Evidence map›Paper›PMID 36267583›Full record

ReviewFrontiers in physiology2022

Advancement in understanding the role of ferroptosis in rheumatoid arthritis.

Li Long, Hongmei Guo, Xixi Chen, Yan Liu, Ruyi Wang, Xiaomei Zheng, Xiaobo Huang, Qiao Zhou, Yi Wang

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

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  11. Clinical significance of long non-coding RNA NORAD in rheumatoid arthritis.Advances in rheumatology (London, England) · 2024
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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 at 1 institution in 1 country.

Li LongDepartment of Rheumatology and Immunology, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, China.
Hongmei GuoDepartment of Rheumatology and Immunology, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, China.
Xixi ChenDepartment of Rheumatology and Immunology, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, China.
Yan LiuDepartment of Rheumatology and Immunology, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, China.
Ruyi WangDepartment of Rheumatology and Immunology, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, China.
Xiaomei ZhengDepartment of Rheumatology and Immunology, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, China.
Xiaobo HuangDepartment of Critical Care Medicine, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, China.
Qiao ZhouDepartment of Rheumatology and Immunology, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, China.
Yi WangDepartment of Critical Care Medicine, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, China.
Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is a chronic, systemic disease of unknown etiology. The primary manifestation of RA is inflammatory synovitis, which eventually leads to deformity and functional loss. Ferroptosis is a non-apoptosis form of cell death that depends on intracellular iron accumulation. This leads to an increase in reactive oxygen species (ROS) induced-lipid peroxidation. The underlying mechanisms of ferroptosis are System Xc- and Glutathione metabolism, regulation of glutathione peroxidase 4 activity, and ROS generation. Recent studies have shown an association between the pathogenesis of RA and ferroptosis, suggesting the involvement of ferroptosis in the onset and progression of RA. In this review, we have focused on the mechanism of ferroptosis and its association with RA pathogenesis. Further, we discuss the status of therapeutics targeting ferroptosis in the treatment of patients with RA. Targeting ferroptosis could be a potential therapeutic approach for RA treatment.

Indexed as

ferroptosisglutathione (GSH) metabolismlipid peroxidationpathogenesisreactive oxygen speciesrheumatoid arthritis

Identifiers

PMID36267583
PMCPMC9576928
OpenAlexW4301398094

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.