# The tryptophan-kynurenine pathway in cardiovascular diseases: mechanistic insights and therapeutic opportunities

**Authors:** Wei Chen, Min Shui, Zhen Wei, Weiyan Gao, Xin Liu, Qian Lei

PMC · DOI: 10.3389/fcvm.2026.1726522 · 2026-03-11

## TL;DR

This review explores how the tryptophan-kynurenine pathway contributes to cardiovascular diseases and highlights its potential for new diagnostics and treatments.

## Contribution

The paper systematically reviews the role of the kynurenine pathway in CVDs and its potential as a therapeutic target.

## Key findings

- Dysregulated kynurenine pathway metabolites are linked to heart failure, atherosclerosis, and hypertension.
- KP metabolites influence immune activation, inflammation, and endothelial dysfunction in CVDs.
- Metabolomics and AI could enhance CVD diagnosis and therapeutic development.

## Abstract

Cardiovascular diseases (CVDs) are the leading cause of death worldwide, making them crucial to further explore their mechanisms. Beyond traditional risk factors, disturbances in tryptophan metabolism, particularly the imbalance in the kynurenine pathway (KP) which accounts for over 95% of metabolic flux—have garnered significant attention in cardiovascular research. In the human body, tryptophan is primarily metabolized through the KP. This process is catalyzed by key enzymes, indoleamine 2,3-dioxygenase and tryptophan 2,3-dioxygenase, which convert tryptophan into kynurenine and further downstream metabolites such as kynurenic acid and 3-hydroxykynurenine. Studies have shown that levels of multiple key metabolites in KP are dysregulated in patients with CVDs, and by participating in processes such as immune activation, inflammatory responses, reactive oxygen species production, and endothelial dysfunction, and they play a complex role in mediating the pathophysiology of various CVDs, including heart failure, atherosclerosis, and hypertension. This review will systematically outline the physiology of tryptophan metabolism and the KP, summarize how key enzymes and metabolites regulate CVDs, and explore their potential as novel biomarkers for early diagnosis and prognosis and as therapeutic targets. Additionally, the review will discuss the future applications of metabolomics and artificial intelligence in the diagnosis of CVDs and the development of new therapeutics, aiming to provide new perspectives for the prevention and treatment of CVDs.

## Linked entities

- **Chemicals:** tryptophan (PubChem CID 1148), kynurenine (PubChem CID 846), kynurenic acid (PubChem CID 3845), 3-hydroxykynurenine (PubChem CID 89)
- **Diseases:** heart failure (MONDO:0005252), atherosclerosis (MONDO:0005311)

## Full-text entities

- **Genes:** TDO2 (tryptophan 2,3-dioxygenase) [NCBI Gene 6999] {aka HYPTRP, TDO, TO, TPH2, TRPO}
- **Diseases:** inflammatory (MESH:D007249), hypertension (MESH:D006973), heart failure (MESH:D006333), atherosclerosis (MESH:D050197), CVDs (MESH:D002318), death (MESH:D003643)
- **Chemicals:** 3-hydroxykynurenine (MESH:C005045), kynurenine (MESH:D007737), kynurenic acid (MESH:D007736), reactive oxygen species (MESH:D017382), tryptophan (MESH:D014364)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13013489/full.md

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Source: https://tomesphere.com/paper/PMC13013489