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Published on: July 31, 2019
Interplay Between Gut Microbiota and Amino Acid Metabolism in Heart Failure
Gulinigaer Tuerhongjiang1,2, Manyun Guo1,2, Xiangrui Qiao1,2
1Department of Cardiovascular, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Insights
Heart failure is linked to gut bacteria changes and altered amino acids. This gut-amino acid-heart failure axis may impact disease progression and offer new biomarkers.
Area of Science:
- Cardiology
- Microbiology
- Metabolomics
Background:
- Heart failure (HF) incidence is increasing globally.
- Cardiometabolic disorders exacerbate cardiac dysfunction and HF progression.
- Emerging research highlights the role of gut microbiota (GM) and its metabolites in cardiovascular disease.
Purpose of the Study:
- To explore the interrelationship between amino acid (AA) metabolism and GM alterations in HF development.
- To investigate the gut-amino acid-HF axis in HF progression.
- To discuss the prognostic and therapeutic potential of this axis.
Main Methods:
- Review of existing literature on gut microbiota, amino acid metabolism, and heart failure.
- Analysis of the impact of HF-induced hypoperfusion on intestinal permeability and bacterial translocation.
- Examination of altered microbiota composition and amino acid profiles in HF patients.
Main Results:
- HF is associated with changes in gut microbiota composition and amino acid profiles.
- Increased intestinal permeability in HF allows bacterial metabolites into circulation.
- The gut-amino acid-HF axis is implicated in HF progression.
Conclusions:
- The gut-amino acid-HF axis plays a significant role in the development and progression of heart failure.
- Amino acids show potential as diagnostic and prognostic biomarkers for HF.
- Targeting the gut-amino acid-HF axis may offer novel therapeutic strategies for heart failure.
Abstract:
Heart failure (HF) is a complex clinical syndrome of which the incidence is on the rise worldwide. Cardiometabolic disorders are associated with the deterioration of cardiac function and progression of HF. Recently, there has been renewed interest in gut microbiota (GM) and its metabolites in the cardiovascular disease. HF-caused hypoperfusion could increase intestinal permeability, and a "leaky" bowel leads to bacterial translocation and make its metabolites more easily enter the circulation. Considerable evidence shows that the composition of microbiota and amino acids (AAs) has been altered in HF patients, and AAs could serve as a diagnostic and prognostic biomarker in HF. The findings indicate that the gut-amino acid-HF axis may play a key role in the progression of HF. In this paper, we focus on the interrelationship between the AA metabolism and GM alterations during the development of heart failure. We also discuss the potential prognostic and therapeutic value of the gut-amino acid-HF axis in the cortex of HF.
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