INFECTION WITH CAGA(-PYLORI STRAINS AS A POSSIBLE PREDICTOR OF RISK IN THE DEVELOPMENT OF GASTRIC ADENOCARCINOMA IN MEXICO() HELICOBACTER)

Citation
J. Torres et al., INFECTION WITH CAGA(-PYLORI STRAINS AS A POSSIBLE PREDICTOR OF RISK IN THE DEVELOPMENT OF GASTRIC ADENOCARCINOMA IN MEXICO() HELICOBACTER), International journal of cancer, 78(3), 1998, pp. 298-300
Citations number
20
Categorie Soggetti
Oncology
ISSN journal
00207136
Volume
78
Issue
3
Year of publication
1998
Pages
298 - 300
Database
ISI
SICI code
0020-7136(1998)78:3<298:IWCSAA>2.0.ZU;2-G
Abstract
Helicobacter pylori strains possessing the Cag pathogenicity island ha ve been associated with increased gastric inflammation and with duoden al ulcer. In contrast, studies on the association of cagA(+) H, pylori infections and gastric cancer have shown conflicting results. The aim of our study was to determine whether H, pylori and CagA status are a ssociated with gastric cancer in Mexico. We selected serum samples fro m 3 geographic areas with gastric cancer mortality rates per 100,000 i nhabitants of 2.5 (low risk), 4.5 (medium risk) and 6.4 thigh risk). H . pylori infection was determined by the detection of antibodies to H. pylori whole cell antigen by an enzyme-linked immunosorbent assay (EL ISA). To study the prevalence of infection with cagA(+) strains, serum IgG antibodies to CagA were determined by ELISA using a recombinant C agA antigen. Of the 2,775 individuals studied, 1,931 were H, pylori se ropositive and 1,710 had antibodies against CagA, The risk for gastric cancer in the 3 populations studied increased proportionally as infec tion with cagA+ strains increased (p < 0.001 for trend). H, pylori inf ection also showed association with gastric cancer (p < 0.05), Individ uals seropositive for CagA, but seronegative for H, pylori whole cell antigen, were more frequent in areas with higher gastric cancer rates (p < 0.01), These results support the possible role of CagA(+) status as predictor of risk for gastric adenocarcinoma in Mexico; this is in agreement with results in European and American populations, but contr ary to studies in some Asian countries. Int. J. Cancer 78:298-300, 199 8, (C) 1998 Wiley-Liss, Inc.