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The Systemic Inflammatory Response to Clostridium difficile Infection

BACKGROUND: The systemic inflammatory response to Clostridium difficile infection (CDI) is incompletely defined, particularly for patients with severe disease. METHODS: Analysis of 315 blood samples from 78 inpatients with CDI (cases), 100 inpatients with diarrhea without CDI (inpatient controls), a...

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Autores principales: Rao, Krishna, Erb-Downward, John R., Walk, Seth T., Micic, Dejan, Falkowski, Nicole, Santhosh, Kavitha, Mogle, Jill A., Ring, Cathrin, Young, Vincent B., Huffnagle, Gary B., Aronoff, David M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958555/
https://www.ncbi.nlm.nih.gov/pubmed/24643077
http://dx.doi.org/10.1371/journal.pone.0092578
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author Rao, Krishna
Erb-Downward, John R.
Walk, Seth T.
Micic, Dejan
Falkowski, Nicole
Santhosh, Kavitha
Mogle, Jill A.
Ring, Cathrin
Young, Vincent B.
Huffnagle, Gary B.
Aronoff, David M.
author_facet Rao, Krishna
Erb-Downward, John R.
Walk, Seth T.
Micic, Dejan
Falkowski, Nicole
Santhosh, Kavitha
Mogle, Jill A.
Ring, Cathrin
Young, Vincent B.
Huffnagle, Gary B.
Aronoff, David M.
author_sort Rao, Krishna
collection PubMed
description BACKGROUND: The systemic inflammatory response to Clostridium difficile infection (CDI) is incompletely defined, particularly for patients with severe disease. METHODS: Analysis of 315 blood samples from 78 inpatients with CDI (cases), 100 inpatients with diarrhea without CDI (inpatient controls), and 137 asymptomatic outpatient controls without CDI was performed. Serum or plasma was obtained from subjects at the time of CDI testing or shortly thereafter. Severe cases had intensive care unit admission, colectomy, or death due to CDI within 30 days after diagnosis. Thirty different circulating inflammatory mediators were quantified using an antibody-linked bead array. Principal component analysis (PCA), multivariate analysis of variance (MANOVA), and logistic regression were used for analysis. RESULTS: Based on MANOVA, cases had a significantly different inflammatory profile from outpatient controls but not from inpatient controls. In logistic regression, only chemokine (C-C motif) ligand 5 (CCL5) levels were associated with cases vs. inpatient controls. Several mediators were associated with cases vs. outpatient controls, especially hepatocyte growth factor, CCL5, and epithelial growth factor (inversely associated). Eight cases were severe and associated with elevations in IL-8, IL-6, and eotaxin. CONCLUSIONS: A broad systemic inflammatory response occurs during CDI and severe cases appear to differ from non-severe infections.
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spelling pubmed-39585552014-03-24 The Systemic Inflammatory Response to Clostridium difficile Infection Rao, Krishna Erb-Downward, John R. Walk, Seth T. Micic, Dejan Falkowski, Nicole Santhosh, Kavitha Mogle, Jill A. Ring, Cathrin Young, Vincent B. Huffnagle, Gary B. Aronoff, David M. PLoS One Research Article BACKGROUND: The systemic inflammatory response to Clostridium difficile infection (CDI) is incompletely defined, particularly for patients with severe disease. METHODS: Analysis of 315 blood samples from 78 inpatients with CDI (cases), 100 inpatients with diarrhea without CDI (inpatient controls), and 137 asymptomatic outpatient controls without CDI was performed. Serum or plasma was obtained from subjects at the time of CDI testing or shortly thereafter. Severe cases had intensive care unit admission, colectomy, or death due to CDI within 30 days after diagnosis. Thirty different circulating inflammatory mediators were quantified using an antibody-linked bead array. Principal component analysis (PCA), multivariate analysis of variance (MANOVA), and logistic regression were used for analysis. RESULTS: Based on MANOVA, cases had a significantly different inflammatory profile from outpatient controls but not from inpatient controls. In logistic regression, only chemokine (C-C motif) ligand 5 (CCL5) levels were associated with cases vs. inpatient controls. Several mediators were associated with cases vs. outpatient controls, especially hepatocyte growth factor, CCL5, and epithelial growth factor (inversely associated). Eight cases were severe and associated with elevations in IL-8, IL-6, and eotaxin. CONCLUSIONS: A broad systemic inflammatory response occurs during CDI and severe cases appear to differ from non-severe infections. Public Library of Science 2014-03-18 /pmc/articles/PMC3958555/ /pubmed/24643077 http://dx.doi.org/10.1371/journal.pone.0092578 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Rao, Krishna
Erb-Downward, John R.
Walk, Seth T.
Micic, Dejan
Falkowski, Nicole
Santhosh, Kavitha
Mogle, Jill A.
Ring, Cathrin
Young, Vincent B.
Huffnagle, Gary B.
Aronoff, David M.
The Systemic Inflammatory Response to Clostridium difficile Infection
title The Systemic Inflammatory Response to Clostridium difficile Infection
title_full The Systemic Inflammatory Response to Clostridium difficile Infection
title_fullStr The Systemic Inflammatory Response to Clostridium difficile Infection
title_full_unstemmed The Systemic Inflammatory Response to Clostridium difficile Infection
title_short The Systemic Inflammatory Response to Clostridium difficile Infection
title_sort systemic inflammatory response to clostridium difficile infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958555/
https://www.ncbi.nlm.nih.gov/pubmed/24643077
http://dx.doi.org/10.1371/journal.pone.0092578
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