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miR-142-3p Expression Is Predictive for Severe Traumatic Brain Injury (TBI) in Trauma Patients

Background: Predictive biomarkers in biofluids are the most commonly used diagnostic method, but established markers in trauma diagnostics lack accuracy. This study investigates promising microRNAs (miRNA) released from affected tissue after severe trauma that have predictive values for the effects...

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Autores principales: Schindler, Cora Rebecca, Woschek, Mathias, Vollrath, Jan Tilmann, Kontradowitz, Kerstin, Lustenberger, Thomas, Störmann, Philipp, Marzi, Ingo, Henrich, Dirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432828/
https://www.ncbi.nlm.nih.gov/pubmed/32751105
http://dx.doi.org/10.3390/ijms21155381
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author Schindler, Cora Rebecca
Woschek, Mathias
Vollrath, Jan Tilmann
Kontradowitz, Kerstin
Lustenberger, Thomas
Störmann, Philipp
Marzi, Ingo
Henrich, Dirk
author_facet Schindler, Cora Rebecca
Woschek, Mathias
Vollrath, Jan Tilmann
Kontradowitz, Kerstin
Lustenberger, Thomas
Störmann, Philipp
Marzi, Ingo
Henrich, Dirk
author_sort Schindler, Cora Rebecca
collection PubMed
description Background: Predictive biomarkers in biofluids are the most commonly used diagnostic method, but established markers in trauma diagnostics lack accuracy. This study investigates promising microRNAs (miRNA) released from affected tissue after severe trauma that have predictive values for the effects of the injury. Methods: A retrospective analysis of prospectively collected data and blood samples of n = 33 trauma patients (ISS ≥ 16) is provided. Levels of miR-9-5p, -124-3p, -142-3p, -219a-5p, -338-3p and -423-3p in severely injured patients (PT) without traumatic brain injury (TBI) or with severe TBI (PT + TBI) and patients with isolated TBI (isTBI) were measured within 6 h after trauma. Results: The highest miR-423-3p expression was detected in patients with severe isTBI, followed by patients with PT + TBI, and lowest levels were found in PT patients without TBI (2(−∆∆Ct), p = 0.009). A positive correlation between miR-423-3p level and increasing AIS(head) (p = 0.001) and risk of mortality (RISC II, p = 0.062) in trauma patients (n = 33) was found. ROC analysis of miR-423-3p levels revealed them as statistically significant to predict the severity of brain injury in trauma patients (p = 0.006). miR-124-3p was only found in patients with severe TBI, miR-338-3p was shown in all trauma groups. miR-9-5p, miR-142-3p and miR-219a-5p could not be detected in any of the four groups. Conclusion: miR-423-3p expression is significantly elevated after isolated traumatic brain injury and predictable for severe TBI in the first hours after trauma. miR-423-3p could represent a promising new biomarker to identify severe isolated TBI.
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spelling pubmed-74328282020-08-27 miR-142-3p Expression Is Predictive for Severe Traumatic Brain Injury (TBI) in Trauma Patients Schindler, Cora Rebecca Woschek, Mathias Vollrath, Jan Tilmann Kontradowitz, Kerstin Lustenberger, Thomas Störmann, Philipp Marzi, Ingo Henrich, Dirk Int J Mol Sci Article Background: Predictive biomarkers in biofluids are the most commonly used diagnostic method, but established markers in trauma diagnostics lack accuracy. This study investigates promising microRNAs (miRNA) released from affected tissue after severe trauma that have predictive values for the effects of the injury. Methods: A retrospective analysis of prospectively collected data and blood samples of n = 33 trauma patients (ISS ≥ 16) is provided. Levels of miR-9-5p, -124-3p, -142-3p, -219a-5p, -338-3p and -423-3p in severely injured patients (PT) without traumatic brain injury (TBI) or with severe TBI (PT + TBI) and patients with isolated TBI (isTBI) were measured within 6 h after trauma. Results: The highest miR-423-3p expression was detected in patients with severe isTBI, followed by patients with PT + TBI, and lowest levels were found in PT patients without TBI (2(−∆∆Ct), p = 0.009). A positive correlation between miR-423-3p level and increasing AIS(head) (p = 0.001) and risk of mortality (RISC II, p = 0.062) in trauma patients (n = 33) was found. ROC analysis of miR-423-3p levels revealed them as statistically significant to predict the severity of brain injury in trauma patients (p = 0.006). miR-124-3p was only found in patients with severe TBI, miR-338-3p was shown in all trauma groups. miR-9-5p, miR-142-3p and miR-219a-5p could not be detected in any of the four groups. Conclusion: miR-423-3p expression is significantly elevated after isolated traumatic brain injury and predictable for severe TBI in the first hours after trauma. miR-423-3p could represent a promising new biomarker to identify severe isolated TBI. MDPI 2020-07-29 /pmc/articles/PMC7432828/ /pubmed/32751105 http://dx.doi.org/10.3390/ijms21155381 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Schindler, Cora Rebecca
Woschek, Mathias
Vollrath, Jan Tilmann
Kontradowitz, Kerstin
Lustenberger, Thomas
Störmann, Philipp
Marzi, Ingo
Henrich, Dirk
miR-142-3p Expression Is Predictive for Severe Traumatic Brain Injury (TBI) in Trauma Patients
title miR-142-3p Expression Is Predictive for Severe Traumatic Brain Injury (TBI) in Trauma Patients
title_full miR-142-3p Expression Is Predictive for Severe Traumatic Brain Injury (TBI) in Trauma Patients
title_fullStr miR-142-3p Expression Is Predictive for Severe Traumatic Brain Injury (TBI) in Trauma Patients
title_full_unstemmed miR-142-3p Expression Is Predictive for Severe Traumatic Brain Injury (TBI) in Trauma Patients
title_short miR-142-3p Expression Is Predictive for Severe Traumatic Brain Injury (TBI) in Trauma Patients
title_sort mir-142-3p expression is predictive for severe traumatic brain injury (tbi) in trauma patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432828/
https://www.ncbi.nlm.nih.gov/pubmed/32751105
http://dx.doi.org/10.3390/ijms21155381
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