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Serum Perilipin 2 (PLIN2) Predicts Multiple Organ Dysfunction in Critically Ill Patients
Perilipin 2 (PLIN2) is a lipid droplet protein with various metabolic functions. However, studies investigating PLIN2 in the context of inflammation, especially in systemic and acute inflammation, are lacking. Hence, we assessed the relevance of serum PLIN2 in critically ill patients. We measured se...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8468514/ https://www.ncbi.nlm.nih.gov/pubmed/34572396 http://dx.doi.org/10.3390/biomedicines9091210 |
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author | Kurt, Berkan Buendgens, Lukas Wirtz, Theresa H. Loosen, Sven H. Schulze-Hagen, Maximilian Truhn, Daniel Brozat, Jonathan F. Abu Jhaisha, Samira Hohlstein, Philipp Koek, Ger Weiskirchen, Ralf Trautwein, Christian Tacke, Frank Hamesch, Karim Koch, Alexander |
author_facet | Kurt, Berkan Buendgens, Lukas Wirtz, Theresa H. Loosen, Sven H. Schulze-Hagen, Maximilian Truhn, Daniel Brozat, Jonathan F. Abu Jhaisha, Samira Hohlstein, Philipp Koek, Ger Weiskirchen, Ralf Trautwein, Christian Tacke, Frank Hamesch, Karim Koch, Alexander |
author_sort | Kurt, Berkan |
collection | PubMed |
description | Perilipin 2 (PLIN2) is a lipid droplet protein with various metabolic functions. However, studies investigating PLIN2 in the context of inflammation, especially in systemic and acute inflammation, are lacking. Hence, we assessed the relevance of serum PLIN2 in critically ill patients. We measured serum PLIN2 serum in 259 critically ill patients (166 with sepsis) upon admission to a medical intensive care unit (ICU) compared to 12 healthy controls. A subset of 36 patients underwent computed tomography to quantify body composition. Compared to controls, serum PLIN2 concentrations were elevated in critically ill patients at ICU admission. Interestingly, PLIN2 independently indicated multiple organ dysfunction (MOD), defined as a SOFA score > 9 points, at ICU admission, and was also able to independently predict MOD after 48 h. Moreover, serum PLIN2 levels were associated with severe respiratory failure potentially reflecting a moribund state. However, PLIN2 was neither a predictor of ICU mortality nor did it reflect metabolic dysregulation. Conclusively, the first study assessing serum PLIN2 in critical illness proved that it may assist in risk stratification because it is capable of independently indicating MOD at admission and predicting MOD 48 h after PLIN2 measurement. Further evaluation regarding the underlying mechanisms is warranted. |
format | Online Article Text |
id | pubmed-8468514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84685142021-09-27 Serum Perilipin 2 (PLIN2) Predicts Multiple Organ Dysfunction in Critically Ill Patients Kurt, Berkan Buendgens, Lukas Wirtz, Theresa H. Loosen, Sven H. Schulze-Hagen, Maximilian Truhn, Daniel Brozat, Jonathan F. Abu Jhaisha, Samira Hohlstein, Philipp Koek, Ger Weiskirchen, Ralf Trautwein, Christian Tacke, Frank Hamesch, Karim Koch, Alexander Biomedicines Article Perilipin 2 (PLIN2) is a lipid droplet protein with various metabolic functions. However, studies investigating PLIN2 in the context of inflammation, especially in systemic and acute inflammation, are lacking. Hence, we assessed the relevance of serum PLIN2 in critically ill patients. We measured serum PLIN2 serum in 259 critically ill patients (166 with sepsis) upon admission to a medical intensive care unit (ICU) compared to 12 healthy controls. A subset of 36 patients underwent computed tomography to quantify body composition. Compared to controls, serum PLIN2 concentrations were elevated in critically ill patients at ICU admission. Interestingly, PLIN2 independently indicated multiple organ dysfunction (MOD), defined as a SOFA score > 9 points, at ICU admission, and was also able to independently predict MOD after 48 h. Moreover, serum PLIN2 levels were associated with severe respiratory failure potentially reflecting a moribund state. However, PLIN2 was neither a predictor of ICU mortality nor did it reflect metabolic dysregulation. Conclusively, the first study assessing serum PLIN2 in critical illness proved that it may assist in risk stratification because it is capable of independently indicating MOD at admission and predicting MOD 48 h after PLIN2 measurement. Further evaluation regarding the underlying mechanisms is warranted. MDPI 2021-09-13 /pmc/articles/PMC8468514/ /pubmed/34572396 http://dx.doi.org/10.3390/biomedicines9091210 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kurt, Berkan Buendgens, Lukas Wirtz, Theresa H. Loosen, Sven H. Schulze-Hagen, Maximilian Truhn, Daniel Brozat, Jonathan F. Abu Jhaisha, Samira Hohlstein, Philipp Koek, Ger Weiskirchen, Ralf Trautwein, Christian Tacke, Frank Hamesch, Karim Koch, Alexander Serum Perilipin 2 (PLIN2) Predicts Multiple Organ Dysfunction in Critically Ill Patients |
title | Serum Perilipin 2 (PLIN2) Predicts Multiple Organ Dysfunction in Critically Ill Patients |
title_full | Serum Perilipin 2 (PLIN2) Predicts Multiple Organ Dysfunction in Critically Ill Patients |
title_fullStr | Serum Perilipin 2 (PLIN2) Predicts Multiple Organ Dysfunction in Critically Ill Patients |
title_full_unstemmed | Serum Perilipin 2 (PLIN2) Predicts Multiple Organ Dysfunction in Critically Ill Patients |
title_short | Serum Perilipin 2 (PLIN2) Predicts Multiple Organ Dysfunction in Critically Ill Patients |
title_sort | serum perilipin 2 (plin2) predicts multiple organ dysfunction in critically ill patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8468514/ https://www.ncbi.nlm.nih.gov/pubmed/34572396 http://dx.doi.org/10.3390/biomedicines9091210 |
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