Evidence map›Paper›PMID 33461622›Full record

ArticleArthritis research & therapy2021

Serum biomarker panel for the diagnosis of rheumatoid arthritis.

Sora Mun, Jiyeong Lee, Mira Park, Jieun Shin, Mi-Kyoung Lim, Hee-Gyoo Kang

Abstract read
In one paragraph

Article in Arthritis research & therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

  1. Review
  2. SAA4: An Underdog Within the Serum Amyloid a Superfamily?International journal of molecular sciences · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Elevated Serum Amyloid A2 and A4 in Patients With Guillain-Barré Syndrome.Journal of clinical neurology (Seoul, Korea) · 2025
    Article
  10. Article
  11. Review
  12. Promoter Methylation ofAdvanced biomedical research · 2025
    Article
  13. Review
  14. Article
  15. 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

6 authors.

Sora Mun *Department of Biomedical Laboratory Science, College of Health Sciences, Eulji University, Seongnam, Republic of Korea.
Jiyeong Lee *Department of Biomedical Laboratory Science, College of Health Sciences, Eulji University, Daejeon, Republic of Korea.
Mira ParkDepartment of Preventive Medicine, School of Medicine, Eulji University, Daejeon, Republic of Korea.
Jieun ShinLiberal Arts, Woosuk University, Jeonju, Republic of Korea.
Mi-Kyoung LimDivision of Rheumatology, Department of Medicine, Eulji University School of Medicine, Daejeon, Republic of Korea.
Hee-Gyoo KangDepartment of Biomedical Laboratory Science, College of Health Sciences, Eulji University, Seongnam, Republic of Korea. kanghg@eulji.ac.kr.ORCID 0000-0001-8690-2483

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRheumatoid arthritis (RA) is an autoimmune disease of inflammatory joint damage, wherein C-reactive protein and autoantibodies including rheumatoid factor (RF) and anti-cyclic citrullinated peptide (anti-CCP) are rapidly elevated. These serological factors are diagnostic markers of RA; however, their sensitivity and specificity for prediction warrant improvement for an early and accurate diagnosis.

methodsWe aimed to identify alternative biomarkers by serum protein profiling using LC-MS/MS. We performed statistical and functional analysis of differentially expressed proteins to identify biomarker candidates complementing conventional serological tests.

resultsSeven biomarker candidates were verified through multiple reaction monitoring-based quantitative analysis, of which angiotensinogen (AGT), serum amyloid A-4 protein (SAA4), vitamin D-binding protein (VDBP), and retinol-binding protein-4 (RBP4) had an area under the curve over 0.8, thus distinguishing RA patients, including seronegative (RF- and anti-CCP-negative) RA patients, from healthy controls.

conclusionsTherefore, among seronegative RA patients, a four-biomarker panel (AGT, SAA4, VDBP, and RBP4) can prevent false negatives and help diagnose RA accurately.

Indexed as

Arthritis, RheumatoidPeptides, CyclicAutoantibodiesBiomarkersChromatography, LiquidHumansRetinol-Binding Proteins, PlasmaRheumatoid FactorSensitivity and SpecificityTandem Mass SpectrometryAutoantibodiesBiomarkersPeptides, CyclicRBP4 protein, humanRetinol-Binding Proteins, PlasmaRheumatoid FactorAngiotensinogenBiomarkersRetinol-binding protein-4Rheumatoid arthritisSerum amyloid A-4 proteinVitamin D-binding protein

Identifiers

PMID33461622
PMCPMC7812661

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Registered trials

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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.