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Antibody responses to helicobacter pylori and risk of developing colorectal cancer in a European cohort

  • Julia Butt
  • , Mazda Jenab
  • , Michael Pawlita
  • , Anne Tjønneland
  • , Cecilie Kyrø
  • , Marie Christine Boutron-Ruault
  • , Franck Carbonnel
  • , Catherine Dong
  • , Rudolf Kaaks
  • , Tilman Kuhn
  • , Heiner Boeing
  • , Matthias B. Schulze
  • , Antonia Trichopoulou
  • , Anna Karakatsani
  • , Carlo La Vecchia
  • , Domenico Palli
  • , Claudia Agnoli
  • , Rosario Tumino
  • , Carlotta Sacerdote
  • , Salvatore Panico
  • Bas Bueno-De-Mesquita, Roel Vermeulen, Inger T. Gram, Elisabete Weiderpass, Kristin Benjaminsen Borch, Jose Ramon Quiros, Antonio Agudo, Miguel Rodríguez-Barranco, Carmen Santiuste, Eva Ardanaz, Bethany van Guelpen, Sophia Harlid, Liher Imaz, Aurora Perez-Cornago, Marc J. Gunter, Semi Zouiouich, Jin Young Park, Elio Riboli, Amanda J. Cross, Alicia K. Heath, Tim Waterboer, David J. Hughes

Research output: Contribution to journalArticlepeer-review

Abstract

Background: While Helicobacter pylori (H. pylori) is the major cause of gastric cancer, it has also been suggested to be involved in colorectal cancer development. However, prospective studies addressing H. pylori and colorectal cancer are sparse and inconclusive. We assessed the association of antibody responses to H. pylori proteins with colorectal cancer in the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort. Methods: We applied H. pylori multiplex serology to measure antibody responses to 13 H. pylori proteins in prediagnostic serum samples from 485 colorectal cancer cases and 485 matched controls nested within the EPIC study. Odds ratios (OR) and 95% confidence intervals (CI) were calculated using multivariable conditional logistic regression to estimate the association of H. pylori overall and protein-specific seropositivity with odds of developing colorectal cancer. Results: Fifty-one percent of colorectal cancer cases were H. pylori seropositive compared with 44% of controls, resulting in an OR of 1.36 (95% CI, 1.00–1.85). Among the 13 individual H. pylori proteins, the association was driven mostly by seropositivity to Helicobacter cysteine-rich protein C (HcpC; OR: 1.66; 95% CI, 1.19–2.30) and Vacuolating cytotoxin A (VacA) (OR: 1.34; 95% CI, 0.99–1.82), the latter being nonstatistically significant only in the fully adjusted model. Conclusions: In this prospective multicenter European study, antibody responses to H. pylori proteins, specifically HcpC and VacA, were associated with an increased risk of developing colorectal cancer. Impact: Biological mechanisms for a potential causal role of H. pylori in colorectal carcinogenesis need to be elucidated, and subsequently whether H. pylori eradication may decrease colorectal cancer incidence.

Original languageEnglish
Pages (from-to)1475-1481
Number of pages7
JournalCancer Epidemiology Biomarkers and Prevention
Volume29
Issue number7
DOIs
Publication statusPublished - Jul 2020
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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