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Maintained high sustained serum malondialdehyde levels after severe brain trauma injury in non-survivor patients
OBJECTIVE: Higher blood malondialdehyde (biomarker of lipid peroxidation) levels in the first hours of traumatic brain injury (TBI) have been found in patients with a worst prognosis. The objective of this study was to determine whether serum malondialdehyde levels during the first week of severe TB...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892146/ https://www.ncbi.nlm.nih.gov/pubmed/31796118 http://dx.doi.org/10.1186/s13104-019-4828-5 |
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author | Lorente, Leonardo Martín, María M. Abreu-González, Pedro Ramos, Luis Cáceres, Juan J. Argueso, Mónica Solé-Violán, Jordi Jiménez, Alejandro García-Marín, Victor |
author_facet | Lorente, Leonardo Martín, María M. Abreu-González, Pedro Ramos, Luis Cáceres, Juan J. Argueso, Mónica Solé-Violán, Jordi Jiménez, Alejandro García-Marín, Victor |
author_sort | Lorente, Leonardo |
collection | PubMed |
description | OBJECTIVE: Higher blood malondialdehyde (biomarker of lipid peroxidation) levels in the first hours of traumatic brain injury (TBI) have been found in patients with a worst prognosis. The objective of this study was to determine whether serum malondialdehyde levels during the first week of severe TBI could be used as mortality biomarkers. This was a multicenter, prospective and observational study performed in six Spanish Intensive Care Units. We included patients with severe TBI (defined as Glasgow Coma Scale < 9), and with Injury Severity Score in non-cranial aspects < 9. We determined serum malondialdehyde concentrations at days 1, 4 and 8 of TBI. We stablished 30-day mortality as the end-point study. RESULTS: We found that serum malondialdehyde concentrations at days 1 (p < 0.001), 4 (p < 0.001), and 8 (p < 0.001) of TBI were higher in non-survivor (n = 34) than in survivor (n = 90) patients. We found an area under curve of serum malondialdehyde concentrations at days 1, 4, and 8 of TBI to predict 30-day mortality of 77% (p < 0.001), 87% (p < 0.001) and 84% (p < 0.001) respectively. Thus, the new and most relevant findings of our study were serum malondialdehyde levels during the first week of TBI could be used as mortality biomarkers. |
format | Online Article Text |
id | pubmed-6892146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68921462019-12-11 Maintained high sustained serum malondialdehyde levels after severe brain trauma injury in non-survivor patients Lorente, Leonardo Martín, María M. Abreu-González, Pedro Ramos, Luis Cáceres, Juan J. Argueso, Mónica Solé-Violán, Jordi Jiménez, Alejandro García-Marín, Victor BMC Res Notes Research Note OBJECTIVE: Higher blood malondialdehyde (biomarker of lipid peroxidation) levels in the first hours of traumatic brain injury (TBI) have been found in patients with a worst prognosis. The objective of this study was to determine whether serum malondialdehyde levels during the first week of severe TBI could be used as mortality biomarkers. This was a multicenter, prospective and observational study performed in six Spanish Intensive Care Units. We included patients with severe TBI (defined as Glasgow Coma Scale < 9), and with Injury Severity Score in non-cranial aspects < 9. We determined serum malondialdehyde concentrations at days 1, 4 and 8 of TBI. We stablished 30-day mortality as the end-point study. RESULTS: We found that serum malondialdehyde concentrations at days 1 (p < 0.001), 4 (p < 0.001), and 8 (p < 0.001) of TBI were higher in non-survivor (n = 34) than in survivor (n = 90) patients. We found an area under curve of serum malondialdehyde concentrations at days 1, 4, and 8 of TBI to predict 30-day mortality of 77% (p < 0.001), 87% (p < 0.001) and 84% (p < 0.001) respectively. Thus, the new and most relevant findings of our study were serum malondialdehyde levels during the first week of TBI could be used as mortality biomarkers. BioMed Central 2019-12-03 /pmc/articles/PMC6892146/ /pubmed/31796118 http://dx.doi.org/10.1186/s13104-019-4828-5 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Note Lorente, Leonardo Martín, María M. Abreu-González, Pedro Ramos, Luis Cáceres, Juan J. Argueso, Mónica Solé-Violán, Jordi Jiménez, Alejandro García-Marín, Victor Maintained high sustained serum malondialdehyde levels after severe brain trauma injury in non-survivor patients |
title | Maintained high sustained serum malondialdehyde levels after severe brain trauma injury in non-survivor patients |
title_full | Maintained high sustained serum malondialdehyde levels after severe brain trauma injury in non-survivor patients |
title_fullStr | Maintained high sustained serum malondialdehyde levels after severe brain trauma injury in non-survivor patients |
title_full_unstemmed | Maintained high sustained serum malondialdehyde levels after severe brain trauma injury in non-survivor patients |
title_short | Maintained high sustained serum malondialdehyde levels after severe brain trauma injury in non-survivor patients |
title_sort | maintained high sustained serum malondialdehyde levels after severe brain trauma injury in non-survivor patients |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892146/ https://www.ncbi.nlm.nih.gov/pubmed/31796118 http://dx.doi.org/10.1186/s13104-019-4828-5 |
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