There are gene polymorphisms which influence the production quantity of some cytokines. It has also been reported that certain cytokines participate in the onset of gastric cancer. It is reported that interleukin-1 beta (IL-1b) gene polymorphisms and interleukin-1 receptor antagonist (IL-1RN) gene polymorphisms are particularly associated with increased risk of gastric cancer. Furthermore, polymorphisms in the gene for cytochrome P-450 (
CYP2C19), which is a representative drug-metabolizing hepatic enzyme, are known to influence pharmacokinetics and pharmacodynamics. It is reported that
CYP2C19 participates in the onset of cancer in the esophagus, lung and liver. However, there are few reports that
CYP2C19 participates in the onset of gastric cancer. At present, persons which test positive with the serum pepsinogen (PG) method (cutoff value: lower than PG I 70ng/ml and lower than PG I/II rate 3.0) are considered to belong to the high-risk group for gastric cancer. In the current study, we examined
IL-1B and
CYP2C19 polymorphisms using multivariate analysis in order to better select high-risk cases during gastric cancer examination. We screened 228 subjects for gastric cancer [male ratio: 0.84; mean age: 45.8 +/- 0.6 years]. The serum anti-
H. pylori IgG antibody level and the presence of the
IL-1B-511 polymorphism were factors which clearly differed between the low-risk group and the high-risk group, not the serum anti-
H. pylori IgG antibody level or the presence of the
CYP2C19 polymorphism. In the multivariate analysis of these factors, the odds ratio of the serum anti-
H. pylori IgG antibody was 70.9, and that of the
IL-1B-511 polymorphism was 2.50 (i.e., the ratio between the C/C genotype and the C/T or T/T genotype). Based on our findings described above, we were able to predict cases of atrophic gastritis, which tended to develop further due to the infection by
H. pylori, based on the presence of the
IL-1B-511 polymorphism as easily as with the PG method. Thus, the use of the
IL-1B-511 polymorphism together with the PG method will enable us to more accurately select high-risk cases of gastric cancer. However, we believe that further study of this combined
IL-1B and
CYP2C19 polymorphism examination method is necessary.
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