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Gut Microbiome and Plasma Metabolomic Analysis in Patients with Myelodysplastic Syndrome
Myelodysplastic syndrome (MDS) is a heterogeneous group of clonal hematopoietic stem cell disorders. Studies have shown the involvement of an abnormal immune system in MDS pathogenesis. The gut microbiota are known to influence host immunity and metabolism, thereby contributing to the development of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110251/ https://www.ncbi.nlm.nih.gov/pubmed/35585879 http://dx.doi.org/10.1155/2022/1482811 |
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author | Jiang, Huijuan Zhao, Xiaoyu Zang, Mengtong Fu, Rong Shao, Zonghong Liu, Chunyan |
author_facet | Jiang, Huijuan Zhao, Xiaoyu Zang, Mengtong Fu, Rong Shao, Zonghong Liu, Chunyan |
author_sort | Jiang, Huijuan |
collection | PubMed |
description | Myelodysplastic syndrome (MDS) is a heterogeneous group of clonal hematopoietic stem cell disorders. Studies have shown the involvement of an abnormal immune system in MDS pathogenesis. The gut microbiota are known to influence host immunity and metabolism, thereby contributing to the development of hematopoietic diseases. In this study, we performed gut microbiome and plasma metabolomic analyses in patients with MDS and healthy controls. We found that patients with MDS had a different gut microbial composition compared to controls. The gut microbiota in MDS patients showed a continuous evolutionary relationship from the phylum to the species level. At the species level, the abundance of Haemophilus parainfluenzae, Streptococcus luteciae, Clostridium citroniae, and Gemmiger formicilis increased, while that of Prevotella copri decreased in MDS patients compared to controls. Moreover, abundance of bacterial genera correlated with the percentage of lymphocyte subsets in patients with MDS. Metabolomic analysis showed that the concentrations of hypoxanthine and pyroglutamic acid were increased, while that of 3a,7a-dihydroxy-5b-cholestan was decreased in MDS patients compared to controls. In conclusion, gut microbiome and plasma metabolomics are altered in patients with MDS, which may be involved in the immunopathogenesis of the disease. |
format | Online Article Text |
id | pubmed-9110251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-91102512022-05-17 Gut Microbiome and Plasma Metabolomic Analysis in Patients with Myelodysplastic Syndrome Jiang, Huijuan Zhao, Xiaoyu Zang, Mengtong Fu, Rong Shao, Zonghong Liu, Chunyan Oxid Med Cell Longev Research Article Myelodysplastic syndrome (MDS) is a heterogeneous group of clonal hematopoietic stem cell disorders. Studies have shown the involvement of an abnormal immune system in MDS pathogenesis. The gut microbiota are known to influence host immunity and metabolism, thereby contributing to the development of hematopoietic diseases. In this study, we performed gut microbiome and plasma metabolomic analyses in patients with MDS and healthy controls. We found that patients with MDS had a different gut microbial composition compared to controls. The gut microbiota in MDS patients showed a continuous evolutionary relationship from the phylum to the species level. At the species level, the abundance of Haemophilus parainfluenzae, Streptococcus luteciae, Clostridium citroniae, and Gemmiger formicilis increased, while that of Prevotella copri decreased in MDS patients compared to controls. Moreover, abundance of bacterial genera correlated with the percentage of lymphocyte subsets in patients with MDS. Metabolomic analysis showed that the concentrations of hypoxanthine and pyroglutamic acid were increased, while that of 3a,7a-dihydroxy-5b-cholestan was decreased in MDS patients compared to controls. In conclusion, gut microbiome and plasma metabolomics are altered in patients with MDS, which may be involved in the immunopathogenesis of the disease. Hindawi 2022-05-09 /pmc/articles/PMC9110251/ /pubmed/35585879 http://dx.doi.org/10.1155/2022/1482811 Text en Copyright © 2022 Huijuan Jiang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Jiang, Huijuan Zhao, Xiaoyu Zang, Mengtong Fu, Rong Shao, Zonghong Liu, Chunyan Gut Microbiome and Plasma Metabolomic Analysis in Patients with Myelodysplastic Syndrome |
title | Gut Microbiome and Plasma Metabolomic Analysis in Patients with Myelodysplastic Syndrome |
title_full | Gut Microbiome and Plasma Metabolomic Analysis in Patients with Myelodysplastic Syndrome |
title_fullStr | Gut Microbiome and Plasma Metabolomic Analysis in Patients with Myelodysplastic Syndrome |
title_full_unstemmed | Gut Microbiome and Plasma Metabolomic Analysis in Patients with Myelodysplastic Syndrome |
title_short | Gut Microbiome and Plasma Metabolomic Analysis in Patients with Myelodysplastic Syndrome |
title_sort | gut microbiome and plasma metabolomic analysis in patients with myelodysplastic syndrome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110251/ https://www.ncbi.nlm.nih.gov/pubmed/35585879 http://dx.doi.org/10.1155/2022/1482811 |
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