Evidence map›Paper›PMID 40735319›Full record

ReviewFrontiers in immunology2025

GLP-1 receptor agonists in IBD: exploring the crossroads of metabolism and inflammation.

Giulia Migliorisi, Roberto Gabbiadini, Arianna Dal Buono, Matteo Ferraris, Giuseppe Privitera, Lorenzo Petronio, Peter Bertoli, Cristina Bezzio, Alessandro Armuzzi

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
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

9 authors.

Giulia MigliorisiIBD Center, Humanitas Research Hospital - IRCCS, Rozzano, Milan, Italy.
Roberto GabbiadiniIBD Center, Humanitas Research Hospital - IRCCS, Rozzano, Milan, Italy.
Arianna Dal BuonoIBD Center, Humanitas Research Hospital - IRCCS, Rozzano, Milan, Italy.
Matteo FerrarisIBD Center, Humanitas Research Hospital - IRCCS, Rozzano, Milan, Italy.
Giuseppe PriviteraIBD Center, Humanitas Research Hospital - IRCCS, Rozzano, Milan, Italy.
Lorenzo PetronioIBD Center, Humanitas Research Hospital - IRCCS, Rozzano, Milan, Italy.
Peter BertoliIBD Center, Humanitas Research Hospital - IRCCS, Rozzano, Milan, Italy.
Cristina BezzioIBD Center, Humanitas Research Hospital - IRCCS, Rozzano, Milan, Italy.
Alessandro ArmuzziIBD Center, Humanitas Research Hospital - IRCCS, Rozzano, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) represent a cornerstone in the treatment of diabetes and obesity and have emerged as a promising option for other metabolic disorders, including hepatic steatosis. Recent evidence highlights the direct and indirect anti-inflammatory properties of GLP-1, suggesting a potential additional therapeutic strategy for patients with inflammatory bowel disease (IBD). However, side effects of GLP-1 RAs, particularly those affecting the gastrointestinal system, may limit their use in patients with IBD. The rising prevalence of IBD worldwide and the ageing of the IBD population will likely increase the number of patients with metabolic comorbidities who may potentially benefit from a combination treatment with GLP-1 RAs. A profound comprehension of the physiological function of intestinal homeostasis and permeability is essential to more accurately evaluate the prospective application of GLP-1 RAs in patients with ongoing inflammation. While preclinical studies support this hypothesis, robust clinical evidence remains limited. This narrative review aims to provide a synthesis of current knowledge regarding the anti-inflammatory properties of GLP-1, with a particular focus on safety concerns and potential future directions for its use in IBD management.

Indexed as

Anti-Inflammatory AgentsGlucagon-Like Peptide-1 Receptor AgonistsInflammatory Bowel DiseasesAnimalsGlucagon-Like Peptide 1Glucagon-Like Peptide-1 ReceptorHumansInflammationAnti-Inflammatory AgentsGlucagon-Like Peptide 1Glucagon-Like Peptide-1 ReceptorGlucagon-Like Peptide-1 Receptor AgonistsdiabetesGLP-1GLP-1 receptor agonistsIBDobesity

Identifiers

PMID40735319
PMCPMC12306662

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.