Evidence map›Paper›PMID 33168080›Full record

ArticleArthritis research & therapy2020

Gene expression identifies patients who develop inflammatory arthritis in a clinically suspect arthralgia cohort.

Ellis Niemantsverdriet, Erik B van den Akker, Debbie M Boeters, Susan J F van den Eeden, Annemieke Geluk, Annette H M van der Helm-van Mil

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
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  7. An ElevatedCurrent issues in molecular biology · 2024
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  9. Obesity phenotypes related to musculoskeletal disorders; a cross-sectional study from RaNCD cohort.Archives of public health = Archives belges de sante publique · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Ellis NiemantsverdrietDepartment of Rheumatology, Leiden University Medical Center, PO Box 9600, Leiden, 2300 RC, The Netherlands. e.niemantsverdriet@lumc.nl.ORCID http://orcid.org/0000-0002-5781-3817
Erik B van den AkkerDepartment of Biomedical Data Sciences, Leiden University Medical Center, Leiden, The Netherlands.
Debbie M BoetersDepartment of Rheumatology, Leiden University Medical Center, PO Box 9600, Leiden, 2300 RC, The Netherlands.
Susan J F van den EedenDepartment of Infectious Diseases/Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, The Netherlands.
Annemieke GelukDepartment of Infectious Diseases/Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, The Netherlands.
Annette H M van der Helm-van MilDepartment of Rheumatology, Leiden University Medical Center, PO Box 9600, Leiden, 2300 RC, The Netherlands.
Leiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEstablished rheumatoid arthritis (RA) patients display differentially expressed genes coding for cytokine/chemokine-mediated immunity compared to healthy controls. It is unclear, however, if in the pre-arthritis phase of clinically suspect arthralgia (CSA) expression of immune genes differ between patients who do or do not develop clinically evident inflammatory arthritis (IA).

methodsTwo hundred thirty-six consecutive patients presenting with arthralgia clinically suspected for progression to RA were followed until IA development or else for median 24 months (IQR 12-26). Baseline whole blood RNA expression was determined for a previously identified set of 133 genes associated with the innate and adaptive immune system by dual-color reverse-transcription multiplex ligation-dependent probe amplification (dcRT-MLPA) profiling. Cox proportional hazard models were used.

resultsTwenty percent of CSA patients developed IA. After correction for multiple testing, expression levels of six genes (IFNG, PHEX, IGF-1, IL-7R, CD19, CCR7) at the time of presentation were associated with progression to IA. PHEX and IGF-1 were highly correlated with each other (ρ = 0.97). In multivariable analysis correcting for the different genes, expressions of IL-7R and IGF-1 were independently associated with IA development (p = 0.025, p = 0.046, respectively). Moreover, IL-7R and IGF-1 remained significantly associated even after correction for known predictors (ACPA, CRP, imaging-detected subclinical joint inflammation; p = 0.039, p = 0.005, respectively). These genes are also associated with RA development.

conclusionsIL-7R and IGF-1 were differentially expressed between CSA patients who did or did not progress to IA, independent from regularly used predictors. These biomarkers may become helpful in prognostication of CSA patients. Furthermore, because both genes are associated with T cell functioning, T cell dysregulation may mediate progression from arthralgia to arthritis.

Indexed as

ArthralgiaArthritis, RheumatoidGene ExpressionCohort StudiesDisease ProgressionHumansClinically suspect arthralgiaGene expressionInflammatory arthritisMLPARNA

Identifiers

PMID33168080
PMCPMC7653888
OpenAlexW3101219333

What OpenQuestion holds

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LicenceCC BY
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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.