Evidence map›Paper›PMID 39641901›Full record

ReviewCardiovascular drugs and therapy2025

Ferroptosis in Cardiovascular Diseases and Ferroptosis-Related Intervention Approaches.

Xianpeng Zhou, Hao Wang, Biao Yan, Xinwen Nie, Qingjie Chen, Xiaosong Yang, Min Lei, Xiying Guo, Changhan Ouyang, Zhanhong Ren

Abstract readReview
PubMed Publisher
In one paragraph

Review in Cardiovascular drugs and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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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

10 authors.

Xianpeng Zhou *Hubei University of Science and Technology, Xianning, 437100, Hubei, People's Republic of China.
Hao Wang *Hubei University of Science and Technology, Xianning, 437100, Hubei, People's Republic of China.
Biao Yan *Hubei University of Science and Technology, Xianning, 437100, Hubei, People's Republic of China.
Xinwen NieHubei University of Science and Technology, Xianning, 437100, Hubei, People's Republic of China.
Qingjie ChenHubei University of Science and Technology, Xianning, 437100, Hubei, People's Republic of China.
Xiaosong YangHubei University of Science and Technology, Xianning, 437100, Hubei, People's Republic of China.
Min LeiHubei University of Science and Technology, Xianning, 437100, Hubei, People's Republic of China.
Xiying GuoHubei University of Science and Technology, Xianning, 437100, Hubei, People's Republic of China.
Changhan OuyangHubei University of Science and Technology, Xianning, 437100, Hubei, People's Republic of China.
Zhanhong RenHubei University of Science and Technology, Xianning, 437100, Hubei, People's Republic of China. renzhanhong@hbust.edu.cn.

Funding

Hubei University of Science and Technology School-level Fund BK202319Hubei University of Science and Technology School-level Fund Grant No. BK202220Natural Science Foundation of Hubei Province Grant No. 2022CFB843Scientific Research and Innovation Team of Hubei University of Science and Technology Grant No. 2022T01Special Project on Diabetes and Angiopathy Grant No. 2024TNB04
6 · The paper itself

Abstract

objectiveCardiovascular diseases (CVDs) are major public health problems that threaten the lives and health of individuals. The article has reviewed recent progresses about ferroptosis and ferroptosis-related intervention approaches for the treatment of CVDs and provided more references and strategies for targeting ferroptosis to prevent and treat CVDs.

methodsA comprehensive review was conducted using the literature researches. RESULTS AND DISCUSSION: Many ferroptosis-targeted compounds and ferroptosis-related genes may be prospective targets for treating CVDs and our review provides a solid foundation for further studies about the detailed pathological mechanisms of CVDs.

conclusionThere are challenges and limitations about the translation of ferroptosis-targeted potential therapies from experimental research to clinical practice. It warrants further exploration to pursure safer and more effective ferroptosis-targeted thereapeutic approaches for CVDs.

Indexed as

Cardiovascular AgentsCardiovascular DiseasesFerroptosisAnimalsHumansMolecular Targeted TherapySignal TransductionCardiovascular AgentsAmino acid metabolismCardiovascular diseasesFerroptosisIron metabolismLipid metabolism

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.