Evidence map›Paper›PMID 25146552›Full record

SynthesisEndocrine2015

Incretin-based therapies and acute pancreatitis risk: a systematic review and meta-analysis of observational studies.

Carlo B Giorda, Carlotta Sacerdote, Elisa Nada, Lisa Marafetti, Ileana Baldi, Roberto Gnavi

Abstract readMeta-AnalysisSystematic Review
PubMed Publisher
In one paragraph

Synthesis in Endocrine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 3% of its field
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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

  1. Pooled it
  2. Acute pancreatitis following semaglutide therapy: a case report.Annals of medicine and surgery (2012) · 2026
    Article
  3. Article
  4. Article
  5. Dose-dependent pancreatitis risk associated with GLP-1 agonists.Journal of diabetes and metabolic disorders · 2025
    Article
  6. Article
  7. Article
  8. Glucagon-Like Peptide-1 Receptor Agonist Cases Reported to United States Poison Centers, 2017-2022.Journal of medical toxicology : official journal of the American College of Medical Toxicology · 2024
    Article
  9. Article
  10. Article
  11. Diabetes following acute pancreatitis.The lancet. Gastroenterology & hepatology · 2021
    Review
  12. Role of Glucagon-Like Peptide-1 (GLP-1) Receptor Agonists in Hypoglycemia.Clinical medicine insights. Endocrinology and diabetes · 2021
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. DPP-4 Inhibition and the Path to Clinical Proof.Frontiers in endocrinology · 2019
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 1 country.

Carlo B GiordaMetabolism and Diabetes Unit, ASL TO5, Regione Piemonte, Chieri, Italy, giordaca@tin.it.
Carlotta Sacerdote
Elisa Nada
Lisa Marafetti
Ileana Baldi
Roberto Gnavi
Regione PiemonteMedica (Italy) · ITUniversity of Padua · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Concerns raised by several animal studies, case reports, and pharmacovigilance warnings over incretin-based therapy potentially exposing type two diabetes patients to an elevated risk of pancreatitis have cast a shadow on the overall safety of this class of drugs. This systematic review evaluates the data from observational studies that compared treatment with or without incretins and the risk of pancreatitis. We searched PubMed for publications with the key terms incretins or GLP-1 receptor agonists or DPP-4 inhibitors or sitagliptin or vildagliptin or saxagliptin or linagliptin or alogliptin or exenatide or liraglutide AND pancreatitis in the title or abstract. Studies were evaluated against the following criteria: design (either cohort or case-control); outcome definition (incidence of pancreatitis); exposure definition (new or current or past incretins users); and comparison between patients receiving incretins or not for type 2 diabetes. Two authors independently selected the studies and extracted the data. Six studies meeting the inclusion criteria were reviewed. No difference was found in the overall risk of pancreatitis between incretin users and non-users (odds ratio 1.08; 95 % CI [0.84-1.40]). A risk increase lower than 35 % cannot be excluded according to the power calculation. This systematic review and meta-analysis suggests that type 2 diabetes patients receiving incretin-based therapy are not exposed to an elevated risk of pancreatitis. Limitations of this analysis are the low prevalence of incretin users and the lack of a clear distinction by the studies between therapy with DPP-4 inhibitors or with GLP-1 receptor agonists.

Indexed as

Observational Studies as TopicDiabetes Mellitus, Type 2HumansIncretinsPancreatitisIncretins

Identifiers

PMID25146552
OpenAlexW2058206834

What Socratic holds

Textmetadata
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.