Evidence map›Paper›PMID 22975755›Full record

Trial reportAnnals of the rheumatic diseases2013

Markers of inflammation and bone remodelling associated with improvement in clinical response measures in psoriatic arthritis patients treated with golimumab.

Carrie L Wagner, Sudha Visvanathan, Michael Elashoff, Iain B McInnes, Philip J Mease, Gerald G Krueger, Frederick T Murphy, Kim Papp, Juan J Gomez-Reino, Michael Mack and 3 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Annals of the rheumatic diseases, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
5.1field-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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  6. Review
  7. Review
  8. Article
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  12. Adiponectin Deregulation in Systemic Autoimmune Rheumatic Diseases.International journal of molecular sciences · 2021
    Review
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  16. Review
  17. Review
  18. Golimumab for Rheumatoid Arthritis.Journal of clinical medicine · 2019
    Review
  19. Review
  20. Article
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

13 authors at 11 institutions in 6 countries.

Carrie L WagnerDepartment of Immunology, Janssen Research & Development, LLC, Spring House, PA, USA. cwagner@its.jnj.com
Sudha Visvanathan
Michael Elashoff
Iain B McInnes
Philip J Mease
Gerald G Krueger
Frederick T Murphy
Kim Papp
Juan J Gomez-Reino
Michael Mack
Anna Beutler
Dafna Gladman
Arthur Kavanaugh
University of Toronto · CAAltoona Arthritis and Osteoporosis Center · USBoehringer Ingelheim (Germany) · DEComplejo Hospitalario Universitario de Santiago · ESJanssen (Belgium) · BEProbity Medical Research · CASpringhouse · USSwedish Medical Center · USUniversity of California, San Diego · USUniversity of Glasgow · GBUniversity of Utah · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo determine serum biomarker associations with clinical response to golimumab treatment in patients with psoriatic arthritis (PsA).

methodsGO-REVEAL was a randomised, placebo-controlled study of golimumab in patients with active PsA. Samples were collected from 100 patients at baseline, week 4 and week 14, and analysed for serum-based biomarkers and protein profiling (total 92 markers); data were correlated with clinical measures at week 14.

resultsSerum levels of a subset of proteins (apolipoprotein C III, ENRAGE, IL-16, myeloperoxidase, vascular endothelial growth factor, pyridinoline, matrix metalloproteinase 3, C-reactive protein (CRP), carcinoembryonic antigen, intercellular adhesion molecule 1 and macrophage inflammatory protein 1α) at baseline or week 4 were strongly associated with American College of Rheumatology 20% improvement (ACR20) response and/or disease activity score in 28 joints (DAS28) at week 14. A smaller subset of proteins was significantly associated with a 75% improvement in the psoriasis area and severity index score (PASI75) at week 14, (adiponectin, apolipoprotein CIII, serum glutamic oxaloacetic transaminase, and tumour necrosis factor α). Subsets of proteins were identified as potentially predictive of clinical response for each of the clinical measures, and the power of these biomarker panels to predict clinical response to golimumab treatment was stronger than for CRP alone.

conclusionsThis analysis provides insight into several panels of markers that may have utility in identifying PsA patients likely to have ACR20, DAS28, or PASI75 responses following golimumab treatment.

Indexed as

AdultAntibodies, MonoclonalAntirheumatic AgentsArthritis, PsoriaticBiomarkersBone RemodelingFemaleHumansInflammationMaleMiddle AgedAntibodies, MonoclonalAntirheumatic AgentsBiomarkersgolimumab

Identifiers

PMID22975755
PMCPMC3551220
OpenAlexW2144134939

What OpenQuestion holds

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LicenceCC BY-NC
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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.