Evidence map›Paper›PMID 39582857›Full record

ReviewFrontiers in immunology2024

The interplay between ferroptosis and inflammation: therapeutic implications for cerebral ischemia-reperfusion.

Yuxuan He, Jingyi Wang, Chunmiao Ying, Kang Li Xu, Jingwen Luo, Baiqiao Wang, Jing Gao, Zaitian Yin, Yunke Zhang

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

  1. Article
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  4. Nutrients · 2026
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  8. AgJournal of nanobiotechnology · 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

9 authors.

Yuxuan HeThe First Clinical Medical College of Henan University of Chinese Medicine, Zhengzhou, Henan, China.
Jingyi WangFaculty of Chinese Medicine of Macau University of Science and Technology, Macao, Macao SAR, China.
Chunmiao YingThe First Clinical Medical College of Henan University of Chinese Medicine, Zhengzhou, Henan, China.
Kang Li XuThe First Clinical Medical College of Henan University of Chinese Medicine, Zhengzhou, Henan, China.
Jingwen LuoFaculty of Chinese Medicine of Macau University of Science and Technology, Macao, Macao SAR, China.
Baiqiao WangThe First Clinical Medical College of Henan University of Chinese Medicine, Zhengzhou, Henan, China.
Jing GaoThe First Clinical Medical College of Henan University of Chinese Medicine, Zhengzhou, Henan, China.
Zaitian YinThe First Clinical Medical College of Henan University of Chinese Medicine, Zhengzhou, Henan, China.
Yunke ZhangThe First Clinical Medical College of Henan University of Chinese Medicine, Zhengzhou, Henan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stroke ranks as the second most significant contributor to mortality worldwide and is a major factor in disability. Ischemic strokes account for 71% of all stroke incidences globally. The foremost approach to treating ischemic stroke prioritizes quick reperfusion, involving methods such as intravenous thrombolysis and endovascular thrombectomy. These techniques can reduce disability but necessitate immediate intervention. After cerebral ischemia, inflammation rapidly arises in the vascular system, producing pro-inflammatory signals that activate immune cells, which in turn worsen neuronal injury. Following reperfusion, an overload of intracellular iron triggers the Fenton reaction, resulting in an excess of free radicals that cause lipid peroxidation and damage to cellular membranes, ultimately leading to ferroptosis. The relationship between inflammation and ferroptosis is increasingly recognized as vital in the process of cerebral ischemia-reperfusion (I/R). Inflammatory processes disturb iron balance and encourage lipid peroxidation (LPO) through neuroglial cells, while also reducing the activity of antioxidant systems, contributing to ferroptosis. Furthermore, the lipid peroxidation products generated during ferroptosis, along with damage-associated molecular patterns (DAMPs) released from ruptured cell membranes, can incite inflammation. Given the complex relationship between ferroptosis and inflammation, investigating their interaction in brain I/R is crucial for understanding disease development and creating innovative therapeutic options. Consequently, this article will provide a comprehensive introduction of the mechanisms linking ferroptosis and neuroinflammation, as well as evaluate potential treatment modalities, with the goal of presenting various insights for alleviating brain I/R injury and exploring new therapeutic avenues.

Indexed as

Brain IschemiaFerroptosisInflammationLipid PeroxidationReperfusion InjuryAnimalsHumansIronIroncerebral ischemia-reperfusionferroptosisinflammationpharmacologytherapeutic strategy

Identifiers

PMID39582857
PMCPMC11583640

What OpenQuestion holds

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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.