Evidence map›Paper›PMID 42370112›Full record

ArticleEULAR rheumatology open2026

Spondyloarthritis and inflammatory bowel disease: towards a more severe and refractory disease phenotype.

Juliane Michel, Clément Prati, Lucine Vuitton, Charline Vauchy, Eric Toussirot, Frederic Mauny, Marc Puyraveau, Mickaël Chouk, Olivier Fakih, Daniel Wendling and 1 more

Abstract read
In one paragraph

Article in EULAR rheumatology open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Juliane MichelUniversité Marie et Louis Pasteur, Service de Rhumatologie, CHU de Besançon, 25000 Besançon, France.
Clément PratiUniversité Marie et Louis Pasteur, Service de Rhumatologie, CHU de Besançon, 25000 Besançon, France.
Lucine VuittonUniversité Marie et Louis Pasteur, UFR Santé, UMR1098, EFS, INSERM, Besançon, France.
Charline VauchyUniversité Marie et Louis Pasteur, Centre investigation clinique INSERM CIC-1431, CHU de Besançon, 25000 Besançon, France.
Eric ToussirotUniversité Marie et Louis Pasteur, Centre investigation clinique INSERM CIC-1431, CHU de Besançon, 25000 Besançon, France.
Frederic MaunyUniversité Marie et Louis Pasteur, Centre investigation clinique INSERM CIC-1431, CHU de Besançon, 25000 Besançon, France.
Marc PuyraveauUniversité Marie et Louis Pasteur, Centre investigation clinique INSERM CIC-1431, CHU de Besançon, 25000 Besançon, France.
Mickaël ChoukUniversité Marie et Louis Pasteur, Service de Rhumatologie, CHU de Besançon, 25000 Besançon, France.
Olivier FakihUniversité Marie et Louis Pasteur, Service de Rhumatologie, CHU de Besançon, 25000 Besançon, France.
Daniel WendlingUniversité Marie et Louis Pasteur, Service de Rhumatologie, CHU de Besançon, 25000 Besançon, France.
Frank VerhoevenUniversité Marie et Louis Pasteur, Service de Rhumatologie, CHU de Besançon, 25000 Besançon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: The coexistence of inflammatory bowel disease (IBD) and spondyloarthritis (SpA) poses significant diagnostic and therapeutic challenges. This study aimed to compare clinical characteristics and treatment profiles of patients with both SpA and IBD (SpA/IBD) to those with SpA or IBD alone. Methods: We performed a single-centre observational study including 62 consecutive patients with SpA/IBD followed between 2019 and 2022. Patients met Assessment of SpondyloArthritis International Society 2009 criteria for SpA and had confirmed IBD. Demographics, clinical features, imaging, and biologic disease-modifying antirheumatic drug (bDMARD) usage were collected. For comparison, we included 100 patients with a single diagnosis of SpA or IBD, representing the Maladies Inflammatoires SysTémIques Chroniques cohort enrolled over the same period. Results: Among patients with SpA/IBD (51% male, 67% HLA-B27+), IBD was more often diagnosed first. Compared with SpA alone, patients with SpA/IBD had more psoriasis (27% vs 17%, Conclusions: Patients with SpA/IBD exhibit more severe disease and therapeutic challenges, highlighting the need for tailored management and consideration of earlier combination biologic therapies.

Identifiers

PMID42370112
PMCPMC13292410

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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.