Prognosis Biomarkers of Severe Sepsis and Septic Shock by 1H NMR Urine Metabolomics in the Intensive Care Unit.

Early diagnosis and patient stratification may improve sepsis outcome by a timely start of the proper specific treatment. We aimed to identify metabolomic biomarkers of sepsis in urine by (1)H-NMR spectroscopy to assess the severity and to predict outcomes. Urine samples were collected from 64 patie...

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Main Authors: Monica Garcia-Simon, Jose M Morales, Vicente Modesto-Alapont, Vannina Gonzalez-Marrachelli, Rosa Vento-Rehues, Angela Jorda-Miñana, Jose Blanquer-Olivas, Daniel Monleon
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0140993
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spelling doaj-ff57c2a9894d4988ae77e5504158f7002021-03-03T19:57:44ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-011011e014099310.1371/journal.pone.0140993Prognosis Biomarkers of Severe Sepsis and Septic Shock by 1H NMR Urine Metabolomics in the Intensive Care Unit.Monica Garcia-SimonJose M MoralesVicente Modesto-AlapontVannina Gonzalez-MarrachelliRosa Vento-RehuesAngela Jorda-MiñanaJose Blanquer-OlivasDaniel MonleonEarly diagnosis and patient stratification may improve sepsis outcome by a timely start of the proper specific treatment. We aimed to identify metabolomic biomarkers of sepsis in urine by (1)H-NMR spectroscopy to assess the severity and to predict outcomes. Urine samples were collected from 64 patients with severe sepsis or septic shock in the ICU for a (1)H NMR spectra acquisition. A supervised analysis was performed on the processed spectra, and a predictive model for prognosis (30-days mortality/survival) of sepsis was constructed using partial least-squares discriminant analysis (PLS-DA). In addition, we compared the prediction power of metabolomics data respect the Sequential Organ Failure Assessment (SOFA) score. Supervised multivariate analysis afforded a good predictive model to distinguish the patient groups and detect specific metabolic patterns. Negative prognosis patients presented higher values of ethanol, glucose and hippurate, and on the contrary, lower levels of methionine, glutamine, arginine and phenylalanine. These metabolites could be part of a composite biopattern of the human metabolic response to sepsis shock and its mortality in ICU patients. The internal cross-validation showed robustness of the metabolic predictive model obtained and a better predictive ability in comparison with SOFA values. Our results indicate that NMR metabolic profiling might be helpful for determining the metabolomic phenotype of worst-prognosis septic patients in an early stage. A predictive model for the evolution of septic patients using these metabolites was able to classify cases with more sensitivity and specificity than the well-established organ dysfunction score SOFA.https://doi.org/10.1371/journal.pone.0140993
collection DOAJ
language English
format Article
sources DOAJ
author Monica Garcia-Simon
Jose M Morales
Vicente Modesto-Alapont
Vannina Gonzalez-Marrachelli
Rosa Vento-Rehues
Angela Jorda-Miñana
Jose Blanquer-Olivas
Daniel Monleon
spellingShingle Monica Garcia-Simon
Jose M Morales
Vicente Modesto-Alapont
Vannina Gonzalez-Marrachelli
Rosa Vento-Rehues
Angela Jorda-Miñana
Jose Blanquer-Olivas
Daniel Monleon
Prognosis Biomarkers of Severe Sepsis and Septic Shock by 1H NMR Urine Metabolomics in the Intensive Care Unit.
PLoS ONE
author_facet Monica Garcia-Simon
Jose M Morales
Vicente Modesto-Alapont
Vannina Gonzalez-Marrachelli
Rosa Vento-Rehues
Angela Jorda-Miñana
Jose Blanquer-Olivas
Daniel Monleon
author_sort Monica Garcia-Simon
title Prognosis Biomarkers of Severe Sepsis and Septic Shock by 1H NMR Urine Metabolomics in the Intensive Care Unit.
title_short Prognosis Biomarkers of Severe Sepsis and Septic Shock by 1H NMR Urine Metabolomics in the Intensive Care Unit.
title_full Prognosis Biomarkers of Severe Sepsis and Septic Shock by 1H NMR Urine Metabolomics in the Intensive Care Unit.
title_fullStr Prognosis Biomarkers of Severe Sepsis and Septic Shock by 1H NMR Urine Metabolomics in the Intensive Care Unit.
title_full_unstemmed Prognosis Biomarkers of Severe Sepsis and Septic Shock by 1H NMR Urine Metabolomics in the Intensive Care Unit.
title_sort prognosis biomarkers of severe sepsis and septic shock by 1h nmr urine metabolomics in the intensive care unit.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Early diagnosis and patient stratification may improve sepsis outcome by a timely start of the proper specific treatment. We aimed to identify metabolomic biomarkers of sepsis in urine by (1)H-NMR spectroscopy to assess the severity and to predict outcomes. Urine samples were collected from 64 patients with severe sepsis or septic shock in the ICU for a (1)H NMR spectra acquisition. A supervised analysis was performed on the processed spectra, and a predictive model for prognosis (30-days mortality/survival) of sepsis was constructed using partial least-squares discriminant analysis (PLS-DA). In addition, we compared the prediction power of metabolomics data respect the Sequential Organ Failure Assessment (SOFA) score. Supervised multivariate analysis afforded a good predictive model to distinguish the patient groups and detect specific metabolic patterns. Negative prognosis patients presented higher values of ethanol, glucose and hippurate, and on the contrary, lower levels of methionine, glutamine, arginine and phenylalanine. These metabolites could be part of a composite biopattern of the human metabolic response to sepsis shock and its mortality in ICU patients. The internal cross-validation showed robustness of the metabolic predictive model obtained and a better predictive ability in comparison with SOFA values. Our results indicate that NMR metabolic profiling might be helpful for determining the metabolomic phenotype of worst-prognosis septic patients in an early stage. A predictive model for the evolution of septic patients using these metabolites was able to classify cases with more sensitivity and specificity than the well-established organ dysfunction score SOFA.
url https://doi.org/10.1371/journal.pone.0140993
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