Mechanisms for the Sex-Specific Effect of H. Pylori on Risk of Gastroesophageal Reflux Disease and Barrett's Esophagus

Author:

Wang Sabrina E.12ORCID,Dashti S. Ghazaleh34ORCID,Hodge Allison M.12ORCID,Dixon-Suen Suzanne C.25ORCID,Castaño-Rodríguez Natalia6ORCID,Thomas Robert J.S.7ORCID,Giles Graham G.128ORCID,Milne Roger L.128ORCID,Boussioutas Alex910ORCID,Kendall Bradley J.1112ORCID,English Dallas R.12ORCID

Affiliation:

1. 1Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Victoria, Australia.

2. 2Cancer Epidemiology Division, Cancer Council Victoria, Melbourne, Victoria, Australia.

3. 3Clinical Epidemiology and Biostatistics Unit, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.

4. 4Department of Pediatrics, University of Melbourne, Melbourne, Victoria, Australia.

5. 5Institute for Physical Activity and Nutrition, Deakin University, Geelong, Victoria, Australia.

6. 6School of Biotechnology and Biomolecular Sciences, University of New South Wales, Kensington, New South Wales, Australia.

7. 7Department of Medicine, Royal Melbourne Hospital, Melbourne, Victoria, Australia.

8. 8Department of Precision Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, Victoria, Australia.

9. 9Department of Gastroenterology, The Alfred, Melbourne, Victoria, Australia.

10. 10Central Clinical School, Monash University, Melbourne, Victoria, Australia.

11. 11Department of Medicine, The University of Queensland, Brisbane, Queensland, Australia.

12. 12Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Queensland, Australia.

Abstract

Abstract Background: Mechanisms for how Helicobacter pylori infection affects risk of gastroesophageal reflux disease (GERD) and Barrett's esophagus are incompletely understood and might differ by sex. Methods: In a case–control study nested in the Melbourne Collaborative Cohort Study with 425 GERD cases and 169 Barrett's esophagus cases (identified at 2007–2010 follow-up), we estimated sex-specific odds ratios for participants who were H. pylori seronegative versus seropositive at baseline (1990–1994). To explore possible mechanisms, we (i) compared patterns of H. pylori-induced gastritis by sex using serum pepsinogen-I and gastrin-17 data and (ii) quantified the effect of H. pylori seronegativity on Barrett's esophagus mediated by GERD using causal mediation analysis. Results: For men, H. pylori seronegativity was associated with 1.69-fold [95% confidence interval (CI), 1.03–2.75] and 2.28-fold (95% CI, 1.27–4.12) higher odds of GERD and Barrett's esophagus, respectively. No association was observed for women. H. pylori-induced atrophic antral gastritis was more common in men (68%) than in women (56%; P = 0.015). For men, 5 of the 15 per 1,000 excess Barrett's esophagus risk from being seronegative were mediated by GERD. Conclusions: Men, but not women, who were H. pylori seronegative had increased risks of GERD and Barrett's esophagus. A possible explanation might be sex differences in patterns of H. pylori-induced atrophic antral gastritis, which could lead to less erosive reflux for men. Evidence of GERD mediating the effect of H. pylori on Barrett's esophagus risk among men supports this proposed mechanism. Impact: The findings highlight the importance of investigating sex differences in the effect of H. pylori on risk of GERD and Barrett's esophagus in future studies.

Funder

Australian National Health and Medical Research Council

Cancer Council Victoria

Victorian Cancer Registry

NHMRC project

Cancer Institute NSW Early Career Fellowship

Publisher

American Association for Cancer Research (AACR)

Subject

Oncology,Epidemiology

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