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Metabonomics uncovers a reversible proatherogenic lipid profile during infliximab therapy of inflammatory bowel disease
BACKGROUND: One-third of inflammatory bowel disease (IBD) patients show no response to infliximab (IFX) induction therapy, and approximately half of patients responding become unresponsive over time. Thus, identification of potential treatment response biomarkers are of great clinical significance....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5641999/ https://www.ncbi.nlm.nih.gov/pubmed/29032767 http://dx.doi.org/10.1186/s12916-017-0949-7 |
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author | Bjerrum, Jacob Tveiten Steenholdt, Casper Ainsworth, Mark Nielsen, Ole Haagen Reed, Michelle AC Atkins, Karen Günther, Ulrich Leonhard Hao, Fuhua Wang, Yulan |
author_facet | Bjerrum, Jacob Tveiten Steenholdt, Casper Ainsworth, Mark Nielsen, Ole Haagen Reed, Michelle AC Atkins, Karen Günther, Ulrich Leonhard Hao, Fuhua Wang, Yulan |
author_sort | Bjerrum, Jacob Tveiten |
collection | PubMed |
description | BACKGROUND: One-third of inflammatory bowel disease (IBD) patients show no response to infliximab (IFX) induction therapy, and approximately half of patients responding become unresponsive over time. Thus, identification of potential treatment response biomarkers are of great clinical significance. This study employs spectroscopy-based metabolic profiling of serum from patients with IBD treated with IFX and healthy subjects (1) to substantiate the use of spectroscopy as a semi-invasive diagnostic tool, (2) to identify potential biomarkers of treatment response and (3) to characterise the metabolic changes during management of patients with tumour necrosis factor-α inhibitors. METHODS: Successive serum samples collected during IFX induction treatment (weeks 0, 2, 6 and 14) from 87 IBD patients and 37 controls were analysed by (1)H nuclear magnetic resonance (NMR) spectroscopy. Data were analysed with principal components analysis and orthogonal projection to latent structures discriminant analysis using SIMCA-P+ v12 and MATLAB. RESULTS: Metabolic profiles were significantly different between active ulcerative colitis and controls, active Crohn’s disease and controls, and quiescent Crohn’s disease and controls. Metabolites holding differential power belonged primarily to lipids and phospholipids with proatherogenic characteristics and metabolites in the pyruvate metabolism, suggestive of an intense inflammation-driven energy demand. IBD patients not responding to IFX were identified as a potentially distinct group based on their metabolic profile, although no applicable response biomarkers could be singled out in the current setting. CONCLUSION: (1)H NMR spectroscopy of serum samples is a powerful semi-invasive diagnostic tool in flaring IBD. With its use, we provide unique insights into the metabolic changes taking place during induction treatment with IFX. Of distinct clinical relevance is the identification of a reversible proatherogenic lipid profile in IBD patients with active disease, which partially explains the increased risk of cardiovascular disease associated with IBD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12916-017-0949-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5641999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56419992017-10-18 Metabonomics uncovers a reversible proatherogenic lipid profile during infliximab therapy of inflammatory bowel disease Bjerrum, Jacob Tveiten Steenholdt, Casper Ainsworth, Mark Nielsen, Ole Haagen Reed, Michelle AC Atkins, Karen Günther, Ulrich Leonhard Hao, Fuhua Wang, Yulan BMC Med Research Article BACKGROUND: One-third of inflammatory bowel disease (IBD) patients show no response to infliximab (IFX) induction therapy, and approximately half of patients responding become unresponsive over time. Thus, identification of potential treatment response biomarkers are of great clinical significance. This study employs spectroscopy-based metabolic profiling of serum from patients with IBD treated with IFX and healthy subjects (1) to substantiate the use of spectroscopy as a semi-invasive diagnostic tool, (2) to identify potential biomarkers of treatment response and (3) to characterise the metabolic changes during management of patients with tumour necrosis factor-α inhibitors. METHODS: Successive serum samples collected during IFX induction treatment (weeks 0, 2, 6 and 14) from 87 IBD patients and 37 controls were analysed by (1)H nuclear magnetic resonance (NMR) spectroscopy. Data were analysed with principal components analysis and orthogonal projection to latent structures discriminant analysis using SIMCA-P+ v12 and MATLAB. RESULTS: Metabolic profiles were significantly different between active ulcerative colitis and controls, active Crohn’s disease and controls, and quiescent Crohn’s disease and controls. Metabolites holding differential power belonged primarily to lipids and phospholipids with proatherogenic characteristics and metabolites in the pyruvate metabolism, suggestive of an intense inflammation-driven energy demand. IBD patients not responding to IFX were identified as a potentially distinct group based on their metabolic profile, although no applicable response biomarkers could be singled out in the current setting. CONCLUSION: (1)H NMR spectroscopy of serum samples is a powerful semi-invasive diagnostic tool in flaring IBD. With its use, we provide unique insights into the metabolic changes taking place during induction treatment with IFX. Of distinct clinical relevance is the identification of a reversible proatherogenic lipid profile in IBD patients with active disease, which partially explains the increased risk of cardiovascular disease associated with IBD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12916-017-0949-7) contains supplementary material, which is available to authorized users. BioMed Central 2017-10-16 /pmc/articles/PMC5641999/ /pubmed/29032767 http://dx.doi.org/10.1186/s12916-017-0949-7 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Bjerrum, Jacob Tveiten Steenholdt, Casper Ainsworth, Mark Nielsen, Ole Haagen Reed, Michelle AC Atkins, Karen Günther, Ulrich Leonhard Hao, Fuhua Wang, Yulan Metabonomics uncovers a reversible proatherogenic lipid profile during infliximab therapy of inflammatory bowel disease |
title | Metabonomics uncovers a reversible proatherogenic lipid profile during infliximab therapy of inflammatory bowel disease |
title_full | Metabonomics uncovers a reversible proatherogenic lipid profile during infliximab therapy of inflammatory bowel disease |
title_fullStr | Metabonomics uncovers a reversible proatherogenic lipid profile during infliximab therapy of inflammatory bowel disease |
title_full_unstemmed | Metabonomics uncovers a reversible proatherogenic lipid profile during infliximab therapy of inflammatory bowel disease |
title_short | Metabonomics uncovers a reversible proatherogenic lipid profile during infliximab therapy of inflammatory bowel disease |
title_sort | metabonomics uncovers a reversible proatherogenic lipid profile during infliximab therapy of inflammatory bowel disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5641999/ https://www.ncbi.nlm.nih.gov/pubmed/29032767 http://dx.doi.org/10.1186/s12916-017-0949-7 |
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