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Targeting Gut Microbiota As a Novel Strategy for Prevention and Treatment of Hypertension, Atrial Fibrillation and Heart Failure: Current Knowledge and Future Perspectives

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Journal Biomedicines
Date 2022 Aug 26
PMID 36009566
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Abstract

Cardiovascular diseases (CVDs) remain the major public health concern worldwide. Over the last two decades, a considerable amount of literature has been published on gut microbiota (GMB) composition and its metabolites, involved in the pathophysiology of CVDs, including arterial hypertension, atrial fibrillation, and congestive heart failure. Although many types of medicines are available to treat CVD, new therapeutic tools are needed to improve clinical outcomes. A challenge that often arises in the researchers' community is how to manipulate the GMB to manage cardiovascular risk factors. Therapeutic strategies designed to manipulate GMB composition and/or its metabolites include dietary approaches, prebiotics/probiotics supplementation, and fecal microbiota transplantation (FMT). In this review, we have focused on three main cardiovascular pathologies (arterial hypertension, atrial fibrillation and heart failure) due to their shared common pathophysiological pathways and structural changes in myocardium, such as inflammation, hypertrophy, fibrosis, and myocardial remodeling. The main aims of the review are: (1) to summarize current knowledge on the key pathophysiologic links between GMB and CVDs, and (2) discuss the results of the studies on GMB modulation for the prevention and treatment of selected CVDs.

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References
1.
Yang W, Zhang S, Zhu J, Jiang H, Jia D, Ou T . Gut microbe-derived metabolite trimethylamine N-oxide accelerates fibroblast-myofibroblast differentiation and induces cardiac fibrosis. J Mol Cell Cardiol. 2019; 134:119-130. DOI: 10.1016/j.yjmcc.2019.07.004. View

2.
Sun S, Lulla A, Sioda M, Winglee K, Wu M, Jacobs Jr D . Gut Microbiota Composition and Blood Pressure. Hypertension. 2019; 73(5):998-1006. PMC: 6458072. DOI: 10.1161/HYPERTENSIONAHA.118.12109. View

3.
Farnworth E, Mainville I, Desjardins M, GARDNER N, Fliss I, Champagne C . Growth of probiotic bacteria and bifidobacteria in a soy yogurt formulation. Int J Food Microbiol. 2007; 116(1):174-81. DOI: 10.1016/j.ijfoodmicro.2006.12.015. View

4.
Gil-Cruz C, Perez-Shibayama C, De Martin A, Ronchi F, Van der Borght K, Niederer R . Microbiota-derived peptide mimics drive lethal inflammatory cardiomyopathy. Science. 2019; 366(6467):881-886. DOI: 10.1126/science.aav3487. View

5.
Costa C, Sampaio-Maia B, Araujo R, Nascimento D, Ferreira-Gomes J, Pestana M . Gut Microbiome and Organ Fibrosis. Nutrients. 2022; 14(2). PMC: 8781069. DOI: 10.3390/nu14020352. View