Evidence map›Paper›PMID 37520558›Full record

SynthesisFrontiers in immunology2023

Crosstalk between ferroptosis and chondrocytes in osteoarthritis: a systematic review of

Siyang Cao, Yihao Wei, Huihui Xu, Jian Weng, Tiantian Qi, Fei Yu, Su Liu, Ao Xiong, Peng Liu, Hui Zeng

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis 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 25 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 3 pooled it
5.7field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 3 syntheses or guidelines pooled it, 24 citations in OpenAlex.

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  13. Ginsenoside Rg5 mitigates tenocyte deathJournal of ginseng research · 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

10 authors at 1 institution in 1 country.

Siyang CaoDepartment of Bone & Joint Surgery, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
Yihao WeiDepartment of Bone & Joint Surgery, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
Huihui XuDepartment of Bone & Joint Surgery, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
Jian WengDepartment of Bone & Joint Surgery, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
Tiantian QiDepartment of Bone & Joint Surgery, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
Fei YuDepartment of Bone & Joint Surgery, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
Su LiuDepartment of Bone & Joint Surgery, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
Ao XiongDepartment of Bone & Joint Surgery, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
Peng LiuDepartment of Bone & Joint Surgery, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
Hui ZengDepartment of Bone & Joint Surgery, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China.
Peking University Shenzhen Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Recent scientific reports have revealed a close association between ferroptosis and the occurrence and development of osteoarthritis (OA). Nevertheless, the precise mechanisms by which ferroptosis influences OA and how to hobble OA progression by inhibiting chondrocyte ferroptosis have not yet been fully elucidated. This study aims to conduct a comprehensive systematic review (SR) to address these gaps. Methods: Following the guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020, we conducted a comprehensive search of the Embase, Ovid, ProQuest, PubMed, Scopus, the Cochrane Library, and Web of Science databases to identify relevant studies that investigate the association between ferroptosis and chondrocytes in OA. Our search included studies published from the inception of these databases until January 31st, 2023. Only studies that met the predetermined quality criteria were included in this SR. Results: In this comprehensive SR, a total of 21 studies that met the specified criteria were considered suitable and included in the current updated synthesis. The mechanisms underlying chondrocyte ferroptosis and its association with OA progression involve various biological phenomena, including mitochondrial dysfunction, dysregulated iron metabolism, oxidative stress, and crucial signaling pathways. Conclusion: Ferroptosis in chondrocytes has opened an entirely new chapter for the investigation of OA, and targeted regulation of it is springing up as an attractive and promising therapeutic tactic for OA. Systematic review registration: https://inplasy.com/inplasy-2023-3-0044/, identifier INPLASY202330044.

Indexed as

FerroptosisOsteoarthritisChondrocytesHumansOxidative StressSignal Transductionchondrocytescrosstalkferroptosisosteoarthritissystematic review

Identifiers

PMID37520558
PMCPMC10376718
OpenAlexW4384483757

What Socratic 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 Socratic graph.