Evidence map›Paper›PMID 37914180›Full record

ArticleRMD open2023

Distinction and prognosis of early arthritis phenotypes: an analysis in three European cohorts.

Alexandre Sepriano, Bastiaan van Dijk, Sofia Ramiro, Annette van der Helm-van Mil, Bernard Combe, Dirkjan van Schaardenburg, Maarten de Wit, Alison Kent, Elsa Mateus, Robert Landewé

Open access · goldAbstract read
In one paragraph

Article in RMD open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. 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

10 authors at 5 institutions in 4 countries.

Alexandre SeprianoNOVA Medical School, Universidade Nova de Lisboa, Lisboa, Portugal alexsepriano@gmail.com.ORCID 0000-0003-1954-0229
Bastiaan van DijkRheumatology, Leiden University Medical Center, Leiden, Netherlands.
Sofia RamiroRheumatology, Leiden University Medical Center, Leiden, Netherlands.ORCID 0000-0002-8899-9087
Annette van der Helm-van MilRheumatology, Leiden University Medical Center, Leiden, Netherlands.ORCID 0000-0001-8572-1437
Bernard CombeUniversity of Montpellier, Montpellier, France.ORCID 0000-0003-4002-1861
Dirkjan van SchaardenburgRheumatology, Reade and Amsterdam University Medical Center, Amsterdam, Netherlands.ORCID 0000-0003-4006-3762
Maarten de WitEULAR Patient Research Partner Network, Zurich, Switzerland.ORCID 0000-0002-8428-6354
Alison KentEULAR Patient Research Partner Network, Zurich, Switzerland.
Elsa MateusEULAR Patient Research Partner Network, Zurich, Switzerland.
Robert LandewéAmsterdam Rheumatology Center, AMC, Amsterdam, Netherlands.ORCID 0000-0002-0577-6620
Leiden University Medical Center · NLThe Geneva Association · CHReade · NLUniversité de Montpellier · FRZuyderland Medisch Centrum · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe objective of this study is to evaluate whether there are differences in the long-term prognosis across various phenotypes of early arthritis (EA).

methodsThree EA cohorts (Reade, Etude et Suivi des Polyarthrites Indifférenciées Récentes (ESPOIR) and Early Arthritis Clinic (EAC)) were analysed. Clinical data were collected up to 24 years. Hands and feet radiographs were scored according to the Sharp van der Heijde (SvdH) method. Latent class analysis was applied to determine the EA phenotypes at baseline. Each class received a label reflecting its most prominent features. Prognostic outcomes included Health Assessment Questionnaire (HAQ), Short Form 36 (SF36) and SvdH score. The association between class membership and outcomes over time was tested in multivariable models.

resultsIn total, 390 (Reade), 798 (ESPOIR) and 3991 (EAC) patients were analysed separately. Two classes with symmetrical polyarthritis emerged; one of these labelled as autoimmune inflammatory polyarthritis (AIPA), had high likelihood of acute phase reactants (APR) elevation and autoantibody positivity, while the other (mild-inflammatory polyarthritis; MIPA) had not. A third class had oligoarthritis of upper limbs (OAUL) and could be subdivided into autoimmune OAUL and mild-inflammatory OAUL. A fifth class had oligoarthritis of lower limbs. The SvdH scores were worse in patients with APR/autoantibodies (AIPA) than in those without (MIPA). No clinically meaningful differences across classes in HAQ or SF36 over time were found.

conclusionRadiographic progression over time primarily occurs in EA patients with APR/autoantibodies. The absence of these markers, however, does not necessarily translate into better long-term function and quality of life. Clinicians should not only aim at preventing joint damage, but look beyond structural progression in order to further improve the lives of people with EA.

Indexed as

Arthritis, RheumatoidAutoantibodiesDisease ProgressionHumansPhenotypePrognosisQuality of LifeAutoantibodiesArthritis, RheumatoidMagnetic Resonance ImagingOutcome and Process Assessment, Health Care

Identifiers

PMID37914180
PMCPMC10626756
OpenAlexW4388126419

What OpenQuestion holds

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LicenceCC BY-NC
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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.