论文部分内容阅读
Objective: There are two genotypes of the vacA intermediate region, i1 and i2; however, the association between the genotypes and gastroduodenal disease remains to be elucidated. The aim of this article was to investigate the interaction between the genotypes and H. pylori-associated diseases such as chronic gastritis, peptic ulcer disease(PUD) and gastric cancer. Methods: The meta-analysis was performed in Review Manager 4.2.2. Results: Eleven(ten articles and one abstract) met the inclusion criteria and were included. The i1 genotype increased the risk of PUD(OR = 1.70, 95% CI: 1.24–2.33, P < 0.001) and gastric cancer(OR = 3.90, 95% CI: 2.64–5.78, P < 0.001). Sub-analysis showed that the i1 genotype was significantly associated with gastric ulcers(OR = 2.59, 95% CI: 1.05–6.35, P = 0.040), but not with duodenal ulcers(OR = 1.04, 95% CI: 0.61–1.76, P = 0.90). In addition, the association between the i1 genotype and PUD and GC existed in studies not only from Europe but also Asia, except for the association between the i1 genotype and PUD in Asian population. Conclusion: The vacA i1 genotype is associated with an increased risk of the development of peptic ulcer disease(mainly gastric ulcer) and gastric cancer. In geographical distribution, the association between the i1 genotype and PUD and GC existed in studies not only from Europe but also Asia, except for the association between the i1 genotype and PUD in Asian population.
Objective: There are two genotypes of the vacA intermediate region, i1 and i2; however, the association between the genotypes and gastroduodenal disease remains to be elucidated. The aim of this article was to investigate the interaction between the genotypes and H. pylori-associated Methods: The meta-analysis was performed in Review Manager 4.2.2. Results: Eleven (ten articles and one abstract) met the inclusion criteria and were included. The Sub genotype increased the risk of PUD (OR = 1.70, 95% CI: 1.24-2.33, P <0.001) and gastric cancer (OR = 3.90, 95% CI: 2.64-5.78, P <0.001) the i1 genotype was significantly associated with gastric ulcers (OR = 2.59, 95% CI: 1.05-6.35, P = 0.040), but not with duodenal ulcers (OR = 1.04, 95% CI: 0.61-1.76, P = 0.90). In addition, the association between the i1 genotype and PUD and GC existed in studies not only from Europe but also Asi a, except for the association between the i1 genotype and PUD in Asian population. Conclusion: The vacA i1 genotype is associated with an increased risk of the development of peptic ulcer disease (mainly gastric ulcer) and gastric cancer. between the i1 genotype and PUD and GC existed in studies not only from Europe but also Asia, except for the association between the i1 genotype and PUD in Asian population.