SERUM ANTIBODIES AGAINST HELICOBACTER-PYLORI PROTEINS VACA AND CAGA ARE ASSOCIATED WITH INCREASED RISK FOR GASTRIC ADENOCARCINOMA

Citation
J. Rudi et al., SERUM ANTIBODIES AGAINST HELICOBACTER-PYLORI PROTEINS VACA AND CAGA ARE ASSOCIATED WITH INCREASED RISK FOR GASTRIC ADENOCARCINOMA, Digestive diseases and sciences, 42(8), 1997, pp. 1652-1659
Citations number
50
Categorie Soggetti
Gastroenterology & Hepatology
ISSN journal
01632116
Volume
42
Issue
8
Year of publication
1997
Pages
1652 - 1659
Database
ISI
SICI code
0163-2116(1997)42:8<1652:SAAHPV>2.0.ZU;2-7
Abstract
Infection with Helicobacter pylori is associated with the development of gastric cancer. To study whether the infection with H. pylori strai ns expressing the vacuolating cytotoxin (VacA) and/or the cytotoxin-as sociated protein (CagA) is associated with an increased risk of develo ping gastric adenocarcinoma, sera of 90 patients with gastric cancer a nd 90 matched controls with cardiovascular diseases were investigated for the presence of antibodies to VacA and CagA by immunoblot. Althoug h no significant difference in the overall H. pylori seropositivity wa s found between cancer patients and controls, antibodies against VacA or CagA were significantly more frequent in cancer patients than in co ntrol subjects. Seventy-five (97.4%) of 77 H. pylori-positive patients in the cancer group, but only 60 (84.5%) of 71 H. pylori-positive con trol patients had antibodies against either VacA or CagA (chi(2) = 6.6 3; relative risk, 2.00; 95% confidence interval, 1.18-3.39; P = 0.01). The presence of antibodies against VacA or CagA alone was also associ ated with an increased cancer risk (92.2% vs 80.3%; chi(2) = 5.30; rel ative risk, 1.74; 95% confidence interval, 1.08-2.78; P = 0.021, for V acA; and 87.0% vs 74.6%; chi(2) = 4.90; relative risk, 1.61; 95% confi dence interval, 1.06-2.45; P = 0.037, for CagA). The relative risk far gastric cancer was mainly elevated in patients under 65 years, but no t in patients at or over 65 years. There is evidence that infection wi th VacA- or CagA-producing H. pylori strains increases the risk of dev eloping gastric cancer, especially in younger patients.