CagA in Barrett's oesophagus in Colombia, a country with a high prevalence of gastric cancer

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Abstract

Background: In the USA, atrophic gastritis and gastric cancer are rare, whereas gastro-oesophageal reflux disease (GERD) is common. Infection with Helicobacter pylori, especially a CagA positive strain, is unusual in patients with GERD/Barrett's oesophagus in the USA. Aim: To examine the relation between Barrett's oesophagus and CagA positive H pylori in Colombia, a country with a high prevalence of CagA positive H pylori associated atrophic gastritis and gastric cancer. Methods: Helicobacter pylori and CagA status was determined among Colombian patients with long segment Barrett's oesophagus and a control group with simple H pylori gastritis. Helicobacter pylori status was determined using a triple stain and CagA status was determined by immunohistochemistry using a specific rabbit anti-CagA serum. Results: Gastric and oesophageal mucosal biopsies were obtained from 51 patients-39 men (mean age, 57.8 years; SD, 13.1) and 12 women (mean age, 51.8 years; SD, 14.4)-with documented long segment Barrett's oesophagus. The results were compared with 24 Colombian patients with H pylori gastritis without oesophageal disease. Thirty two patients with Barrett's oesophagus had active H pylori infection. CagA status was evaluated in a subset of 23 H pylori infected patients with Barrett's oesophagus, and was positive in eight of these patients compared with 19 of 24 controls (p = 0.01). Conclusions: Although most Colombian patients with Barrett's oesophagus had H pylori infection, CagA positive infections were unusual. These data illustrate how consistent corpus inflammation reduces acid secretion, which prevents Barrett's oesophagus among those with abnormal gastro-oesophageal reflux barriers.

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CITATION STYLE

APA

Kudo, M., Gutierrez, O., El-Zimaity, H. M. T., Cardona, H., Nurgalieva, Z. Z., Wu, J., & Graham, D. Y. (2005). CagA in Barrett’s oesophagus in Colombia, a country with a high prevalence of gastric cancer. Journal of Clinical Pathology, 58(3), 259–262. https://doi.org/10.1136/jcp.2004.022251

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