Evidence map›Paper›PMID 38111578›Full record

ReviewFrontiers in immunology2023

Ferroptosis: an important player in the inflammatory response in diabetic nephropathy.

Jialing Li, Luxin Li, Zhen Zhang, Peijian Chen, Haiying Shu, Can Yang, Yanhui Chu, Jieting Liu

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
15.8field-weighted citation impact, top 1% of its field
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

46 citing papers in PubMed, 61 citations in OpenAlex.

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  8. Immune Aging as a Failure of Programmed Cell Death Coordination.International journal of molecular sciences · 2026
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  11. The role of ferroptosis in vascular endothelial cells and its role in the pathogenesis of cervical spondylosis of vertebral artery type: a comprehensive review.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas · 2026
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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

8 authors at 1 institution in 1 country.

Jialing Li *College of Life Sciences, Mudanjiang Medical University, Mudanjiang, China.
Luxin Li *College of Life Sciences, Mudanjiang Medical University, Mudanjiang, China.
Zhen Zhang *Heilongjiang Key Laboratory of Anti-Fibrosis Biotherapy, Mudanjiang Medical University, Mudanjiang, China.
Peijian ChenCollege of Life Sciences, Mudanjiang Medical University, Mudanjiang, China.
Haiying ShuCollege of Life Sciences, Mudanjiang Medical University, Mudanjiang, China.
Can YangCollege of Life Sciences, Mudanjiang Medical University, Mudanjiang, China.
Yanhui ChuCollege of Life Sciences, Mudanjiang Medical University, Mudanjiang, China.
Jieting LiuCollege of Life Sciences, Mudanjiang Medical University, Mudanjiang, China.
Mudanjiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic nephropathy (DN) is a chronic inflammatory disease that affects millions of diabetic patients worldwide. The key to treating of DN is early diagnosis and prevention. Once the patient enters the clinical proteinuria stage, renal damage is difficult to reverse. Therefore, developing early treatment methods is critical. DN pathogenesis results from various factors, among which the immune response and inflammation play major roles. Ferroptosis is a newly discovered type of programmed cell death characterized by iron-dependent lipid peroxidation and excessive ROS production. Recent studies have demonstrated that inflammation activation is closely related to the occurrence and development of ferroptosis. Moreover, hyperglycemia induces iron overload, lipid peroxidation, oxidative stress, inflammation, and renal fibrosis, all of which are related to DN pathogenesis, indicating that ferroptosis plays a key role in the development of DN. Therefore, this review focuses on the regulatory mechanisms of ferroptosis, and the mutual regulatory processes involved in the occurrence and development of DN and inflammation. By discussing and analyzing the relationship between ferroptosis and inflammation in the occurrence and development of DN, we can deepen our understanding of DN pathogenesis and develop new therapeutics targeting ferroptosis or inflammation-related regulatory mechanisms for patients with DN.

Indexed as

Diabetes MellitusDiabetic NephropathiesFerroptosisHumansInflammationKidneyOxidative Stressdiabetic nephropathyferroptosisinflammationoxidative stresssignaling pathway

Identifiers

PMID38111578
PMCPMC10725962
OpenAlexW4389301829

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.