Literature DB >> 22197776

A combined score of pro- and anti-inflammatory interleukins improves mortality prediction in severe sepsis.

David Andaluz-Ojeda1, Felipe Bobillo, Verónica Iglesias, Raquel Almansa, Lucía Rico, Francisco Gandía, Salvador Resino, Eduardo Tamayo, Raul Ortiz de Lejarazu, Jesús F Bermejo-Martin.   

Abstract

Identification of patients at increased risk of death is dramatically important in severe sepsis. Cytokines have been widely assessed as potential biomarkers in this disease, but none of the cytokines studied has evidenced a sufficient specificity or sensitivity to be routinely employed in clinical practice. In this pilot study, we profiled 17 immune mediators in the plasma of 29 consecutively recruited patients with severe sepsis or septic shock, during the first 24h following admission to the ICU, by using a Bio-Plex Human Cytokine 17-Plex Panel (Bio-Rad). Patients were 66.1year old in average. Twelve patients of our cohort died during hospitalization at the ICU, eight of them in the first 72h due to multiorganic dysfunction syndrom (MODS). Levels in plasma of three pro-inflammatory mediators (IL-6, IL-8, MCP-1) and of an immunosuppressive one (IL-10) were higher in those patients with fatal outcome. We developed a combined score with those cytokines showing to better predict mortality in our cohort based on the results of Cox regression analysis. This way, IL-6, IL-8 and IL-10 were included in the score. Patients were split into two groups based on the percentile 75 (P75) of the plasma levels of these three interleukins. Those patients showing at least one interleukin value higher than P75 were given the value "1". Those patients showing IL-6, IL-8, IL-10 levels below P75 were given the value "0". Hazard ratios for mortality at day 3 and day 28th obtained with the combined score were 2-3-fold higher than those obtained with the individual interleukins values. In conclusion, we have described a combined cytokine score associated with a worse outcome in patients with sepsis, which may represent a new avenue to be explored for guiding treatment decisions in this disease.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 22197776     DOI: 10.1016/j.cyto.2011.12.002

Source DB:  PubMed          Journal:  Cytokine        ISSN: 1043-4666            Impact factor:   3.861


  61 in total

1.  Clinical relevance of IL-6 gene polymorphism in severely injured patients.

Authors:  Vasilije Jeremić; Tamara Alempijević; Srđan Mijatović; Ana Sijački; Sanja Dragašević; Sonja Pavlović; Biljana Miličić; Slobodan Krstić
Journal:  Bosn J Basic Med Sci       Date:  2014-05       Impact factor: 3.363

2.  Inflammatory mediators of systemic inflammation in neonatal sepsis.

Authors:  V Sugitharini; A Prema; E Berla Thangam
Journal:  Inflamm Res       Date:  2013-09-08       Impact factor: 4.575

3.  A systems biological approach reveals multiple crosstalk mechanism between gram-positive and negative bacterial infections: an insight into core mechanism and unique molecular signatures.

Authors:  R Muthukumar; V Alexandar; Berla Thangam; Shiek S S J Ahmed
Journal:  PLoS One       Date:  2014-02-28       Impact factor: 3.240

4.  Early sepsis biomarkers and their relation to mortality.

Authors:  Andreea Cioara; Madalina Valeanu; Nicolae Todor; Victor Cristea; Mihaela Lupse
Journal:  Rom J Anaesth Intensive Care       Date:  2016-10

5.  Hsp90 inhibitors suppress P53 phosphorylation in LPS - induced endothelial inflammation.

Authors:  Nektarios Barabutis; Mohammad A Uddin; John D Catravas
Journal:  Cytokine       Date:  2018-11-09       Impact factor: 3.861

Review 6.  Lubricin as a Therapeutic and Potential Biomarker in Sepsis.

Authors:  Holly Richendrfer; Gregory D Jay
Journal:  Crit Care Clin       Date:  2019-10-21       Impact factor: 3.598

7.  New approaches to sepsis: molecular diagnostics and biomarkers.

Authors:  Konrad Reinhart; Michael Bauer; Niels C Riedemann; Christiane S Hartog
Journal:  Clin Microbiol Rev       Date:  2012-10       Impact factor: 26.132

8.  Sepsis chronically in MARS: systemic cytokine responses are always mixed regardless of the outcome, magnitude, or phase of sepsis.

Authors:  Marcin F Osuchowski; Florin Craciun; Katrin M Weixelbaumer; Elizabeth R Duffy; Daniel G Remick
Journal:  J Immunol       Date:  2012-09-24       Impact factor: 5.422

9.  Variable neuroendocrine-immune dysfunction in individuals with unfavorable outcome after severe traumatic brain injury.

Authors:  M Santarsieri; R G Kumar; P M Kochanek; S Berga; A K Wagner
Journal:  Brain Behav Immun       Date:  2014-09-16       Impact factor: 7.217

10.  Platelet-monocyte aggregate formation and mortality risk in older patients with severe sepsis and septic shock.

Authors:  Matthew T Rondina; McKenzie Carlisle; Tamra Fraughton; Samuel M Brown; Russell R Miller; Estelle S Harris; Andrew S Weyrich; Guy A Zimmerman; Mark A Supiano; Colin K Grissom
Journal:  J Gerontol A Biol Sci Med Sci       Date:  2014-06-10       Impact factor: 6.053

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