Evidence map›Paper›PMID 32669451›Full record

ArticleRMD open2020

Achieving sustained minimal disease activity with methotrexate in early interleukin 23-driven early psoriatic arthritis.

Hannah den Braanker, Kim Wervers, Adriana M C Mus, Priyanka S Bangoer, Nadine Davelaar, Jolanda Luime, Ilja Tchetverikov, J M W Hazes, Marijn Vis, Erik Lubberts and 1 more

Open access · goldAbstract read
In one paragraph

Article in RMD open, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Observational
  5. 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 3 institutions in 1 country.

Hannah den Braanker *Department of Rheumatology and Clinical Immunology, Maasstad Hospital, Rotterdam, Netherlands.ORCID 0000-0003-4618-6827
Kim Wervers *Department of Rheumatology, Erasmus Medical Centre, Rotterdam, Netherlands.
Adriana M C MusDepartment of Rheumatology, Erasmus Medical Centre, Rotterdam, Netherlands.
Priyanka S BangoerDepartment of Rheumatology, Erasmus Medical Centre, Rotterdam, Netherlands.
Nadine DavelaarDepartment of Rheumatology, Erasmus Medical Centre, Rotterdam, Netherlands.
Jolanda LuimeDepartment of Rheumatology, Erasmus Medical Centre, Rotterdam, Netherlands.
Ilja TchetverikovDepartment of Rheumatology, Albert Schweitzer Ziekenhuis, Dordrecht, Netherlands.
J M W HazesDepartment of Rheumatology, Erasmus Medical Centre, Rotterdam, Netherlands.
Marijn VisDepartment of Rheumatology, Erasmus Medical Centre, Rotterdam, Netherlands.
Erik LubbertsDepartment of Rheumatology, Erasmus Medical Centre, Rotterdam, Netherlands.
Marc R KokDepartment of Rheumatology and Clinical Immunology, Maasstad Hospital, Rotterdam, Netherlands KokMR@maasstadziekenhuis.nl.
Erasmus University Rotterdam · NLMaasstad Ziekenhuis · NLAlbert Schweitzer Ziekenhuis · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesMethotrexate (MTX) is currently the recommended first-line therapy for treating psoriatic arthritis (PsA), despite lacking clear evidence. No estimates of efficacy of MTX in usual care and no clear MTX responsive clinical or laboratory variables are currently available. This study describes the response to MTX monotherapy in newly diagnosed patients with PsA in usual care. Second, we compared clinical variables and cytokine profiles in patients responding and not responding to MTX monotherapy.

methodsWe used data collected in the Dutch southwest Early Psoriatic Arthritis cohoRt study to select patients with PsA with oligoarthritis or polyarthritis, and at least 1 year follow-up. We analysed disease activity at 6 months of patients who started MTX monotherapy and still used MTX monotherapy 1 year after diagnosis. Cytokine profiles were determined at baseline and after 3 and 6 months with a bead-based multi-immunoassay.

resultsWe identified 219 patients of which 183 (84%) patients started MTX monotherapy within 6 months after diagnosis. 90 patients used MTX monotherapy throughout the first year of which 44 patients (24%) reached minimal disease activity(MDA) at 6 months, decreasing to 33 patients (18%) after 1 year. Non-responders had significantly higher concentrations of interleukin (IL) 23 and IL-10 before and during MTX therapy.

conclusionsOur results showed that only 18% of patients with PsA are in sustained MDA after 1 year of MTX monotherapy and non-responders more often had IL-23-driven disease. Our results indicate the need for more treat-to-target and personalised therapy strategies in PsA.

Indexed as

AdultAgedAntirheumatic AgentsArthritis, PsoriaticBiomarkersCytokinesFemaleHumansInflammation MediatorsInterleukin-23MaleMethotrexateMiddle AgedPrognosisSeverity of Illness IndexTreatment OutcomeAntirheumatic AgentsBiomarkersCytokinesInflammation MediatorsInterleukin-23MethotrexateCytokinesEpidemiologyMethotrexatePsoriatic Arthritis

Identifiers

PMID32669451
PMCPMC7425114
OpenAlexW3042275248

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.