Cancer development based on chronic active gastritis and resulting gastric atrophy as assessed by serum levels of pepsinogen and Helicobacter pylori antibody titer

• Published in: International journal of cancer Vol. 134; no. 6; pp. 1445 - 1457
• Main Authors: Yoshida, Takeichi, Kato, Jun, Inoue, Izumi, Yoshimura, Noriko, Deguchi, Hisanobu, Mukoubayashi, Chizu, Oka, Masashi, Watanabe, Mika, Enomoto, Shotaro, Niwa, Toru, Maekita, Takao, Iguchi, Mikitaka, Tamai, Hideyuki, Utsunomiya, Hirotoshi, Yamamichi, Nobutake, Fujishiro, Mitsuhiro, Iwane, Masataka, Takeshita, Tatsuya, Ushijima, Toshikazu, Ichinose, Masao
• Format: Journal Article
• Language: English
• Published: Hoboken, NJ Wiley-Blackwell 15.03.2014; Wiley Subscription Services, Inc
• Subjects: Antibodies, Bacterial - blood; Antibodies, Bacterial - immunology; atrophic gastritis; Biological and medical sciences; Biomarkers, Tumor - blood; Biomarkers, Tumor - immunology; Cancer; cancer high‐risk; Cohort Studies; cohort study; Confidence intervals; Disease Progression; Enzyme-Linked Immunosorbent Assay; Follow-Up Studies; Gastric cancer; Gastritis, Atrophic - blood; Gastritis, Atrophic - diagnosis; Gastritis, Atrophic - etiology; Gastroenterology. Liver. Pancreas. Abdomen; Helicobacter Infections - complications; Helicobacter Infections - immunology; Helicobacter Infections - microbiology; Helicobacter pylori; Helicobacter pylori - immunology; Helicobacter pylori - pathogenicity; Humans; Infections; Inflammation - blood; Inflammation - diagnosis; Inflammation - etiology; Male; Medical research; Medical sciences; Metaplasia - blood; Metaplasia - diagnosis; Metaplasia - etiology; Middle Aged; Multiple tumors. Solid tumors. Tumors in childhood (general aspects); Other diseases. Semiology; pepsinogen; Pepsinogen A - blood; Pepsinogen C - blood; Prognosis; Radioimmunoassay; Risk Factors; Stomach - pathology; Stomach - virology; Stomach Neoplasms - blood; Stomach Neoplasms - diagnosis; Stomach Neoplasms - etiology; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; Tumors; Ulcers; High risk; Spirillaceae; Stomach cancer; Carcinogenesis; Atrophy; Cancerology; Helicobacter pylori; Cohort study; Bacteria; Serum; Gastric disease; Stomach; Spirillales; gastric cancer; Digestive system; Antibody; Atrophic gastritis; cancer high-risk; Malignant tumor; Pepsinogen; Infection; Chronic; Bacteriosis; Digestive diseases; Cancer; atrophic gastritis; cohort study; pepsinogen
• ISSN: 0020-7136; 1097-0215; 1097-0215
• DOI: 10.1002/ijc.28470

Our study investigated the relationship between gastric cancer development and activity of Helicobacter pylori‐associated chronic gastritis or the resulting chronic atrophic gastritis (CAG). A cohort of 4,655 healthy asymptomatic subjects, in whom serum pepsinogen (PG) and H. pylori antibody titer had been measured to assess the activity and stage of H. pylori‐associated chronic gastritis, was followed for up to 16 years, and cancer development was investigated. In subjects with a serologically diagnosed healthy stomach (H. pylori‐negative/CAG‐negative), cancer incidence rate was low, at 16/100,000 person‐years. With the establishment of H. pylori infection and progression of chronic gastritis, significant stepwise cancer risk elevations were seen from CAG‐free subjects (H. pylori‐positive/CAG‐negative) [hazard ratio (HR) = 8.9, 95% confidence interval (CI) = 2.7–54.7] to subjects with CAG (H. pylori‐positive/CAG‐positive) (HR = 17.7, 95% CI = 5.4–108.6) and finally to subjects with metaplastic gastritis (H. pylori‐negative/CAG‐positive) (HR = 69.7, 95% CI = 13.6–502.9). In H. pylori‐infected CAG‐free subjects, significantly elevated cancer risk was observed in the subgroup with active inflammation‐based high PG II level or potent immune response‐based high H. pylori antibody titer; the former was associated with a particularly high risk of diffuse‐type cancer, and both subgroups showed high cancer incidence rates of around 250/100,000 person‐years, comparable to that in subjects with CAG. No such risk elevation was observed in H. pylori‐infected subjects with CAG. These results clearly indicate that gastric cancer develops mainly from the gastritis‐atrophy‐metaplasia‐cancer sequence and partly from active inflammation‐based direct carcinogenesis, and that serum levels of PG and H. pylori antibody titer provide indices of cancer development in H. pylori‐infected subjects. What's new? Infection with the bacteria H. pylori is the most common risk factor for developing gastric cancer. The infection causes chronic inflammation leading to a sequence of gastritis, atrophy, metaplasia, dysplasia, cancer. This study follows up a cohort of 6,000 men after 16 years and showed that cancer risk increased with the progression of inflammation and atrophy, which can be measured by serum tests. These tests, the authors suggest, would be useful in assessing risk among people infected with H. pylori.