Despite the fact that the association of Helicobacter pylori with an increa
sed risk of gastric cancer is well documented, the exact mechanisms of this
association have not been elucidated. Our aim was to shed some light on th
ese mechanisms by studying the relationship of H. pylori CagA status to gas
tric cell proliferation and apoptosis, since both play an important role in
gastrointestinal epithelial cell turnover and carcinogenesis. We studied f
ifty patients [32 men, 18 women, median age 39.5 years (range 18-67)], refe
rred for upper gastrointestinal endoscopy, from whom antral biopsies were t
aken. On biopsy specimens gastritis was estimated by scoring the severity o
f inflammatory infiltrate, and the presence of atrophy and intestinal metap
lasia were also noted. The gastric cell proliferation index (PI) was estima
ted by AgNOR staining, the epithelial apoptotic index (AI) was measured by
special staining for apoptosis, and CagA status was determined serologicall
y by immunoblotting the sera of patients against H, pylori antigens. Thirty
-eight (76%) of the 50 patients were H; pylori (positive) and 12 (24%) H. p
ylori (negative). Among the 38 H. pylori(+) patients, 28 (73.6%) were CagA(
+) and 10 (24.6%) CagA(-). In the H. pylori CagA(+) and CagA(-) groups, the
PI values [median (ranges)] were 5 (4-7) and 3.7 (3.5-5.5), respectively (
P < 0.05). In addition the difference in PI between the H. pylori CagA(+) a
nd H. pylori(-) groups was highly significant (P < 0.001). Concerning apopt
osis, in the H. pylori CagA(+) and CagA(-) groups, the values for AI were 1
(1-30) and 5.5 (1-35), respectively (P < 0.05). In addition, the differenc
e in AI between the H. pylori CagA(-) and H. pylori(-) groups, was signific
ant (P < 0.05). We conclude that H. pylori CagA(+) strains induce increased
gastric cell proliferation, which is not accompanied by a parallel increas
e in apoptosis. This might explain the increased risk for gastric carcinoma
that is associated with infection by H. pylori CagA(+) strains.