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Quantitative LC–MS study of compounds found predictive of COVID-19 severity and outcome

INTRODUCTION: Since the beginning of the SARS-CoV-2 pandemic in December 2019 multiple metabolomics studies have proposed predictive biomarkers of infection severity and outcome. Whilst some trends have emerged, the findings remain intangible and uninformative when it comes to new patients. OBJECTIV...

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Autores principales: Roberts, Ivayla, Wright Muelas, Marina, Taylor, Joseph M., Davison, Andrew S., Winder, Catherine L., Goodacre, Royston, Kell, Douglas B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584727/
https://www.ncbi.nlm.nih.gov/pubmed/37853293
http://dx.doi.org/10.1007/s11306-023-02048-0
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author Roberts, Ivayla
Wright Muelas, Marina
Taylor, Joseph M.
Davison, Andrew S.
Winder, Catherine L.
Goodacre, Royston
Kell, Douglas B.
author_facet Roberts, Ivayla
Wright Muelas, Marina
Taylor, Joseph M.
Davison, Andrew S.
Winder, Catherine L.
Goodacre, Royston
Kell, Douglas B.
author_sort Roberts, Ivayla
collection PubMed
description INTRODUCTION: Since the beginning of the SARS-CoV-2 pandemic in December 2019 multiple metabolomics studies have proposed predictive biomarkers of infection severity and outcome. Whilst some trends have emerged, the findings remain intangible and uninformative when it comes to new patients. OBJECTIVES: In this study, we accurately quantitate a subset of compounds in patient serum that were found predictive of severity and outcome. METHODS: A targeted LC–MS method was used in 46 control and 95 acute COVID-19 patient samples to quantitate the selected metabolites. These compounds included tryptophan and its degradation products kynurenine and kynurenic acid (reflective of immune response), butyrylcarnitine and its isomer (reflective of energy metabolism) and finally 3′,4′-didehydro-3′-deoxycytidine, a deoxycytidine analogue, (reflective of host viral defence response). We subsequently examine changes in those markers by disease severity and outcome relative to those of control patients’ levels. RESULTS & CONCLUSION: Finally, we demonstrate the added value of the kynurenic acid/tryptophan ratio for severity and outcome prediction and highlight the viral detection potential of ddhC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11306-023-02048-0.
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spelling pubmed-105847272023-10-20 Quantitative LC–MS study of compounds found predictive of COVID-19 severity and outcome Roberts, Ivayla Wright Muelas, Marina Taylor, Joseph M. Davison, Andrew S. Winder, Catherine L. Goodacre, Royston Kell, Douglas B. Metabolomics Original Article INTRODUCTION: Since the beginning of the SARS-CoV-2 pandemic in December 2019 multiple metabolomics studies have proposed predictive biomarkers of infection severity and outcome. Whilst some trends have emerged, the findings remain intangible and uninformative when it comes to new patients. OBJECTIVES: In this study, we accurately quantitate a subset of compounds in patient serum that were found predictive of severity and outcome. METHODS: A targeted LC–MS method was used in 46 control and 95 acute COVID-19 patient samples to quantitate the selected metabolites. These compounds included tryptophan and its degradation products kynurenine and kynurenic acid (reflective of immune response), butyrylcarnitine and its isomer (reflective of energy metabolism) and finally 3′,4′-didehydro-3′-deoxycytidine, a deoxycytidine analogue, (reflective of host viral defence response). We subsequently examine changes in those markers by disease severity and outcome relative to those of control patients’ levels. RESULTS & CONCLUSION: Finally, we demonstrate the added value of the kynurenic acid/tryptophan ratio for severity and outcome prediction and highlight the viral detection potential of ddhC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11306-023-02048-0. Springer US 2023-10-18 2023 /pmc/articles/PMC10584727/ /pubmed/37853293 http://dx.doi.org/10.1007/s11306-023-02048-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Roberts, Ivayla
Wright Muelas, Marina
Taylor, Joseph M.
Davison, Andrew S.
Winder, Catherine L.
Goodacre, Royston
Kell, Douglas B.
Quantitative LC–MS study of compounds found predictive of COVID-19 severity and outcome
title Quantitative LC–MS study of compounds found predictive of COVID-19 severity and outcome
title_full Quantitative LC–MS study of compounds found predictive of COVID-19 severity and outcome
title_fullStr Quantitative LC–MS study of compounds found predictive of COVID-19 severity and outcome
title_full_unstemmed Quantitative LC–MS study of compounds found predictive of COVID-19 severity and outcome
title_short Quantitative LC–MS study of compounds found predictive of COVID-19 severity and outcome
title_sort quantitative lc–ms study of compounds found predictive of covid-19 severity and outcome
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10584727/
https://www.ncbi.nlm.nih.gov/pubmed/37853293
http://dx.doi.org/10.1007/s11306-023-02048-0
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