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A metabolic readout of the urine metabolome of COVID-19 patients
Analysis of urine samples from COVID-19 patients by (1)H NMR reveals important metabolic alterations due to SAR-CoV-2 infection. Previous studies have identified biomarkers in urine that reflect metabolic alterations in COVID-19 patients. We have used (1)H NMR to better define these metabolic altera...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9873393/ https://www.ncbi.nlm.nih.gov/pubmed/36694097 http://dx.doi.org/10.1007/s11306-023-01971-6 |
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author | Marhuenda-Egea, F. C. Narro-Serrano, J. Shalabi-Benavent, M. J. Álamo-Marzo, J. M. Amador-Prous, C. Algado-Rabasa, J. T. Garijo-Saiz, A. M. Marco-Escoto, M. |
author_facet | Marhuenda-Egea, F. C. Narro-Serrano, J. Shalabi-Benavent, M. J. Álamo-Marzo, J. M. Amador-Prous, C. Algado-Rabasa, J. T. Garijo-Saiz, A. M. Marco-Escoto, M. |
author_sort | Marhuenda-Egea, F. C. |
collection | PubMed |
description | Analysis of urine samples from COVID-19 patients by (1)H NMR reveals important metabolic alterations due to SAR-CoV-2 infection. Previous studies have identified biomarkers in urine that reflect metabolic alterations in COVID-19 patients. We have used (1)H NMR to better define these metabolic alterations since this technique allows us to obtain a broad profile of the metabolites present in urine. This technique offers the advantage that sample preparation is very simple and gives us very complete information on the metabolites present. To detect these alterations, we have compared urine samples from COVID-19 patients (n = 35) with healthy people (n = 18). We used unsupervised (Robust PCA) and supervised (PLS-LDA) multivariate analysis methods to evaluate the differences between the two groups: COVID-19 and healthy controls. The differences focus on a group of metabolites related to energy metabolism (glucose, ketone bodies, glycine, creatinine, and citrate) and other processes related to bacterial flora (TMAO and formic acid) and detoxification (hippuric acid). The alterations in the urinary metabolome shown in this work indicate that SARS-CoV-2 causes a metabolic change from a normal situation of glucose consumption towards a gluconeogenic situation and possible insulin resistance. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11306-023-01971-6. |
format | Online Article Text |
id | pubmed-9873393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-98733932023-01-25 A metabolic readout of the urine metabolome of COVID-19 patients Marhuenda-Egea, F. C. Narro-Serrano, J. Shalabi-Benavent, M. J. Álamo-Marzo, J. M. Amador-Prous, C. Algado-Rabasa, J. T. Garijo-Saiz, A. M. Marco-Escoto, M. Metabolomics Original Article Analysis of urine samples from COVID-19 patients by (1)H NMR reveals important metabolic alterations due to SAR-CoV-2 infection. Previous studies have identified biomarkers in urine that reflect metabolic alterations in COVID-19 patients. We have used (1)H NMR to better define these metabolic alterations since this technique allows us to obtain a broad profile of the metabolites present in urine. This technique offers the advantage that sample preparation is very simple and gives us very complete information on the metabolites present. To detect these alterations, we have compared urine samples from COVID-19 patients (n = 35) with healthy people (n = 18). We used unsupervised (Robust PCA) and supervised (PLS-LDA) multivariate analysis methods to evaluate the differences between the two groups: COVID-19 and healthy controls. The differences focus on a group of metabolites related to energy metabolism (glucose, ketone bodies, glycine, creatinine, and citrate) and other processes related to bacterial flora (TMAO and formic acid) and detoxification (hippuric acid). The alterations in the urinary metabolome shown in this work indicate that SARS-CoV-2 causes a metabolic change from a normal situation of glucose consumption towards a gluconeogenic situation and possible insulin resistance. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11306-023-01971-6. Springer US 2023-01-24 2023 /pmc/articles/PMC9873393/ /pubmed/36694097 http://dx.doi.org/10.1007/s11306-023-01971-6 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article Marhuenda-Egea, F. C. Narro-Serrano, J. Shalabi-Benavent, M. J. Álamo-Marzo, J. M. Amador-Prous, C. Algado-Rabasa, J. T. Garijo-Saiz, A. M. Marco-Escoto, M. A metabolic readout of the urine metabolome of COVID-19 patients |
title | A metabolic readout of the urine metabolome of COVID-19 patients |
title_full | A metabolic readout of the urine metabolome of COVID-19 patients |
title_fullStr | A metabolic readout of the urine metabolome of COVID-19 patients |
title_full_unstemmed | A metabolic readout of the urine metabolome of COVID-19 patients |
title_short | A metabolic readout of the urine metabolome of COVID-19 patients |
title_sort | metabolic readout of the urine metabolome of covid-19 patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9873393/ https://www.ncbi.nlm.nih.gov/pubmed/36694097 http://dx.doi.org/10.1007/s11306-023-01971-6 |
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