Evidence map›Paper›PMID 30658699›Full record

Trial reportArthritis research & therapy2019

In rheumatoid arthritis, changes in autoantibody levels reflect intensity of immunosuppression, not subsequent treatment response.

Emma C de Moel, Veerle F A M Derksen, Leendert A Trouw, Holger Bang, Gerard Collée, Leroy R Lard, Sofia Ramiro, Tom W J Huizinga, Cornelia F Allaart, René E M Toes and 1 more

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Arthritis research & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Review
  6. Article
  7. Autoantibodies as prognostic markers in rheumatoid arthritis.Journal of translational autoimmunity · 2025
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. B-Cell Receptor Repertoire: Recent Advances in Autoimmune Diseases.Clinical reviews in allergy & immunology · 2024
    Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
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

11 authors at 2 institutions in 1 country.

Emma C de MoelLeiden University Medical Center, Leiden, the Netherlands. e.c.de_moel@lumc.nl.ORCID 0000-0002-8940-8330
Veerle F A M DerksenLeiden University Medical Center, Leiden, the Netherlands.
Leendert A TrouwLeiden University Medical Center, Leiden, the Netherlands.
Holger BangOrgentec Diagnostika GmbH, Mainz, Germany.
Gerard ColléeHaaglanden Medical Center Antoniushove, Leidschendam, the Netherlands.
Leroy R LardHaaglanden Medical Center Antoniushove, Leidschendam, the Netherlands.
Sofia RamiroLeiden University Medical Center, Leiden, the Netherlands.
Tom W J HuizingaLeiden University Medical Center, Leiden, the Netherlands.
Cornelia F AllaartLeiden University Medical Center, Leiden, the Netherlands.
René E M ToesLeiden University Medical Center, Leiden, the Netherlands.
Diane van der WoudeLeiden University Medical Center, Leiden, the Netherlands.
Leiden University Medical Center · NLMedisch Centrum Haaglanden · NL

Funding

ZonMw 436001001
6 · The paper itself

Abstract

backgroundRheumatoid arthritis (RA) is characterized by the presence of autoantibodies like rheumatoid factor (RF), anti-cyclic citrullinated peptide-2 (anti-CCP2), and anti-carbamylated protein (anti-CarP) antibodies. It is currently unclear whether changes in autoantibody levels are associated with disease activity/treatment outcomes and whether they are modified by treatment intensity. Therefore, we determined longitudinal changes in RA-autoantibody levels, the association between these changes and activity score (DAS) and treatment outcomes, and the effect of intensity of immunosuppressive treatment on levels.

methodsIn 381 seropositive RA patients from the IMPROVED study, we measured IgG, IgM, and IgA of anti-CCP2 and anti-CarP; IgM and IgA of RF; and IgG against four citrullinated and two acetylated peptides at 4-month intervals over the first year of treatment. Following initial prednisone and methotrexate (MTX), treatment was changed every 4 months aiming for DAS < 1.6. We investigated changes in autoantibody levels following treatment escalation versus tapering, and the association of levels with DAS over time, EULAR response, and drug-free remission (DFR) ≥ 1 year.

resultsFor all 14 autoantibodies, levels decreased from 0 to 4 months and then rose until 12 months. Following treatment escalation, autoantibody levels dropped markedly, while they rose following tapering: RF IgM levels, a representative autoantibody, dropped 10% after restarting prednisone and rose 15% aU/mL after tapering MTX (p < 0.0001). There was no association between autoantibody levels and DAS over time or EULAR response. Greater relative changes between 0 and 12 months did not predict DFR (0-12-month relative change RF IgM, - 39% for no DFR (n = 126) and - 16% for DFR (n = 18)).

conclusionsChanges in RA-autoantibody levels are not associated with DAS or long-term treatment response, but reflect intensity of immunosuppression. This suggests that autoantibody levels are modifiable by current therapies, but that modifying levels is in itself of limited clinical relevance.

trial registrationISRCTN11916566 . Registered on 7 November 2006.

Indexed as

Severity of Illness IndexAdultAgedAnti-Inflammatory AgentsAntirheumatic AgentsArthritis, RheumatoidAutoantibodiesFemaleHumansImmune ToleranceMaleMethotrexateMiddle AgedOutcome Assessment, Health CarePrednisoneAnti-Inflammatory AgentsAntirheumatic AgentsAutoantibodiesMethotrexatePrednisoneAnt-CCP2Anti-carbamylated protein antibodiesAutoantibodiesDisease activityImmunosuppressionRheumatoid arthritisRheumatoid factor

Identifiers

PMID30658699
PMCPMC6339446
OpenAlexW2916745385

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.