Evidence map›Paper›PMID 39639588›Full record

ArticleCancer2025

A genome-wide association study identifies eight loci associated with intraductal papillary mucinous neoplasm progression toward malignancy.

Manuel Gentiluomo, Chiara Corradi, Laura Apadula, Annalisa Comandatore, Gaetano Lauri, Gemma Rossi, Giulia Peduzzi, Stefano Crippa, Cosmeri Rizzato, Massimo Falconi and 4 more

Abstract read
In one paragraph

Article in Cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

14 authors.

Manuel GentiluomoDepartment of Biology, University of Pisa, Pisa, Italy.ORCID https://orcid.org/0000-0002-0366-9653
Chiara CorradiDepartment of Biology, University of Pisa, Pisa, Italy.
Laura ApadulaPancreato-Biliary Endoscopy and Endosonography Division, Pancreas Translational and Clinical Research Center, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Annalisa ComandatoreGeneral Surgery Unit, Cisanello Hospital, Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.
Gaetano LauriPancreato-Biliary Endoscopy and Endosonography Division, Pancreas Translational and Clinical Research Center, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Gemma RossiPancreato-Biliary Endoscopy and Endosonography Division, Pancreas Translational and Clinical Research Center, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Giulia PeduzziDepartment of Biology, University of Pisa, Pisa, Italy.
Stefano CrippaVita-Salute San Raffaele University, Milan, Italy.
Cosmeri RizzatoDepartment of Biology, University of Pisa, Pisa, Italy.
Massimo FalconiVita-Salute San Raffaele University, Milan, Italy.
Paolo Giorgio ArcidiaconoPancreato-Biliary Endoscopy and Endosonography Division, Pancreas Translational and Clinical Research Center, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Luca MorelliGeneral Surgery Unit, Cisanello Hospital, Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.
Gabriele CapursoPancreato-Biliary Endoscopy and Endosonography Division, Pancreas Translational and Clinical Research Center, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Daniele CampaDepartment of Biology, University of Pisa, Pisa, Italy.ORCID https://orcid.org/0000-0003-3220-9944

Funding

Associazione Italiana per la Ricerca sul Cancro IG 2019-ID 23672Associazione Italiana per la Ricerca sul Cancro IG 2021 ID 26201
6 · The paper itself

Abstract

backgroundIntraductal papillary mucinous neoplasms (IPMNs) are precursors to pancreatic cancer, but not all IPMNs progress to cancer. The objective of this study was to identify the germline genetic variants associated with IPMN clinical progression by conducting the first genome-wide association study (GWAS) and computing a polygenic hazard score (PHS) in 338 patients with IPMN.

methodsThe study population was divided into two subsets, and a Cox analysis adjusted for sex, age, cyst size at diagnosis, and the top 10 principal components was performed. A PHS was calculated using the genotypes of common variants associated with IPMN progression identified.

resultsEight loci with significant associations (p < 5 × 10

conclusionsThe current results study advance the understanding of individual predisposition to IPMN progression and underscore the potential use of genetics in the stratification of patients who have IPMN.

Indexed as

Disease ProgressionGenome-Wide Association StudyPancreatic NeoplasmsAdenocarcinoma, MucinousAgedCarcinoma, Pancreatic DuctalFemaleGenetic Predisposition to DiseaseGenotypeHumansMaleMiddle AgedPancreatic Intraductal NeoplasmsPolymorphism, Single Nucleotidegenome‐wide association study (GWAS)intraductal papillary mucinous neoplasmspancreatic cancerpolygenic scoreprogression

Identifiers

PMID39639588
PMCPMC11694541

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Registered trials

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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.