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Urinary metabolomic investigations in vitiligo patients
Urinary metabolomics is a useful non-invasive tool for large-scale screening of disease-related metabolites. However, no comprehensive urinary metabolomic analysis of vitiligo is presently available. To investigate the urine metabolic pattern of vitiligo patients, we conducted a combined cross-secti...
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/PMC7582886/ https://www.ncbi.nlm.nih.gov/pubmed/33093609 http://dx.doi.org/10.1038/s41598-020-75135-0 |
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author | Liu, Wei Liu, Xiao-Yan Qian, Yue-Tong Zhou, Dong-Dong Liu, Jia-Wei Chen, Tian Sun, Wei Ma, Dong-Lai |
author_facet | Liu, Wei Liu, Xiao-Yan Qian, Yue-Tong Zhou, Dong-Dong Liu, Jia-Wei Chen, Tian Sun, Wei Ma, Dong-Lai |
author_sort | Liu, Wei |
collection | PubMed |
description | Urinary metabolomics is a useful non-invasive tool for large-scale screening of disease-related metabolites. However, no comprehensive urinary metabolomic analysis of vitiligo is presently available. To investigate the urine metabolic pattern of vitiligo patients, we conducted a combined cross-sectional and prospective self-control cohort study and an untargeted urinary metabolomic analysis. In the cross-sectional study, 295 vitiligo patients and 192 age‐ and sex‐matched controls were enrolled, and 71 differential metabolites between two groups were identified. Pathway enrichment analysis revealed that drug metabolism-cytochrome P450, biopterin metabolism, vitamin B9 (folate) metabolism, selenoamino acid metabolism, and methionine and cysteine metabolism showed significant enrichment in vitiligo patients compared with the status in healthy controls. In the self-control cohort, 46 active vitiligo patients were recruited to analyse the urinary metabolic signatures after treatment. All of these patients were asked to undertake follow-up visits every 2 months three times after first consulting and the disease stage was evaluated compared with that at the last visit. Folate metabolism, linoleate metabolism, leukotriene metabolism, alkaloid biosynthesis, and tyrosine metabolism were predicted to be involved in vitiligo activity. Our study is the first attempt to reveal urinary metabolic signatures of vitiligo patients and provides new insights into the metabolic mechanisms of vitiligo. |
format | Online Article Text |
id | pubmed-7582886 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75828862020-10-23 Urinary metabolomic investigations in vitiligo patients Liu, Wei Liu, Xiao-Yan Qian, Yue-Tong Zhou, Dong-Dong Liu, Jia-Wei Chen, Tian Sun, Wei Ma, Dong-Lai Sci Rep Article Urinary metabolomics is a useful non-invasive tool for large-scale screening of disease-related metabolites. However, no comprehensive urinary metabolomic analysis of vitiligo is presently available. To investigate the urine metabolic pattern of vitiligo patients, we conducted a combined cross-sectional and prospective self-control cohort study and an untargeted urinary metabolomic analysis. In the cross-sectional study, 295 vitiligo patients and 192 age‐ and sex‐matched controls were enrolled, and 71 differential metabolites between two groups were identified. Pathway enrichment analysis revealed that drug metabolism-cytochrome P450, biopterin metabolism, vitamin B9 (folate) metabolism, selenoamino acid metabolism, and methionine and cysteine metabolism showed significant enrichment in vitiligo patients compared with the status in healthy controls. In the self-control cohort, 46 active vitiligo patients were recruited to analyse the urinary metabolic signatures after treatment. All of these patients were asked to undertake follow-up visits every 2 months three times after first consulting and the disease stage was evaluated compared with that at the last visit. Folate metabolism, linoleate metabolism, leukotriene metabolism, alkaloid biosynthesis, and tyrosine metabolism were predicted to be involved in vitiligo activity. Our study is the first attempt to reveal urinary metabolic signatures of vitiligo patients and provides new insights into the metabolic mechanisms of vitiligo. Nature Publishing Group UK 2020-10-22 /pmc/articles/PMC7582886/ /pubmed/33093609 http://dx.doi.org/10.1038/s41598-020-75135-0 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 Liu, Wei Liu, Xiao-Yan Qian, Yue-Tong Zhou, Dong-Dong Liu, Jia-Wei Chen, Tian Sun, Wei Ma, Dong-Lai Urinary metabolomic investigations in vitiligo patients |
title | Urinary metabolomic investigations in vitiligo patients |
title_full | Urinary metabolomic investigations in vitiligo patients |
title_fullStr | Urinary metabolomic investigations in vitiligo patients |
title_full_unstemmed | Urinary metabolomic investigations in vitiligo patients |
title_short | Urinary metabolomic investigations in vitiligo patients |
title_sort | urinary metabolomic investigations in vitiligo patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582886/ https://www.ncbi.nlm.nih.gov/pubmed/33093609 http://dx.doi.org/10.1038/s41598-020-75135-0 |
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