Key result
Gut microbiota dysbiosis and metabolites like TMAO are linked to the development and progression of HF.
Why the study?
To summarize current evidence regarding the gut microbiota as an emerging cardiovascular risk factor in heart failure, focusing on biological mechanisms and clinical and epidemiological evidence.
The gut-heart axis represents a novel paradigm in heart failure pathophysiology, highlighting the microbiome as a potential therapeutic target, though current evidence is largely observational.
Microbiome modulation merits investigation as a heart failure target; leaves open whether it improves clinical outcomes.
In recent years, gut microbiota has emerged as a central modulator of cardiovascular health and disease. This has led to a transition from the old understanding of cardiovascular pathology as a largely cardiac-centric problem to a systemic, multi-organ process. A growing body of evidence demonstrates that changes in the makeup of gut microbes, generally called dysbiosis, are significant in the development and progression of cardiovascular illnesses, including heart failure. Moreover, there are bidirectional interactions between the failing heart and the gut. In heart failure, impaired hemodynamics and venous congestion further worsen intestinal hypoperfusion and barrier dysfunction in a self-perpetuating cycle that exacerbates dysbiosis and systemic inflammation. The gut–heart axis offers a fresh paradigm for illness progression beyond classical neurohormonal and hemodynamic processes. The gut microbiota acts as an endocrine organ by producing bioactive metabolites such as TMAO (trimethylamine N-oxide), SCFA (short-chain fatty acids) and bile acids, which, via several routes, have a serious impact on host health and disease. This narrative review aims to summarize the current evidence for the gut microbiota as a new cardiovascular risk factor, focusing on biological mechanisms and clinical and epidemiological evidence.
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David et al. (2026) conducted a review in Heart failure. Gut microbiota dysbiosis was evaluated. Gut microbiota dysbiosis and its metabolites, such as TMAO and short-chain fatty acids, are increasingly recognized as potential contributors to the development and progression of heart failure.
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