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Exploring blood alterations in chronic kidney disease and haemodialysis using metabolomics
Chronic kidney disease (CKD) is characterized by retention of uremic solutes. Compared to patients with non-dialysis dependent CKD, those requiring haemodialysis (HD) have increased morbidity and mortality. We wished to characterise metabolic patterns in CKD compared to HD patients using metabolomic...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658362/ https://www.ncbi.nlm.nih.gov/pubmed/33177589 http://dx.doi.org/10.1038/s41598-020-76524-1 |
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author | Gagnebin, Yoric Jaques, David A. Rudaz, Serge de Seigneux, Sophie Boccard, Julien Ponte, Belén |
author_facet | Gagnebin, Yoric Jaques, David A. Rudaz, Serge de Seigneux, Sophie Boccard, Julien Ponte, Belén |
author_sort | Gagnebin, Yoric |
collection | PubMed |
description | Chronic kidney disease (CKD) is characterized by retention of uremic solutes. Compared to patients with non-dialysis dependent CKD, those requiring haemodialysis (HD) have increased morbidity and mortality. We wished to characterise metabolic patterns in CKD compared to HD patients using metabolomics. Prevalent non-HD CKD KDIGO stage 3b–4 and stage 5 HD outpatients were screened at a single tertiary hospital. Various liquid chromatography approaches hyphenated with mass spectrometry were used to identify 278 metabolites. Unsupervised and supervised data analyses were conducted to characterize metabolic patterns. 69 patients were included in the CKD group and 35 in the HD group. Unsupervised data analysis showed clear clustering of CKD, pre-dialysis (preHD) and post-dialysis (postHD) patients. Supervised data analysis revealed qualitative as well as quantitative differences in individual metabolites profiles between CKD, preHD and postHD states. An original metabolomics framework could discriminate between CKD stages and highlight HD effect based on 278 identified metabolites. Significant differences in metabolic patterns between CKD and HD patients were found overall as well as for specific metabolites. Those findings could explain clinical discrepancies between patients requiring HD and those with earlier stage of CKD. |
format | Online Article Text |
id | pubmed-7658362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76583622020-11-13 Exploring blood alterations in chronic kidney disease and haemodialysis using metabolomics Gagnebin, Yoric Jaques, David A. Rudaz, Serge de Seigneux, Sophie Boccard, Julien Ponte, Belén Sci Rep Article Chronic kidney disease (CKD) is characterized by retention of uremic solutes. Compared to patients with non-dialysis dependent CKD, those requiring haemodialysis (HD) have increased morbidity and mortality. We wished to characterise metabolic patterns in CKD compared to HD patients using metabolomics. Prevalent non-HD CKD KDIGO stage 3b–4 and stage 5 HD outpatients were screened at a single tertiary hospital. Various liquid chromatography approaches hyphenated with mass spectrometry were used to identify 278 metabolites. Unsupervised and supervised data analyses were conducted to characterize metabolic patterns. 69 patients were included in the CKD group and 35 in the HD group. Unsupervised data analysis showed clear clustering of CKD, pre-dialysis (preHD) and post-dialysis (postHD) patients. Supervised data analysis revealed qualitative as well as quantitative differences in individual metabolites profiles between CKD, preHD and postHD states. An original metabolomics framework could discriminate between CKD stages and highlight HD effect based on 278 identified metabolites. Significant differences in metabolic patterns between CKD and HD patients were found overall as well as for specific metabolites. Those findings could explain clinical discrepancies between patients requiring HD and those with earlier stage of CKD. Nature Publishing Group UK 2020-11-11 /pmc/articles/PMC7658362/ /pubmed/33177589 http://dx.doi.org/10.1038/s41598-020-76524-1 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Gagnebin, Yoric Jaques, David A. Rudaz, Serge de Seigneux, Sophie Boccard, Julien Ponte, Belén Exploring blood alterations in chronic kidney disease and haemodialysis using metabolomics |
title | Exploring blood alterations in chronic kidney disease and haemodialysis using metabolomics |
title_full | Exploring blood alterations in chronic kidney disease and haemodialysis using metabolomics |
title_fullStr | Exploring blood alterations in chronic kidney disease and haemodialysis using metabolomics |
title_full_unstemmed | Exploring blood alterations in chronic kidney disease and haemodialysis using metabolomics |
title_short | Exploring blood alterations in chronic kidney disease and haemodialysis using metabolomics |
title_sort | exploring blood alterations in chronic kidney disease and haemodialysis using metabolomics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658362/ https://www.ncbi.nlm.nih.gov/pubmed/33177589 http://dx.doi.org/10.1038/s41598-020-76524-1 |
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