Evidence map›Paper›PMID 41359916›Full record

ArticleClinical and translational gastroenterology2026

Impact of Endometriosis on the Progression of Inflammatory Bowel Diseases: A Multicenter Retrospective Study.

Lucas Guillo, Oumaya El Oumami, Philippe Seksik, Guillaume Le Cosquer, Louise Méheut, Vered Abitbol, Stéphane Nancey, Anthony Buisson, Mathieu Uzzan, Mathias Vidon and 13 more

Abstract readMulticenter Study
In one paragraph

Article in Clinical and translational gastroenterology, 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

23 authors.

Lucas GuilloDepartment of Gastroenterology, University Hospital of Marseille Nord, University of Aix-Marseille, Marseille, France.ORCID 0000-0001-9024-8541
Oumaya El OumamiDepartment of Gastroenterology, Claude Huriez Hospital, University of Lille 2, CHU Lille, Lille, France.
Philippe SeksikDepartment of Gastroenterology, Centre de Recherche Saint-Antoine, Sorbonne Université, INSERM, APHP, Hôpital Saint-Antoine, Paris, France.
Guillaume Le CosquerDepartment of Gastroenterology, Toulouse University Hospital, Toulouse, France.
Louise MéheutDepartment of Gastroenterology, University Hospital of Marseille Nord, University of Aix-Marseille, Marseille, France.
Vered AbitbolDepartement of Gastroenterology, Paris Descartes University, Sorbonne Paris Cité, Cochin Hospital, APHP, Paris, France.
Stéphane NanceyDepartment of Gastroenterology, Inserm U1111-CIRI, Lyon-Sud University Hospital, Hospices Civils de Lyon, Pierre Bénite, France.
Anthony BuissonUniversité Clermont Auvergne, 3iHP, CHU Clermont-Ferrand, Service d'Hépato-Gastroentérologie, Inserm U1071, M2iSH, USC-INRA 2018, Clermont-Ferrand, France.
Mathieu UzzanDepartment of Gastroenterology, Hôpital Henri Mondor, APHP, Créteil, France.
Mathias VidonDepartment of Gastroenterology, Georges Pompidou European Hospital, APHP, Paris Sorbonnes University, Paris, France.
Ludovic CailloDepartment of Gastroenterology, University Hospital of Nimes, Nimes, France.
Bénédicte CaronDepartment of Gastroenterology and Inserm NGERE U1256, University Hospital of Nancy, University of Lorraine, Vandoeuvre-lès-Nancy, France.
Alban BenezechDepartement of Gastroenterology, Henri Duffaut Hospital, Avignon, France.
Calina AtanasiuDepartment of Gastroenterology, Hôpital Saint-Joseph, Paris, France.
Nicolas RichardDepartment of Gastroenterology, Rouen University Hospital, Rouen, France.
Alexandre NuzzoDepartment of Gastroenterology, IBD and Intestinal Failure, AP-HP Hôpital Beaujon, Clichy, France.
Catherine Le BerreDepartment of Gastroenterology, Institut des Maladies de l'Appareil Digestif (IMAD), CIC Inserm 1413, Nantes University Hospital, Nantes, France.
Anne BourrierDepartment of Gastroenterology, Centre de Recherche Saint-Antoine, Sorbonne Université, INSERM, APHP, Hôpital Saint-Antoine, Paris, France.
Catherine ReenaersDepartment of Gastroenterology, CHU Liège, Sart Tilman, Liège, Belgium.
Julien LabreucheULR 2694-METRICS, CHU Lille, Lille, Hauts-de-France, France.
Mélanie SerreroDepartment of Gastroenterology, University Hospital of Marseille Nord, University of Aix-Marseille, Marseille, France.
Chrystèle RubodDepartment of Gynecology and Obstetrics, CHU Lille, F-59000 Lille, France.
Pauline WilsDepartment of Gastroenterology, Claude Huriez Hospital, University of Lille 2, CHU Lille, Lille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWomen with endometriosis have a higher risk of developing inflammatory bowel diseases (IBDs). This study aimed to better understanding the impact of endometriosis on the course of IBD.

methodsWe conducted a retrospective cohort study in 18 French and Belgian IBD centers between June 2022 and March 2023. Any patient with both conditions was eligible for inclusion. They were randomly matched to 1 or 2 patients with IBD without endometriosis. The impact on IBD progression was assessed using a composite severity criterion including intestinal damage or need for bowel surgery.

resultsOverall, 207 patients with both conditions (149 Crohn's disease [CD]; 58 ulcerative colitis [UC]) were matched to 409 patients with IBD alone. The median follow-up duration for IBD was 10 years (5.75-17). No difference was observed between the 2 groups regarding CD location, disease phenotype, and anoperineal involvement. Proctitis were more frequent in patients with UC and endometriosis. Patients with IBD with endometriosis were significantly less exposed to immunosuppressants (UC P < 0.01; CD P < 0.001) and biologics (UC P < 0.01; CD P < 0.001). Patients with CD with endometriosis had a less severe disease course compared with patients without endometriosis (hazard ratio 0.68, 95% confidence interval 0.50-0.92, P = 0.011). Patients with UC with endometriosis had not a significant different disease course compared with patients without endometriosis (hazard ratio 1.73, 95% confidence interval 0.74-4.00, P = 0.20). These results were similar in the subgroup of patients with endometriosis treated surgically. DISCUSSION: Endometriosis does not negatively influence the course of IBD, patients with CD even have a less severe progression. Patients were significantly less exposed to immunosuppressants and biologics.

Indexed as

Colitis, UlcerativeCrohn DiseaseEndometriosisAdultBelgiumBiological ProductsDisease ProgressionFemaleFollow-Up StudiesFranceHumansImmunosuppressive AgentsMiddle AgedRetrospective StudiesSeverity of Illness IndexBiological ProductsImmunosuppressive AgentsCrohn's diseasedisease courseendometriosisinflammatory bowel diseaseulcerative colitis

Identifiers

PMID41359916
PMCPMC12922932

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