Evidence map›Paper›PMID 41890877›Full record

ReviewFrontiers in cardiovascular medicine2026

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

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

Abstract readReview
In one paragraph

Review in Frontiers in cardiovascular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. UntargetedNutrients · 2026
    Trial
  2. Article
  3. Review
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Wei ChenDepartment of Anesthesiology, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Min ShuiDepartment of Anesthesiology, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Zhen WeiDepartment of Anesthesiology, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Weiyan GaoDepartment of Anesthesiology, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Xin LiuDepartment of Anesthesiology, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Qian LeiDepartment of Anesthesiology, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

cardiovascular diseaseskynurenine pathwaymetabolomicstreatmenttryptophan metabolism

Identifiers

PMID41890877
PMCPMC13013489

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.