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Elevated Serum Levels of Mixed Lineage Kinase Domain-Like Protein Predict Survival of Patients during Intensive Care Unit Treatment
Mixed lineage kinase domain-like (MLKL), a crucial regulator of necroptotic cell death, was shown to play a role in inflammatory diseases. However, its role as a biomarker in critical illness and sepsis is currently unknown. We analyzed serum levels of MLKL in 136 critically ill patients at admissio...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828132/ https://www.ncbi.nlm.nih.gov/pubmed/29606984 http://dx.doi.org/10.1155/2018/1983421 |
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author | Vucur, Mihael Roderburg, Christoph Kaiser, Lukas Schneider, Anne Theres Roy, Sanchari Loosen, Sven Heiko Luedde, Mark Trautwein, Christian Koch, Alexander Tacke, Frank Luedde, Tom |
author_facet | Vucur, Mihael Roderburg, Christoph Kaiser, Lukas Schneider, Anne Theres Roy, Sanchari Loosen, Sven Heiko Luedde, Mark Trautwein, Christian Koch, Alexander Tacke, Frank Luedde, Tom |
author_sort | Vucur, Mihael |
collection | PubMed |
description | Mixed lineage kinase domain-like (MLKL), a crucial regulator of necroptotic cell death, was shown to play a role in inflammatory diseases. However, its role as a biomarker in critical illness and sepsis is currently unknown. We analyzed serum levels of MLKL in 136 critically ill patients at admission to the intensive care unit (ICU) and after three days of ICU treatment. Results were compared with 36 healthy controls and correlated with clinical and laboratory patients' data. MLKL serum levels of critically ill patients at admission to the ICU were similar compared to healthy controls. At ICU admission, MLKL serum concentrations were independent of disease severity, presence of sepsis, and etiology of critical illness. In contrast, median serum levels of MLKL after three days of ICU treatment were significantly lower compared to those at admission to the ICU. While serum levels of MLKL at admission were not predictive for short-term survival during ICU treatment, elevated MLKL concentrations at day three were an independent negative predictor of patients' ICU survival. Thus, elevated MLKL levels after three days of ICU treatment were predictive for patients' mortality, indicating that sustained deregulated cell death is associated with an adverse prognosis in critical illness. |
format | Online Article Text |
id | pubmed-5828132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-58281322018-04-01 Elevated Serum Levels of Mixed Lineage Kinase Domain-Like Protein Predict Survival of Patients during Intensive Care Unit Treatment Vucur, Mihael Roderburg, Christoph Kaiser, Lukas Schneider, Anne Theres Roy, Sanchari Loosen, Sven Heiko Luedde, Mark Trautwein, Christian Koch, Alexander Tacke, Frank Luedde, Tom Dis Markers Research Article Mixed lineage kinase domain-like (MLKL), a crucial regulator of necroptotic cell death, was shown to play a role in inflammatory diseases. However, its role as a biomarker in critical illness and sepsis is currently unknown. We analyzed serum levels of MLKL in 136 critically ill patients at admission to the intensive care unit (ICU) and after three days of ICU treatment. Results were compared with 36 healthy controls and correlated with clinical and laboratory patients' data. MLKL serum levels of critically ill patients at admission to the ICU were similar compared to healthy controls. At ICU admission, MLKL serum concentrations were independent of disease severity, presence of sepsis, and etiology of critical illness. In contrast, median serum levels of MLKL after three days of ICU treatment were significantly lower compared to those at admission to the ICU. While serum levels of MLKL at admission were not predictive for short-term survival during ICU treatment, elevated MLKL concentrations at day three were an independent negative predictor of patients' ICU survival. Thus, elevated MLKL levels after three days of ICU treatment were predictive for patients' mortality, indicating that sustained deregulated cell death is associated with an adverse prognosis in critical illness. Hindawi 2018-02-11 /pmc/articles/PMC5828132/ /pubmed/29606984 http://dx.doi.org/10.1155/2018/1983421 Text en Copyright © 2018 Mihael Vucur et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Vucur, Mihael Roderburg, Christoph Kaiser, Lukas Schneider, Anne Theres Roy, Sanchari Loosen, Sven Heiko Luedde, Mark Trautwein, Christian Koch, Alexander Tacke, Frank Luedde, Tom Elevated Serum Levels of Mixed Lineage Kinase Domain-Like Protein Predict Survival of Patients during Intensive Care Unit Treatment |
title | Elevated Serum Levels of Mixed Lineage Kinase Domain-Like Protein Predict Survival of Patients during Intensive Care Unit Treatment |
title_full | Elevated Serum Levels of Mixed Lineage Kinase Domain-Like Protein Predict Survival of Patients during Intensive Care Unit Treatment |
title_fullStr | Elevated Serum Levels of Mixed Lineage Kinase Domain-Like Protein Predict Survival of Patients during Intensive Care Unit Treatment |
title_full_unstemmed | Elevated Serum Levels of Mixed Lineage Kinase Domain-Like Protein Predict Survival of Patients during Intensive Care Unit Treatment |
title_short | Elevated Serum Levels of Mixed Lineage Kinase Domain-Like Protein Predict Survival of Patients during Intensive Care Unit Treatment |
title_sort | elevated serum levels of mixed lineage kinase domain-like protein predict survival of patients during intensive care unit treatment |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828132/ https://www.ncbi.nlm.nih.gov/pubmed/29606984 http://dx.doi.org/10.1155/2018/1983421 |
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