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Metabolomic and proteomic analysis of serum from preterm infants with necrotising entercolitis and late-onset sepsis
BACKGROUND: Necrotising enterocolitis (NEC) and late-onset sepsis (LOS) are the leading causes of death among preterm infants in the developed world. This study aimed to explore the serum proteome and metabolome longitudinally in preterm infants with NEC or LOS, matched to controls. METHODS: Ninetee...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823643/ https://www.ncbi.nlm.nih.gov/pubmed/26571220 http://dx.doi.org/10.1038/pr.2015.235 |
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author | Stewart, Christopher J Nelson, Andrew Treumann, Achim Skeath, Tom Cummings, Stephen P Embleton, Nicholas D Berrington, Janet E |
author_facet | Stewart, Christopher J Nelson, Andrew Treumann, Achim Skeath, Tom Cummings, Stephen P Embleton, Nicholas D Berrington, Janet E |
author_sort | Stewart, Christopher J |
collection | PubMed |
description | BACKGROUND: Necrotising enterocolitis (NEC) and late-onset sepsis (LOS) are the leading causes of death among preterm infants in the developed world. This study aimed to explore the serum proteome and metabolome longitudinally in preterm infants with NEC or LOS, matched to controls. METHODS: Nineteen patients (10 cases, 9 controls) were included. A sample 14 d prior to and following, as well as at disease diagnosis, was included for cases. Controls had serum matched at diagnosis for corresponding case. All samples (n = 39) underwent shotgun proteomic analysis, and 37 samples also underwent metabolomics analysis using ultra performance liquid chromatography–tandem mass spectrometry. RESULTS: The proteomic and metabolomic profiles of serum were comparable between all infants. Eight proteins were associated with NEC and four proteins were associated with LOS. C-reactive protein was increased in all NEC patients at diagnosis. CONCLUSION: No single protein or metabolite was detected in all NEC or LOS cases which was absent from controls; however, several proteins were identified which were associated with disease status. The differing expression of these proteins between diseased infants potentially relates to differing pathophysiology of disease. Thus, it is unlikely a single biomarker exists for NEC and/or LOS. |
format | Online Article Text |
id | pubmed-4823643 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48236432016-04-21 Metabolomic and proteomic analysis of serum from preterm infants with necrotising entercolitis and late-onset sepsis Stewart, Christopher J Nelson, Andrew Treumann, Achim Skeath, Tom Cummings, Stephen P Embleton, Nicholas D Berrington, Janet E Pediatr Res Translational Investigation BACKGROUND: Necrotising enterocolitis (NEC) and late-onset sepsis (LOS) are the leading causes of death among preterm infants in the developed world. This study aimed to explore the serum proteome and metabolome longitudinally in preterm infants with NEC or LOS, matched to controls. METHODS: Nineteen patients (10 cases, 9 controls) were included. A sample 14 d prior to and following, as well as at disease diagnosis, was included for cases. Controls had serum matched at diagnosis for corresponding case. All samples (n = 39) underwent shotgun proteomic analysis, and 37 samples also underwent metabolomics analysis using ultra performance liquid chromatography–tandem mass spectrometry. RESULTS: The proteomic and metabolomic profiles of serum were comparable between all infants. Eight proteins were associated with NEC and four proteins were associated with LOS. C-reactive protein was increased in all NEC patients at diagnosis. CONCLUSION: No single protein or metabolite was detected in all NEC or LOS cases which was absent from controls; however, several proteins were identified which were associated with disease status. The differing expression of these proteins between diseased infants potentially relates to differing pathophysiology of disease. Thus, it is unlikely a single biomarker exists for NEC and/or LOS. Nature Publishing Group 2016-03 2015-12-09 /pmc/articles/PMC4823643/ /pubmed/26571220 http://dx.doi.org/10.1038/pr.2015.235 Text en Copyright © 2016 Official journal of the International Pediatric Research Foundation, Inc. http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Translational Investigation Stewart, Christopher J Nelson, Andrew Treumann, Achim Skeath, Tom Cummings, Stephen P Embleton, Nicholas D Berrington, Janet E Metabolomic and proteomic analysis of serum from preterm infants with necrotising entercolitis and late-onset sepsis |
title | Metabolomic and proteomic analysis of serum from preterm infants with necrotising entercolitis and late-onset sepsis |
title_full | Metabolomic and proteomic analysis of serum from preterm infants with necrotising entercolitis and late-onset sepsis |
title_fullStr | Metabolomic and proteomic analysis of serum from preterm infants with necrotising entercolitis and late-onset sepsis |
title_full_unstemmed | Metabolomic and proteomic analysis of serum from preterm infants with necrotising entercolitis and late-onset sepsis |
title_short | Metabolomic and proteomic analysis of serum from preterm infants with necrotising entercolitis and late-onset sepsis |
title_sort | metabolomic and proteomic analysis of serum from preterm infants with necrotising entercolitis and late-onset sepsis |
topic | Translational Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4823643/ https://www.ncbi.nlm.nih.gov/pubmed/26571220 http://dx.doi.org/10.1038/pr.2015.235 |
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