Evidence map›Paper›PMID 34880852›Full record

ArticleFrontiers in immunology2021

Mechanism of Hip Arthropathy in Ankylosing Spondylitis: Abnormal Myeloperoxidase and Phagosome.

Chaojie Yu, Xinli Zhan, Tuo Liang, Liyi Chen, Zide Zhang, Jie Jiang, Jiang Xue, Jiarui Chen, Chong Liu

Open access · goldAbstract readComparative Study
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

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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 2 institutions in 1 country.

Chaojie YuSpine and Osteopathy Ward, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Xinli ZhanSpine and Osteopathy Ward, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Tuo LiangSpine and Osteopathy Ward, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Liyi ChenSpine and Osteopathy Ward, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Zide ZhangSpine and Osteopathy Ward, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Jie JiangSpine and Osteopathy Ward, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Jiang XueSpine and Osteopathy Ward, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Jiarui ChenSpine and Osteopathy Ward, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Chong LiuSpine and Osteopathy Ward, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
First Affiliated Hospital of GuangXi Medical University · CNGuangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The pathogenesis of Ankylosing spondylitis (AS) has not been elucidated, especially involving hip joint disease. The purpose of this study was to analyze the proteome of diseased hip in AS and to identify key protein biomarkers. Material and Methods: We used label-free quantification combined with liquid chromatography mass spectrometry (LC-MS/MS) to screen for differentially expressed proteins in hip ligament samples between AS and No-AS groups. Key protein was screened by Bioinformatics methods. and verified by Results: There were 3,755 identified proteins, of which 92.916% were quantified. A total of 193 DEPs (49 upregulated proteins and 144 downregulated proteins) were identified according to P < 0.01 and Log|FC| > 1. DEPs were mainly involved in cell compartment, including the vacuolar lumen, azurophil granule, primary lysosome, etc. The main KEGG pathway included Phagosome, Glycerophospholipid metabolism, Lysine degradation, Pentose phosphate pathway. Myeloperoxidase (MPO) was identified as a key protein involved in Phagosome pathway. The experiment of siRNA interfering with cells further confirmed that the upregulated MPO may promote the inflammatory response of fibroblasts. Conclusions: The overexpression of MPO may contribute to the autoimmune inflammatory response of AS-affected hip joint through the phagosome pathway.

Indexed as

ProteomeAdultBiomarkersCells, CulturedComputational BiologyFemaleFibroblastsGene Expression RegulationGene OntologyHumansLigamentsMaleMiddle AgedOsteoarthritis, HipPeroxidasePhagosomesBiomarkersMPO protein, humanPeroxidaseProteomeRNA, Small Interferingankylosing spondylitisbioinformaticsmyeloperoxidasephagosomeproteomics

Identifiers

PMID34880852
PMCPMC8647161
OpenAlexW3215702502

What OpenQuestion holds

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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.