Evidence map›Paper›PMID 31730497›Full record

Observational studyArthritis research & therapy2019

Predictors of good response to conventional synthetic DMARDs in early seronegative rheumatoid arthritis: data from the ESPOIR cohort.

Cédric Lukas, Julia Mary, Michel Debandt, Claire Daïen, Jacques Morel, Alain Cantagrel, Bruno Fautrel, Bernard Combe

Registry-linked trialOpen access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Arthritis research & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03666091 (Etude et Suivi Des POlyarthrites Indifférenciées Récentes), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.2field-weighted citation impact, top 12% 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.

NCT03666091 completednot on this map

Etude et Suivi Des POlyarthrites Indifférenciées Récentes

TypeobservationalSponsorSociete Francaise de RhumatologieRan2002 to 2025Enrolled813ConditionsEarly Rheumatoid Arthritis or Early Undiffentiated Arthritis
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

8 authors at 4 institutions in 2 countries.

Cédric LukasRheumatology Department, CHU Montpellier, Montpellier University, Montpellier, France. c-lukas@chu-montpellier.fr.ORCID 0000-0002-1095-3492
Julia MaryRheumatology Department, CHU Martinique, Pierre Zobda-Quitman Hospital, 97200, Fort-de-France, Martinique, French West Indies, France.
Michel DebandtRheumatology Department, CHU Martinique, Pierre Zobda-Quitman Hospital, 97200, Fort-de-France, Martinique, French West Indies, France.
Claire DaïenRheumatology Department, CHU Montpellier, Montpellier University, Montpellier, France.
Jacques MorelRheumatology Department, CHU Montpellier, Montpellier University, Montpellier, France.
Alain CantagrelRheumatology Department, University Paul Sabatier Toulouse III, Purpan Hospital, 31059, Toulouse, France.
Bruno FautrelSorbonne Université, Institut Pierre Louis d'Epidémiologie et Santé Publique, INSERM UMR S 1136, AP-HP, Groupe hospitalier Pitié Salpêtrière, Service de Rhumatologie, Paris, France.
Bernard CombeRheumatology Department, CHU Montpellier, Montpellier University, Montpellier, France.
Université de Montpellier · FRCentre Hospitalier Universitaire de Martinique · MQInserm · FRUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveEarly seronegative rheumatoid arthritis (RA) is considered a specific entity, especially regarding diagnostic issues and prognosis. Little is known about its potentially different initial clinical presentation and outcome. We aimed to determine predictors of good response to conventional synthetic disease-modifying anti-rheumatic drugs (csDMARDs) in seronegative RA patients with early inflammatory arthritis. PATIENTS AND

methodsPatients from the ESPOIR cohort with early inflammatory arthritis fulfilling the 2010 ACR/EULAR classification criteria for RA despite negativity for both rheumatoid factor and anti-CCP antibodies. The primary endpoint was a good or moderate EULAR response assessed after 1 year of follow-up, given at least 3 months of treatment with a csDMARD. Secondary objectives were to compare the early therapeutic response to methotrexate (MTX) and leflunomide (LEF) versus other csDMARDs (hydroxychloroquine, sulfasalazine) and to identify factors associated with functional disability (Health Assessment Questionnaire-Disability Index [HAQ-DI] > 0.5 at 1 year) and structural progression (van der Heijde-modified total Sharp score > 1 and > 5 points at 1 year). Logistic regression analysis was used to determine independent predictors of outcomes.

resultsOne hundred seventy-two patients were analyzed. Overall, 98/172 (57%) patients received MTX during the first year of follow-up. A good or moderate EULAR response at 1 year was associated with early use of csDMARDs (i.e., within 3 months after the first joint swelling) on univariate and multivariable analysis (odds ratio = 2.41 [95% confidence interval 1.07-5.42], p = 0.03). Response rates were not affected by other classical prognostic factors (i.e., baseline DAS28). Presence of erosions at baseline was associated with Sharp score progression > 1 point and > 5 points (both p = 0.03) at 1 year. HAQ-DI ≥ 1 at inclusion and active smoking were significantly associated with HAQ-DI > 0.5 at 1 year.

conclusionOur results suggest that delay in initiation of csDMARD more than baseline clinical, biological, or imaging features predominantly affects the outcome in early seronegative RA. These findings confirm that the usual therapeutic concepts in RA (early treatment, tight control, and treat-to-target) should be applied similarly to both seropositive and seronegative disease forms.

trial registrationClinicalTrials.gov: NCT03666091. Registered September 11, 2018.

Indexed as

AdultAnti-Citrullinated Protein AntibodiesAntirheumatic AgentsArthritis, RheumatoidCohort StudiesDisability EvaluationDrug Therapy, CombinationFemaleHumansHydroxychloroquineImmunosuppressive AgentsLeflunomideMaleMethotrexateMiddle AgedPrognosisAnti-Citrullinated Protein AntibodiesAntirheumatic AgentsHydroxychloroquineImmunosuppressive AgentsLeflunomideMethotrexateRheumatoid FactorSulfasalazineDMARDESPOIR cohortRheumatoid arthritisSeronegative

Identifiers

PMID31730497
PMCPMC6858774
OpenAlexW2986463373

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.