» Articles » PMID: 28772054

Heart Failure is Associated with Depletion of Core Intestinal Microbiota

Overview
Journal ESC Heart Fail
Date 2017 Aug 4
PMID 28772054
Citations 138
Authors
Affiliations
Soon will be listed here.
Abstract

Aims: In spite of current medical treatment approaches, mortality of chronic heart failure (HF) remains high and novel treatment modalities are thus urgently needed. A recent theory proposes a possible impact of the intestinal microbiome on the incidence and clinical course of heart failure. This study sought to systematically investigate, if there are specific changes of the intestinal microbiome in heart failure patients.

Methods And Results: The intestinal microbiome of 20 patients with heart failure with reduced ejection fraction due to ischemic or dilated cardiomyopathy was investigated by applying high-throughput sequencing of the bacterial 16S rRNA gene. Microbial profiles were compared to those of matched controls in which heart failure was ruled out by clinical assessment and NT-proBNP serum levels (n = 20). According to the Shannon diversity index (which measures the intra-individual alpha-diversity) based on the distribution of operational taxonomic units (OTUs), HF cases showed a nominally significantly lower diversity index compared to controls (P  = 0.01), and testing for genera abundance showed a tendency towards a decreased alpha diversity of HF patients. Beta-diversity measures (inter-individual diversity) revealed a highly significant separation of HF cases and controls, (e.g. P  = 0.004). Assessing the individual abundance of core measurable microbiota (CMM), a significant decrease of Coriobacteriaceae, Erysipelotrichaceae and Ruminococcaceae was observed on the family level. In line with that, Blautia, Collinsella, uncl. Erysipelotrichaceae and uncl. Ruminococcaceae showed a significant decrease in HF cases compared to controls on the genus level.

Conclusions: Heart failure patients showed a significantly decreased diversity of the intestinal microbiome as well as a downregulation of key intestinal bacterial groups. Our data point to an altered intestinal microbiome as a potential player in the pathogenesis and progression of heart failure.

Citing Articles

Role of Gut Microbial Metabolites in Ischemic and Non-Ischemic Heart Failure.

Hatamnejad M, Medzikovic L, Dehghanitafti A, Rahman B, Vadgama A, Eghbali M Int J Mol Sci. 2025; 26(5).

PMID: 40076864 PMC: 11900495. DOI: 10.3390/ijms26052242.


Cardiac energy metabolic disorder and gut microbiota imbalance: a study on the therapeutic potential of Shenfu Injection in rats with heart failure.

Zhao Z, Hu Z, Li L Front Microbiol. 2025; 16:1509548.

PMID: 40071211 PMC: 11895768. DOI: 10.3389/fmicb.2025.1509548.


Oxygenation and intestinal perfusion and its association with perturbations of the early life gut microbiota composition of children with congenital heart disease.

Renk H, Schoppmeier U, Muller J, Kuger V, Neunhoeffer F, Gille C Front Microbiol. 2025; 15:1468842.

PMID: 39881980 PMC: 11775010. DOI: 10.3389/fmicb.2024.1468842.


Association of Fontan Pathophysiology With Plasma Bile Acids.

Shah A, Surendran A, Hassan-Tash P, Turnbull C, Johnston N, Goodlett D JACC Adv. 2025; 4(2):101563.

PMID: 39827765 PMC: 11787425. DOI: 10.1016/j.jacadv.2024.101563.


Gut Microbial Dysbiosis and Implications in Solid Organ Transplantation.

Medina C, Aykut B Biomedicines. 2025; 12(12.

PMID: 39767699 PMC: 11673786. DOI: 10.3390/biomedicines12122792.


References
1.
Nagatomo Y, Tang W . Intersections Between Microbiome and Heart Failure: Revisiting the Gut Hypothesis. J Card Fail. 2015; 21(12):973-80. PMC: 4666782. DOI: 10.1016/j.cardfail.2015.09.017. View

2.
Schloss P, Westcott S, Ryabin T, Hall J, Hartmann M, Hollister E . Introducing mothur: open-source, platform-independent, community-supported software for describing and comparing microbial communities. Appl Environ Microbiol. 2009; 75(23):7537-41. PMC: 2786419. DOI: 10.1128/AEM.01541-09. View

3.
Sokol H, Pigneur B, Watterlot L, Lakhdari O, Bermudez-Humaran L, Gratadoux J . Faecalibacterium prausnitzii is an anti-inflammatory commensal bacterium identified by gut microbiota analysis of Crohn disease patients. Proc Natl Acad Sci U S A. 2008; 105(43):16731-6. PMC: 2575488. DOI: 10.1073/pnas.0804812105. View

4.
Jenq R, Taur Y, Devlin S, Ponce D, Goldberg J, Ahr K . Intestinal Blautia Is Associated with Reduced Death from Graft-versus-Host Disease. Biol Blood Marrow Transplant. 2015; 21(8):1373-83. PMC: 4516127. DOI: 10.1016/j.bbmt.2015.04.016. View

5.
Sandek A, Bjarnason I, Volk H, Crane R, Meddings J, Niebauer J . Studies on bacterial endotoxin and intestinal absorption function in patients with chronic heart failure. Int J Cardiol. 2010; 157(1):80-5. DOI: 10.1016/j.ijcard.2010.12.016. View