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Clusterin Plasma Concentrations Are Decreased in Sepsis and Inversely Correlated with Established Markers of Inflammation
Clusterin is a multifunctional protein that is recognized to mediate cellular stress response associated with organ failure, systemic inflammation, and metabolic alterations. The aim of this study was to determine the value of clusterin as a clinical biomarker in critical ill patients with or withou...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9776480/ https://www.ncbi.nlm.nih.gov/pubmed/36553017 http://dx.doi.org/10.3390/diagnostics12123010 |
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author | Yagmur, Eray Abu Jhaisha, Samira Buendgens, Lukas Sapundzhieva, Nadezhda Brozat, Jonathan F. Hohlstein, Philipp Pollmanns, Maike R. Koek, Ger H. Weiskirchen, Ralf Trautwein, Christian Tacke, Frank Wirtz, Theresa H. Koch, Alexander |
author_facet | Yagmur, Eray Abu Jhaisha, Samira Buendgens, Lukas Sapundzhieva, Nadezhda Brozat, Jonathan F. Hohlstein, Philipp Pollmanns, Maike R. Koek, Ger H. Weiskirchen, Ralf Trautwein, Christian Tacke, Frank Wirtz, Theresa H. Koch, Alexander |
author_sort | Yagmur, Eray |
collection | PubMed |
description | Clusterin is a multifunctional protein that is recognized to mediate cellular stress response associated with organ failure, systemic inflammation, and metabolic alterations. The aim of this study was to determine the value of clusterin as a clinical biomarker in critical ill patients with or without sepsis. We analyzed clusterin plasma concentrations in 200 critically ill patients (133 with sepsis, 67 without sepsis) on admission to the medical intensive care unit (ICU). The results were compared with 66 healthy controls. Clusterin plasma concentration was significantly elevated in critically ill patients compared to healthy subjects. Clusterin levels were significantly higher in non-septic ICU patients than in patients with sepsis. Clusterin correlated inversely with routinely used biomarkers of inflammatory response. Furthermore, clusterin levels were higher in ICU patients with pre-existing obesity and type 2 diabetes. Clusterin was not associated with disease severity, organ failure, or mortality in the ICU. This study highlights significantly elevated clusterin levels in critically ill patients, predominantly in non-sepsis conditions, and associates circulating clusterin to inflammatory and metabolic dysfunctions. |
format | Online Article Text |
id | pubmed-9776480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97764802022-12-23 Clusterin Plasma Concentrations Are Decreased in Sepsis and Inversely Correlated with Established Markers of Inflammation Yagmur, Eray Abu Jhaisha, Samira Buendgens, Lukas Sapundzhieva, Nadezhda Brozat, Jonathan F. Hohlstein, Philipp Pollmanns, Maike R. Koek, Ger H. Weiskirchen, Ralf Trautwein, Christian Tacke, Frank Wirtz, Theresa H. Koch, Alexander Diagnostics (Basel) Article Clusterin is a multifunctional protein that is recognized to mediate cellular stress response associated with organ failure, systemic inflammation, and metabolic alterations. The aim of this study was to determine the value of clusterin as a clinical biomarker in critical ill patients with or without sepsis. We analyzed clusterin plasma concentrations in 200 critically ill patients (133 with sepsis, 67 without sepsis) on admission to the medical intensive care unit (ICU). The results were compared with 66 healthy controls. Clusterin plasma concentration was significantly elevated in critically ill patients compared to healthy subjects. Clusterin levels were significantly higher in non-septic ICU patients than in patients with sepsis. Clusterin correlated inversely with routinely used biomarkers of inflammatory response. Furthermore, clusterin levels were higher in ICU patients with pre-existing obesity and type 2 diabetes. Clusterin was not associated with disease severity, organ failure, or mortality in the ICU. This study highlights significantly elevated clusterin levels in critically ill patients, predominantly in non-sepsis conditions, and associates circulating clusterin to inflammatory and metabolic dysfunctions. MDPI 2022-12-01 /pmc/articles/PMC9776480/ /pubmed/36553017 http://dx.doi.org/10.3390/diagnostics12123010 Text en © 2022 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 Yagmur, Eray Abu Jhaisha, Samira Buendgens, Lukas Sapundzhieva, Nadezhda Brozat, Jonathan F. Hohlstein, Philipp Pollmanns, Maike R. Koek, Ger H. Weiskirchen, Ralf Trautwein, Christian Tacke, Frank Wirtz, Theresa H. Koch, Alexander Clusterin Plasma Concentrations Are Decreased in Sepsis and Inversely Correlated with Established Markers of Inflammation |
title | Clusterin Plasma Concentrations Are Decreased in Sepsis and Inversely Correlated with Established Markers of Inflammation |
title_full | Clusterin Plasma Concentrations Are Decreased in Sepsis and Inversely Correlated with Established Markers of Inflammation |
title_fullStr | Clusterin Plasma Concentrations Are Decreased in Sepsis and Inversely Correlated with Established Markers of Inflammation |
title_full_unstemmed | Clusterin Plasma Concentrations Are Decreased in Sepsis and Inversely Correlated with Established Markers of Inflammation |
title_short | Clusterin Plasma Concentrations Are Decreased in Sepsis and Inversely Correlated with Established Markers of Inflammation |
title_sort | clusterin plasma concentrations are decreased in sepsis and inversely correlated with established markers of inflammation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9776480/ https://www.ncbi.nlm.nih.gov/pubmed/36553017 http://dx.doi.org/10.3390/diagnostics12123010 |
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