Evidence map›Paper›PMID 41494817›Full record

ArticleBMJ open gastroenterology2026

Proton-pump inhibitor exposure and prevalence of colorectal adenoma: a retrospective analysis from the Sakkopi study.

Hannah Hofer, Sarah Wernly, Andreas Völkerer, Georg Semmler, Maria Flamm, Laurenz Hauptmann, Bernhard Wernly, Elmar Aigner, Christian Datz

Abstract read
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Article in BMJ open gastroenterology, 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Hannah HoferInternal Medicine, Saint John of God Hospital Salzburg, Salzburg, Salzburg, Austria.ORCID http://orcid.org/0009-0007-8839-0523
Sarah WernlyInternal Medicine, General Hospital Oberndorf, Teaching Hospital of the Paracelsus Medical University, Salzburg, Austria, Salzburg, Salzburg, Austria.
Andreas VölkererInternal Medicine, General Hospital Oberndorf, Teaching Hospital of the Paracelsus Medical University, Salzburg, Austria, Salzburg, Salzburg, Austria.
Georg SemmlerDivision of Gastroenterology and Hepatology, Department of Internal Medicine III, AKH Wien, Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0002-0411-166X
Maria FlammInstitute of General Practice, Paracelsus Medical University, Salzburg, Austria.
Laurenz HauptmannDivision of Cardiology, Medical University of Vienna, Vienna, Austria.
Bernhard WernlyClinic I for Internal Medicine, Salzburger Universitatsklinikum Universitatsklinik fur Innere Medizin I, Salzburg, Salzburg, Austria bernhard@wernly.net.
Elmar AignerClinic I for Internal Medicine, Salzburger Universitatsklinikum Universitatsklinik fur Innere Medizin I, Salzburg, Salzburg, Austria.
Christian DatzInternal Medicine, General Hospital Oberndorf, Oberndorf, Austria.ORCID http://orcid.org/0000-0001-7838-4532

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveProton-pump inhibitors (PPIs) are among the most widely prescribed long-term medications worldwide, yet concerns remain about their potential role in colorectal carcinogenesis. Experimental data suggest that PPI-induced hypergastrinaemia may promote colonic epithelial proliferation, but epidemiological findings are inconsistent, and colonoscopy-based evidence is limited.

methodsWe studied 4476 asymptomatic adults who underwent structured screening colonoscopy in Austria between 2007 and 2020 as part of the Sakkopi study. Regular PPI use, including dose stratification, was evaluated in this retrospective analysis in relation to adenoma prevalence, burden and anatomical distribution. Multivariable logistic regression was adjusted for age, sex, metabolic syndrome, smoking status and family history of colorectal cancer. Multinomial models examined non-advanced and advanced adenomas separately.

resultsA total of 322 (7.2%) participants reported regular PPI use. Compared with non-users, PPI users were older, had higher body mass index and more frequently fulfilled metabolic syndrome criteria. Adenomas were detected in 39% of PPI users and 33% of non-users (p=0.032). In adjusted analyses, PPI use was not associated with adenoma presence (OR 1.05; 95% CI 0.83 to 1.35), number or distribution. Dose stratification showed no gradient effect: adjusted ORs were 0.85 (0.58 to 1.26) for half-dose and 1.19 (0.83 to 1.7) for standard-dose therapy. Multinomial analyses yielded consistent null results for both non-advanced and advanced adenomas in adjusted analysis.

conclusionIn this large and well-characterised screening cohort, regular PPI therapy was not associated with colorectal adenoma prevalence, irrespective of dose or lesion characteristics.

Indexed as

AdenomaColorectal NeoplasmsProton Pump InhibitorsAdultAgedAustriaColonoscopyEarly Detection of CancerFemaleHumansMaleMiddle AgedPrevalenceRetrospective StudiesRisk FactorsProton Pump InhibitorsCOLONIC ADENOMASCOLORECTAL ADENOMASGASTRIN RECEPTORSPROTON PUMP INHIBITION

Identifiers

PMID41494817
PMCPMC12778339

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