# Dietary Nutrients, Gut Microbiota, and Cardiac Function: From Metabolic Mechanisms to Clinical Applications

**Authors:** Lucia Scisciola, Manuela Giovanna Basilicata, Marta Belmonte, Ada Pesapane, Rosaria Anna Fontanella, Nunzia Balzano, Alberta Maria Maddalena Palazzo, Rashmi Joshi, Asad Zia, Giovanni Tortorella, Zeeshan Ulfat, Maryam Arshad, Giuseppe Paolisso

PMC · DOI: 10.3390/nu18030467 · Nutrients · 2026-01-31

## TL;DR

This paper explores how gut microbiota metabolites influence heart function and how diet can shape these effects for cardiovascular health.

## Contribution

It integrates preclinical, clinical, and genetic evidence to highlight the diet–microbiota–metabolite axis as a novel pathway for cardiometabolic protection.

## Key findings

- Gut-derived metabolites like TMAO and PAGln are linked to adverse cardiovascular outcomes.
- SCFAs and indole derivatives may offer protective effects on the heart.
- Dietary patterns rich in fiber and plant-based nutrients support beneficial metabolite profiles.

## Abstract

Background: The heart depends on a continuous and flexible energy supply from fatty acids, glucose, and other substrates. Emerging evidence shows that gut microbiota-derived metabolites—such as trimethylamine-N-oxide (TMAO), short-chain fatty acids (SCFAs), secondary bile acids, indoles, phenylacetylglutamine (PAGln), and branched-chain amino acids—modulate cardiac metabolism and function. Although clinical evidence linking these metabolites to cardiovascular outcomes is expanding, most data remain associative, with limited causal or interventional proof. Methods: A comprehensive narrative review was conducted (PubMed 2010–2025) to integrate preclinical, clinical, and Mendelian randomization studies on microbiota-derived metabolites and cardiovascular disease, complemented by evidence from dietary and interventional trials. Results: Gut-derived metabolites regulate mitochondrial energetics, inflammatory, immune system, and oxidative pathways, and endothelial and platelet activation. Elevated plasma TMAO and PAGln levels are often associated with adverse cardiovascular outcomes, while SCFAs and indole derivatives may related to protective effects. However, findings across cohorts remain heterogeneous, largely due to differences in diet, renal function, and analytical methods. Dietary patterns rich in fiber and plant-based nutrients favor beneficial metabolite profiles, underscoring the nutritional modulation of the gut–heart axis. Conclusions: The diet–microbiota–metabolite axis represents an emerging pathway connecting nutrition to cardiovascular health. Translating this knowledge into prevention and therapy will require large-scale randomized studies and integrated multi-omics approaches. Dietary modulation of microbial metabolism may ultimately become a novel strategy for cardiometabolic protection.

## Linked entities

- **Chemicals:** trimethylamine-N-oxide (PubChem CID 1145), indoles (PubChem CID 139191468), phenylacetylglutamine (PubChem CID 92258), branched-chain amino acids (PubChem CID 9886134)
- **Diseases:** cardiovascular disease (MONDO:0004995)

## Full-text entities

- **Diseases:** cardiovascular disease (MESH:D002318), inflammatory (MESH:D007249)
- **Chemicals:** glucose (MESH:D005947), fatty acids (MESH:D005227), SCFAs (MESH:D005232), PAGln (MESH:C003089), trimethylamine-N-oxide (MESH:C005855), branched-chain amino acids (MESH:D000597), TMAO (-), indoles (MESH:D007211), bile acids (MESH:D001647)

## Full text

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## Figures

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## References

139 references — full list in the complete paper: https://tomesphere.com/paper/PMC12899627/full.md

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Source: https://tomesphere.com/paper/PMC12899627