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Alterations of the Gut Microbiota in Patients With Severe Chronic Heart Failure

Chronic heart failure (CHF) is the final outcome of almost all forms of cardiovascular diseases, remaining the main cause of mortality worldwide. Accumulating evidence is focused on the roles of gut microbial community in cardiovascular disease, but few studies have unveiled the alterations and furt...

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Autores principales: Sun, Weiju, Du, Debing, Fu, Tongze, Han, Ying, Li, Peng, Ju, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8843083/
https://www.ncbi.nlm.nih.gov/pubmed/35173696
http://dx.doi.org/10.3389/fmicb.2021.813289
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author Sun, Weiju
Du, Debing
Fu, Tongze
Han, Ying
Li, Peng
Ju, Hong
author_facet Sun, Weiju
Du, Debing
Fu, Tongze
Han, Ying
Li, Peng
Ju, Hong
author_sort Sun, Weiju
collection PubMed
description Chronic heart failure (CHF) is the final outcome of almost all forms of cardiovascular diseases, remaining the main cause of mortality worldwide. Accumulating evidence is focused on the roles of gut microbial community in cardiovascular disease, but few studies have unveiled the alterations and further directions of gut microbiota in severe CHF patients. Aimed to investigate this deficiency, fecal samples from 29 CHF patients diagnosed with NYHA Class III-IV and 30 healthy controls were collected and then analyzed using bacterial 16S rRNA gene sequencing. As a result, there were many significant differences between the two groups. Firstly, the phylum Firmicutes was found to be remarkably decreased in severe CHF patients, and the phylum Proteobacteria was the second most abundant phyla in severe CHF patients instead of phylum Bacteroides strangely. Secondly, the α diversity indices such as chao1, PD-whole-tree and Shannon indices were significantly decreased in the severe CHF versus the control group, as well as the notable difference in β-diversity between the two groups. Thirdly, our result revealed a remarkable decrease in the abundance of the short-chain fatty acids (SCFA)-producing bacteria including genera Ruminococcaceae UCG-004, Ruminococcaceae UCG-002, Lachnospiraceae FCS020 group, Dialister and the increased abundance of the genera in Enterococcus and Enterococcaceae with an increased production of lactic acid. Finally, the alternation of the gut microbiota was presumably associated with the function including Cell cycle control, cell division, chromosome partitioning, Amino acid transport and metabolism and Carbohydrate transport and metabolism through SCFA pathway. Our findings provide the direction and theoretical knowledge for the regulation of gut flora in the treatment of severe CHF.
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spelling pubmed-88430832022-02-15 Alterations of the Gut Microbiota in Patients With Severe Chronic Heart Failure Sun, Weiju Du, Debing Fu, Tongze Han, Ying Li, Peng Ju, Hong Front Microbiol Microbiology Chronic heart failure (CHF) is the final outcome of almost all forms of cardiovascular diseases, remaining the main cause of mortality worldwide. Accumulating evidence is focused on the roles of gut microbial community in cardiovascular disease, but few studies have unveiled the alterations and further directions of gut microbiota in severe CHF patients. Aimed to investigate this deficiency, fecal samples from 29 CHF patients diagnosed with NYHA Class III-IV and 30 healthy controls were collected and then analyzed using bacterial 16S rRNA gene sequencing. As a result, there were many significant differences between the two groups. Firstly, the phylum Firmicutes was found to be remarkably decreased in severe CHF patients, and the phylum Proteobacteria was the second most abundant phyla in severe CHF patients instead of phylum Bacteroides strangely. Secondly, the α diversity indices such as chao1, PD-whole-tree and Shannon indices were significantly decreased in the severe CHF versus the control group, as well as the notable difference in β-diversity between the two groups. Thirdly, our result revealed a remarkable decrease in the abundance of the short-chain fatty acids (SCFA)-producing bacteria including genera Ruminococcaceae UCG-004, Ruminococcaceae UCG-002, Lachnospiraceae FCS020 group, Dialister and the increased abundance of the genera in Enterococcus and Enterococcaceae with an increased production of lactic acid. Finally, the alternation of the gut microbiota was presumably associated with the function including Cell cycle control, cell division, chromosome partitioning, Amino acid transport and metabolism and Carbohydrate transport and metabolism through SCFA pathway. Our findings provide the direction and theoretical knowledge for the regulation of gut flora in the treatment of severe CHF. Frontiers Media S.A. 2022-01-31 /pmc/articles/PMC8843083/ /pubmed/35173696 http://dx.doi.org/10.3389/fmicb.2021.813289 Text en Copyright © 2022 Sun, Du, Fu, Han, Li and Ju. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Sun, Weiju
Du, Debing
Fu, Tongze
Han, Ying
Li, Peng
Ju, Hong
Alterations of the Gut Microbiota in Patients With Severe Chronic Heart Failure
title Alterations of the Gut Microbiota in Patients With Severe Chronic Heart Failure
title_full Alterations of the Gut Microbiota in Patients With Severe Chronic Heart Failure
title_fullStr Alterations of the Gut Microbiota in Patients With Severe Chronic Heart Failure
title_full_unstemmed Alterations of the Gut Microbiota in Patients With Severe Chronic Heart Failure
title_short Alterations of the Gut Microbiota in Patients With Severe Chronic Heart Failure
title_sort alterations of the gut microbiota in patients with severe chronic heart failure
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8843083/
https://www.ncbi.nlm.nih.gov/pubmed/35173696
http://dx.doi.org/10.3389/fmicb.2021.813289
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