Evidence map›Paper›PMID 32461558›Full record

ArticleExperimental & molecular medicine2020

Angiogenic cytokines can reflect the synovitis severity and treatment response to biologics in rheumatoid arthritis.

Ji-Won Kim, Jin-Sun Kong, Saseong Lee, Seung-Ah Yoo, Jung Hee Koh, Jingchun Jin, Wan-Uk Kim

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 3% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
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  5. Review
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  7. Article
  8. Pathogenic Role of Cytokines in Rheumatoid Arthritis.Journal of clinical medicine · 2025
    Review
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  10. Article
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  14. Article
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  16. Alcohol extracts fromMolecular medicine reports · 2023
    Article
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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

7 authors at 3 institutions in 2 countries.

Ji-Won KimDivision of Rheumatology, Department of Internal Medicine, Catholic University of Daegu School of Medicine, Daegu, Korea.ORCID http://orcid.org/0000-0002-0498-5762
Jin-Sun KongDepartment of Biomedicine and Health Sciences, The Catholic University of Korea, Seoul, Korea.
Saseong LeeDepartment of Biomedicine and Health Sciences, The Catholic University of Korea, Seoul, Korea.
Seung-Ah YooDepartment of Biomedicine and Health Sciences, The Catholic University of Korea, Seoul, Korea.
Jung Hee KohDivision of Rheumatology, Department of Internal Medicine, The Catholic University of Korea, Seoul, Korea.ORCID http://orcid.org/0000-0002-6617-1449
Jingchun JinDepartment of Immunology of Yanbian University Hospital, 133000, Yanji, Jilin Province, China.
Wan-Uk KimDepartment of Biomedicine and Health Sciences, The Catholic University of Korea, Seoul, Korea. wan725@catholic.ac.kr.ORCID http://orcid.org/0000-0001-8224-8496
Catholic University of Korea · KRDaegu Catholic University · KRYanbian University of Science and Technology · CN

Funding

National Research Foundation of Korea (NRF) 2015R1A3A2032927National Research Foundation of Korea (NRF) 2018R1D1A1B07045491
6 · The paper itself

Abstract

Angiogenesis and synoviocyte hyperplasia, called 'pannus,' are pathologic hallmarks of rheumatoid arthritis (RA). To determine the clinical significance of angiogenic cytokines in RA, the levels of pro-angiogenic cytokines, including VEGF, placenta growth factor (PlGF), and IL-6, were measured in the synovial fluid (SF, n = 54) and sera of RA patients (n = 157) using ELISA. Patients (n = 103) with disease activity score 28 (DAS28) > 3.2, which indicates moderate to high RA activity, underwent follow-up blood sampling at 6 months after treatment with conventional disease-modifying anti-rheumatic drugs (c-DMARD) or biologic DMARD (b-DMARD) including an anti-TNFα antibody, an anti-IL-6 antibody, and abatacept. Ultrasonography (US) was performed on affected joints to define the synovitis severity at the time of sampling. Consequently, in the SF of RA patients, PlGF and IL-6 levels correlated well with synovitis severity determined by US. In RA sera, VEGF and IL-6 levels were elevated in proportion to synovitis severity, correlating with conventional markers for disease activity, including ESR, CRP, and DAS28. In c-DMARD users (n = 53), serially monitored levels of serum VEGF, IL-6, erythrocyte sedimentation rate (ESR), and C-reactive protein (CRP) all decreased in good and moderate responders but not in nonresponders. In b-DMARD users (n = 49), only serum VEGF well represented the treatment response, while CRP nonspecifically decreased irrespective of the treatment outcome. By multivariable analysis, serum ΔVEGF, but not ΔESR or ΔCRP, was an independent factor associated with good and moderate responses to DMARD. In summary, the angiogenic cytokines PlGF and VEGF represent the synovitis severity of RA assessed by US. In patients receiving b-DMARD, serum VEGF may be more valuable than CRP in reflecting the treatment response.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidBiological ProductsBiomarkersCytokinesHumansInflammation MediatorsNeovascularization, PathologicSeverity of Illness IndexSynovitisTreatment OutcomeAntirheumatic AgentsBiological ProductsBiomarkersCytokinesInflammation Mediators

Identifiers

PMID32461558
PMCPMC7272442
OpenAlexW3030141001

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.