학술논문

“True” Helicobacter pylori infection and non‐cardia gastric cancer: A pooled analysis within the Stomach Cancer Pooling (StoP) Project
Document Type
article
Source
Helicobacter. 27(3)
Subject
Epidemiology
Biomedical and Clinical Sciences
Health Sciences
Clinical Research
Emerging Infectious Diseases
Cancer
Digestive Diseases - (Peptic Ulcer)
Infectious Diseases
Prevention
Digestive Diseases
4.1 Discovery and preclinical testing of markers and technologies
Detection
screening and diagnosis
Case-Control Studies
Helicobacter Infections
Helicobacter pylori
Humans
Prospective Studies
Risk Factors
Stomach Neoplasms
Helicobacter pylori
Consortium
pooled analysis
stomach neoplasms
Biological Sciences
Medical and Health Sciences
Gastroenterology & Hepatology
Biological sciences
Biomedical and clinical sciences
Health sciences
Language
Abstract
BackgroundHelicobacter 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.MethodsA 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.ResultsThe 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.ConclusionThe 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.