Discovery of novel plasma biomarker ratios to discriminate traumatic brain injury [version 1; peer review: 2 approved, 1 not approved]

Background: Traumatic brain injury (TBI) is a major cause of death and disability. Despite increased awareness, reliable biomarkers are urgently needed to aid in all forms of traumatic brain injury diagnosis and prognosis. Methods: Here, we aim to assess the diagnostic utility of known and novel TBI...

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Main Authors: Michelle Chen, Antoninus Soosaipillai, Douglas D. Fraser, Eleftherios P. Diamandis
Format: Article
Language:English
Published: F1000 Research Ltd 2019-09-01
Series:F1000Research
Online Access:https://f1000research.com/articles/8-1695/v1
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spelling doaj-c151763a8cfa4b83b572b81bcaebb4e52020-11-25T03:02:05ZengF1000 Research LtdF1000Research2046-14022019-09-01810.12688/f1000research.20445.122476Discovery of novel plasma biomarker ratios to discriminate traumatic brain injury [version 1; peer review: 2 approved, 1 not approved]Michelle Chen0Antoninus Soosaipillai1Douglas D. Fraser2Eleftherios P. Diamandis3Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, CanadaDepartment of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Ontario, CanadaDepartment of Pediatrics, Western University, London, Ontario, CanadaDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, CanadaBackground: Traumatic brain injury (TBI) is a major cause of death and disability. Despite increased awareness, reliable biomarkers are urgently needed to aid in all forms of traumatic brain injury diagnosis and prognosis. Methods: Here, we aim to assess the diagnostic utility of known and novel TBI biomarkers in a pilot patient cohort of severe TBI (sTBI) patients and healthy controls. We analyzed concentrations of S100 calcium binding protein B (S100B), neuron specific enolase (NSE), human kallikrein 6 (hK6) and prostaglandin D2 synthase (PGDS) using ELISA immunoassays. Results: Plasma levels of hK6 and PGDS were significantly lower in sTBI compared with controls, while S100B and NSE were significantly higher. Furthermore, we show that ratios of NSE and S100B with hK6 and PGDS may be able to determine the presence of sTBI better than single markers alone. Conclusions: The findings presented here represent a starting point for future validation, where biomarker ratios can be tested in independent TBI cohorts.https://f1000research.com/articles/8-1695/v1
collection DOAJ
language English
format Article
sources DOAJ
author Michelle Chen
Antoninus Soosaipillai
Douglas D. Fraser
Eleftherios P. Diamandis
spellingShingle Michelle Chen
Antoninus Soosaipillai
Douglas D. Fraser
Eleftherios P. Diamandis
Discovery of novel plasma biomarker ratios to discriminate traumatic brain injury [version 1; peer review: 2 approved, 1 not approved]
F1000Research
author_facet Michelle Chen
Antoninus Soosaipillai
Douglas D. Fraser
Eleftherios P. Diamandis
author_sort Michelle Chen
title Discovery of novel plasma biomarker ratios to discriminate traumatic brain injury [version 1; peer review: 2 approved, 1 not approved]
title_short Discovery of novel plasma biomarker ratios to discriminate traumatic brain injury [version 1; peer review: 2 approved, 1 not approved]
title_full Discovery of novel plasma biomarker ratios to discriminate traumatic brain injury [version 1; peer review: 2 approved, 1 not approved]
title_fullStr Discovery of novel plasma biomarker ratios to discriminate traumatic brain injury [version 1; peer review: 2 approved, 1 not approved]
title_full_unstemmed Discovery of novel plasma biomarker ratios to discriminate traumatic brain injury [version 1; peer review: 2 approved, 1 not approved]
title_sort discovery of novel plasma biomarker ratios to discriminate traumatic brain injury [version 1; peer review: 2 approved, 1 not approved]
publisher F1000 Research Ltd
series F1000Research
issn 2046-1402
publishDate 2019-09-01
description Background: Traumatic brain injury (TBI) is a major cause of death and disability. Despite increased awareness, reliable biomarkers are urgently needed to aid in all forms of traumatic brain injury diagnosis and prognosis. Methods: Here, we aim to assess the diagnostic utility of known and novel TBI biomarkers in a pilot patient cohort of severe TBI (sTBI) patients and healthy controls. We analyzed concentrations of S100 calcium binding protein B (S100B), neuron specific enolase (NSE), human kallikrein 6 (hK6) and prostaglandin D2 synthase (PGDS) using ELISA immunoassays. Results: Plasma levels of hK6 and PGDS were significantly lower in sTBI compared with controls, while S100B and NSE were significantly higher. Furthermore, we show that ratios of NSE and S100B with hK6 and PGDS may be able to determine the presence of sTBI better than single markers alone. Conclusions: The findings presented here represent a starting point for future validation, where biomarker ratios can be tested in independent TBI cohorts.
url https://f1000research.com/articles/8-1695/v1
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