Evidence map›Paper›PMID 42586604›Full record

ArticleJournal of Crohn's & colitis2026

Longitudinal transcriptomic analysis of mucosa in ulcerative colitis after anti-tumor necrosis factor withdrawal compared to continued treatment.

Emma Rapp, Ingrid Prytz Berset, Sinan U Umu, Espen Sønderaal Bækkevold, Karen Sivertsen Utheim, Alexander Dietrich, Markus List, Kjersti Thorvaldsen Hagen, Frode Lerang, Dag Arne Lihaug Hoff and 3 more

Abstract read
In one paragraph

Article in Journal of Crohn's & colitis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

13 authors.

Emma RappDepartment of Pathology, Oslo University Hospital, 0372 Oslo, Norway.ORCID 0009-0007-4980-7066
Ingrid Prytz BersetDepartment of Gastroenterology, Møre & Romsdal Hospital Trust, 6017 Ålesund, Norway.ORCID 0000-0002-2014-8497
Sinan U UmuDepartment of Pathology, Oslo University Hospital, 0372 Oslo, Norway.ORCID 0000-0001-8081-7819
Espen Sønderaal BækkevoldDepartment of Pathology, Oslo University Hospital, 0372 Oslo, Norway.
Karen Sivertsen UtheimInstitute of Clinical Medicine, University of Oslo, 0450 Oslo, Norway.
Alexander DietrichData Science in Systems Biology, TUM School of Life Sciences, Technical University of Munich, 85354 Freising, Germany.ORCID 0000-0002-8661-0453
Markus ListData Science in Systems Biology, TUM School of Life Sciences, Technical University of Munich, 85354 Freising, Germany.ORCID 0000-0002-0941-4168
Kjersti Thorvaldsen HagenInstitute of Clinical Medicine, University of Oslo, 0450 Oslo, Norway.
Frode LerangDepartment of Gastroenterology, Østfold Hospital Trust, 1714 Grålum, Sarpsborg, Norway.ORCID 0000-0003-2243-8882
Dag Arne Lihaug HoffDepartment of Gastroenterology, Møre & Romsdal Hospital Trust, 6017 Ålesund, Norway.ORCID 0000-0002-7861-2125
Knut E A LundinInstitute of Clinical Medicine, University of Oslo, 0450 Oslo, Norway.
Frode Lars JahnsenDepartment of Pathology, Oslo University Hospital, 0372 Oslo, Norway.
Diana DomanskaDepartment of Pathology, Oslo University Hospital, 0372 Oslo, Norway.

Funding

South-Eastern Norway Regional Health Authority 2023090
6 · The paper itself

Abstract

BACKGROUND AND

aimsMonoclonal antibodies against tumor necrosis factor (anti-TNF) are effective agents in the treatment of moderate-to-severe ulcerative colitis (UC). It is unclear whether such treatment can safely be discontinued without relapse. This study aimed to identify biomarkers to predict which patients can successfully stop anti-TNF treatment, and to increase our understanding of the pathogenesis of relapse after withdrawal and flare on continued therapy.

methodsWe analyzed longitudinal bulk RNA-sequencing data derived from rectal mucosal biopsies from 163 patients in the BIOSTOP study collected at baseline, after 2 years (end of study), and at flares or relapse points.

resultsIn this cohort, pre-withdrawal transcriptomic profiles did not distinguish patients who later relapsed from those who remained in long-term remission. Longitudinal analysis of patients who relapsed or flared were both characterized by inflammatory gene expression profiles (eg, CXCL9, CXCL10, OSMR, SELE) and changes in cell-type composition typical for active UC (eg, monocytes/macrophages and THY1+ FAP+ PDPN+ activated fibroblasts). Both groups showed enrichment of T-cell-associated transcriptional signatures, including CD8 T-cell-related genes and IL-17-associated pathways. Additionally, both patient groups showed increased expression of targets of alternative therapeutic agents, suggesting potential treatment options for specific patient subgroups.

conclusionsOur findings provide insights into the inflammatory mechanisms driving relapse after anti-TNF withdrawal and flare on continued treatment. The dataset offers a valuable resource for future research to improve personalized treatment strategies in UC.

Indexed as

Colitis, UlcerativeIntestinal MucosaTumor Necrosis Factor-alphaAdultBiomarkersFemaleGene Expression ProfilingHumansInfliximabLongitudinal StudiesMaleMiddle AgedRecurrenceTranscriptomeTreatment InterruptionBiomarkersInfliximabTumor Necrosis Factor-alphaanti-TNF withdrawalgene expressionulcerative colitis

Identifiers

PMID42586604
PMCPMC13467011

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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.