# Genetic Susceptibility to Helicobacter pylori Infection and Pancreatic Cancer Risk: A Two-Sample Mendelian Randomisation Study

**Authors:** Nien-Yu Yang, Te-Min Ke, Yicong Huang, Artitaya Lophatananon, Kenneth R. Muir

PMC · DOI: 10.3390/life16020284 · 2026-02-07

## TL;DR

This study used genetic data to investigate whether Helicobacter pylori infection causes pancreatic cancer, finding no significant link.

## Contribution

The study applies two-sample Mendelian randomisation to assess a potential causal relationship between H. pylori and pancreatic cancer.

## Key findings

- No significant causal association was found between H. pylori infection and pancreatic cancer risk.
- Multiple MR methods confirmed null results with no strong evidence of pleiotropy.
- Results suggest the need for larger studies with refined exposure measures.

## Abstract

Background/Objectives: Pancreatic cancer is one of the most lethal malignancies, with poor survival and few established modifiable risk factors. While Helicobacter pylori (H. pylori) infection is a known cause of gastric cancer, its role in pancreatic cancer remains unclear, with inconsistent observational evidence. Methods: We applied two-sample Mendelian randomisation (2SMR) to assess the causal effect of H. pylori infection on pancreatic cancer risk. Genetic instruments were derived from GWAS data on anti-H. pylori IgG levels in the ALSPAC cohort (n = 4638). Outcomes were pancreatic cancer cases from UK Biobank (936 cases, 400,294 controls) and a combined dataset including UK Biobank, FinnGen, and MVP (5979 cases, 1,234,860 controls). Inverse-variance weighted (IVW) MR was the primary method, supported by MR-Egger, weighted median/mode and MR-PRESSO, with sensitivity analyses for pleiotropy. Results: No significant causal association was observed. IVW ORs were 1.039 (95% CI: 0.846–1.440, p = 0.466) for UK Biobank and 1.077 (95% CI: 0.962–1.206, p = 0.197) for the combined dataset. All complementary methods yielded null results, with no strong evidence of pleiotropy. Conclusions: This 2SMR study found no evidence that H. pylori infection causally increases pancreatic cancer risk. Larger studies with refined exposure measures are warranted.

## Linked entities

- **Diseases:** pancreatic cancer (MONDO:0005192), gastric cancer (MONDO:0001056)

## Full-text entities

- **Genes:** VacA [NCBI Gene 48201093], CagA [NCBI Gene 48200769]
- **Diseases:** obesity (MESH:D009765), extra-gastric cancers (MESH:D013274), inflammatory (MESH:D007249), injury to (MESH:D014947), H. pylori (MESH:D016481), MVP (OMIM:157700), Malignant neoplasm of pancreas (MESH:D010190), cancer (MESH:D009369), diabetes (MESH:D003920), infection (MESH:D007239), chronic pancreatitis (MESH:D050500)
- **Species:** Helicobacter pylori (species) [taxon 210], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs117912702

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941709/full.md

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Source: https://tomesphere.com/paper/PMC12941709