatin D (CST5): An ultra-early inflammatory biomarker of traumatic brain injury Hill, Lisa J. Di Pietro, Valentina Hazeldine, Jon Davies, David Toman, Emma Logan, Ann Belli, Antonio Sci Rep Article Traumatic brain injury (TBI) is set to become the leading cause of neurological disability across all age groups. Currently, no reliable biomarkers exist to help diagnose the severity of TBI to identify patients who are at risk of developing secondary injuries. Thus, the discovery of reliable biomarkers for the management of TBI would improve clinical interventions. Inflammatory markers are particularly suited for biomarker discovery as TBI leads to very early alterations in inflammatory proteins. Using the Proseek Multiplex Inflammation assay, we measured in patients that had suffered mild TBI (n = 10) or severe TBI (n = 10) with extra-cranial injury or extracranial injury only (EC) (n = 10), 92 inflammation-associated proteins in serum obtained: <1 hr (within 1-hour), 4–12 hr and 48–72 hr post injury. Changes were compared to healthy volunteers (HV). Our results identified CST5, AXIN1 and TRAIL as novel early biomarkers of TBI. CST5 identified patients with severe TBI from all other cohorts and importantly was able to do so within the first hour of injury. AXIN1 and TRAIL were able to discriminate between TBI and HV at <1 hr. We conclude that CST5, AXIN1 and TRAIL are worthy of further study in the context of a pre-hospital or pitch-side test to detect brain injury. Nature Publishing Group UK 2017-07-10 /pmc/articles/PMC5504020/ /pubmed/28694499 http://dx.doi.org/10.1038/s41598-017-04722-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Hill, Lisa J. Di Pietro, Valentina Hazeldine, Jon Davies, David Toman, Emma Logan, Ann Belli, Antonio Cystatin D (CST5): An ultra-early inflammatory biomarker of traumatic brain injury |
title | Cystatin D (CST5): An ultra-early inflammatory biomarker of traumatic brain injury |
title_full | Cystatin D (CST5): An ultra-early inflammatory biomarker of traumatic brain injury |
title_fullStr | Cystatin D (CST5): An ultra-early inflammatory biomarker of traumatic brain injury |
title_full_unstemmed | Cystatin D (CST5): An ultra-early inflammatory biomarker of traumatic brain injury |
title_short | Cystatin D (CST5): An ultra-early inflammatory biomarker of traumatic brain injury |
title_sort | cystatin d (cst5): an ultra-early inflammatory biomarker of traumatic brain injury |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504020/ https://www.ncbi.nlm.nih.gov/pubmed/28694499 http://dx.doi.org/10.1038/s41598-017-04722-5 |
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