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“True” Helicobacter pylori infection and non-cardia gastric cancer: A pooled analysis within the Stomach Cancer Pooling (StoP) Project

  • Samantha Morais
  • , Adriana Costa
  • , Gabriela Albuquerque
  • , Natália Araújo
  • , Shoichiro Tsugane
  • , Akihisa Hidaka
  • , Gerson Shigueaki Hamada
  • , Weimin Ye
  • , Amelie Plymoth
  • , Marcis Leja
  • , Evita Gasenko
  • , David Zaridze
  • , Dmitry Maximovich
  • , Reza Malekzadeh
  • , Mohammad H. Derakhshan
  • , Claudio Pelucchi
  • , Eva Negri
  • , M. Constanza Camargo
  • , Maria Paula Curado
  • , Jesus Vioque
  • Zuo Feng Zhang, Carlo La Vecchia, Paolo Boffetta, Nuno Lunet
  • University of Porto
  • Laboratório para a Investigação Integrativa e Translacional em Saúde Populacional (ITR)
  • National Cancer Center Japan
  • National Institutes of Biomedical Innovation, Health and Nutrition
  • Nikkei Disease Prevention Center
  • Karolinska Institutet
  • Digestive Diseases Centre GASTRO
  • University of Latvia
  • Riga East University Hospital
  • Blokhin Cancer Research Center
  • Tehran University of Medical Sciences
  • University of Glasgow
  • University of Milan
  • Pegaso Telematic University
  • National Institutes of Health
  • A.C.Camargo Cancer Center
  • Instituto de Investigación Sanitaria y Biomédica de Alicante
  • CIBER Epidemiología y Salud Pública (CIBERESP)
  • University of California at Los Angeles

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

Background: Helicobacter pylori is the most important risk factor for non-cardia gastric cancer (NCGC); however, the magnitude of the association varies across epidemiological studies. This study aimed to quantify the association between H. pylori infection and NCGC, using different criteria to define infection status. Methods: A pooled analysis of individual-level H. pylori serology data from eight international studies (1325 NCGC and 3121 controls) from the Stomach Cancer Pooling (StoP) Consortium was performed. Cases and controls with a negative H. pylori infection status were reclassified as positive considering the presence of anti-Cag A antibodies, gastric atrophy, or advanced stage at diagnosis, as available and applicable. A two-stage approach was used to pool study-specific adjusted odds ratios (OR), and 95% confidence intervals (95% CI). A meta-analysis of published prospective studies assessing H. pylori seropositivity in NCGCs was conducted. Results: The OR for the association between serology-defined H. pylori and NCGC was 1.45 (95% CI: 0.87–2.42), which increased to 4.79 (95% CI: 2.39–9.60) following the reclassification of negative H. pylori infection. The results were consistent across strata of sociodemographic characteristics, clinical features and lifestyle factors, though significant differences were observed according to geographic region—a stronger association in Asian studies. The pooled risk estimates from the literature were 3.01 (95% CI: 2.22–4.07) for ELISA or EIA and 9.22 (95% CI: 3.12–27.21) for immunoblot or multiplex serology. Conclusion: The NCGC risk estimate from StoP based on the reclassification of H. pylori seronegative individuals is consistent with the risk estimates obtained from the literature. Our classification algorithm may be useful for future studies.

Original languageEnglish
Article numbere12883
JournalHelicobacter
Volume27
Issue number3
DOIs
StatePublished - Jun 2022

Keywords

  • Consortium
  • Helicobacter pylori
  • pooled analysis
  • stomach neoplasms

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