Evidence map›Paper›PMID 41052915›Full record

ReviewGut2025

Rise of precision medicine: can it deliver on its promise in IBD?

Stefan Schreiber, Konrad Aden, Florian Tran, Philip Rosenstiel

Abstract readReview
In one paragraph

Review in Gut, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. UBE2L6 drives ulcerative colitis progression by promoting BIRC2 degradation and activating non-canonical NF-κB signalling.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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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

4 authors.

Stefan SchreiberDepartment Internal Medicine I, Kiel University, University Hospital Schleswig Holstein, Kiel, Germany s.schreiber@mucosa.de p.rosenstiel@mucosa.de.ORCID 0000-0002-6807-9822
Konrad AdenDepartment Internal Medicine I, Kiel University, University Hospital Schleswig Holstein, Kiel, Germany.ORCID 0000-0003-3482-7316
Florian TranDepartment Internal Medicine I, Kiel University, University Hospital Schleswig Holstein, Kiel, Germany.ORCID 0000-0002-3735-9872
Philip RosenstielInstitute of Clinical Molecular Biology, Kiel University, University Hospital Schleswig Holstein, Kiel, Germany s.schreiber@mucosa.de p.rosenstiel@mucosa.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The clinical and molecular heterogeneity of IBD-both between patients and within the same individual over time-continues to pose a significant challenge to the implementation of truly personalised treatment strategies. Unlike oncology, where somatic mutation patterns define an actionable information layer, IBD lacks detectable dominant molecular drivers that can guide therapeutic choices. Although the therapeutic landscape has broadened with the advent of numerous biologics and small molecule drugs, predictive (

Indexed as

Inflammatory Bowel DiseasesPrecision MedicineBiomarkersHumansBiomarkersBIOLOGICAL THERAPYBIOMARKERSCLINICAL TRIALSCROHN'S DISEASEULCERATIVE COLITIS

Identifiers

PMID41052915
PMCPMC12703253

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.