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Ethnic difference in serology of Helicobacter pylori CagA between Japanese and non-Japanese Brazilians for non-cardia gastric cancer
Authors:Tatemichi Masayuki  Hamada Gerson Shigeaki  Nishimoto Inês Nobuko  Kowalski Luiz Paulo  Iriya Kiyoshi  Rodrigues Joaquim Josê Gama  Tsugane Shoichiro
Affiliation:Epidemiology and Biostatistics Division, National Cancer Center Research Institute East, 6–5–1 Kashiwanoha, Kashiwa, Chiba 277–8577;Department of Environmental and Occupational Health, Toho University School of Medicine, 6–21–15 Omorinishi, Ota-ku, Tokyo 143–8540;Nikkei Disease Prevention Center, Santa Cruz Hospital Research Center, Rua Santa Cruz 398, São Paulo, SP, 04122–000, Brazil;Research Center;Department of Head and Neck Surgery, A. C. Camargo Hospital, Rua Prof. Antonio Prudente 211, São Paulo, SP, 01509–900, Brazil;Department of Pathology;Department of Gastroenterology, School of Medicine, University of São Paulo, Av. Dr. Arnaldo 455, São Paulo, SP, 01246–904, Brazil
Abstract:The usefulness of serology against CagA of Helicobacter pylori as a biomarker to identify high-risk individuals for non-cardia gastric cancer (ncGC) remains unclear among several ethnic populations with a high prevalence of cagA-positive strains. We investigated ethnic differences of CagA serology in two sets of case-control subjects, Japanese-Brazilians (JB) and non-Japanese Brazilians (NJB). We performed a cross-sectional comparison of IgG antibody titers to CagA (CagA-Ab) and the combination of CagA-Ab with conventional surface antigen (Hp-Ab) in 80 JB and 178 NJB ncGC patients and their controls (160 JB and 178 NJB). The level of CagA-Ab titer in cancer cases was significantly higher in NJB than in JB. The strength of the association between CagA-Ab seropositivity (+) (>10 U/ml) and ncGC was almost 2-fold higher in NJB than in JB [odds ratio (OR) (95% confidence interval), 4.5 (2.6–7.8) and 2.1 (1.2–3.6), respectively]. However, in both JB and NJB, the OR was highest in CagA-Ab(+) subjects with low titer (10–29 U/ml), and decreased inversely with elevating CagA-Ab titer. In addition, the serological status of CagA-Ab(+) and Hp-Ab(-) showed a similar close association with ncGC between JB and NJB [5.4 (1.9–15.3) and 5.4 (2.0–15.0), respectively]. These results suggest that although the roles of CagA in the carcinogenic process of ncGC might be different between JB and NJB, the CagA-Ab could be a useful marker for ncGC, independently of ethnicity, particularly in high-risk individuals with the serological status of CagA-Ab(+) with low IgG titer or combined with Hp-Ab(-). (Cancer Sci 2003; 94: 64–69)
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