Korean J Med.  2005 Sep;69(3):264-273.

Relationship between duodenal ulcers and cagA, vacA, and iceA genotypes of Helicobacter pylori

Affiliations
  • 1Division of Gastroenterology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea. jhkm@amc.seoul.kr
  • 2Research Institute for Gastrointestinal Diseases, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.

Abstract

BACKGROUND: The aims of this study were to evaluate whether genotypes of Helicobacter pylori are different between the gastric antrum and duodenal bulb in order to assess the roles of duodenal H. pylori strains in development of duodenal ulcer.
METHODS
Forty-eight H. pylori infected patients (duodenal ulcer 28, chronic gastritis 20) were included for the study. Biopsy specimens were taken separately from the antrum and duodenal bulb for the histologic examination and H. pylori culture. cagA, vacA, and iceA genotypes of H. pylori were examined by polymerase chain reaction and H. pylori DNA subtypes by random amplified polymorphic DNA (RAPD) fingerprinting.
RESULTS
H. pylori genotypes were not significantly different between antrum and duodenal bulb of the duodenal ulcer and chronic gastritis. RAPD fingerprinting showed different H. pylori strains between the gastric antrum and duodenal bulb in 2 patients with duodenal ulcer. Most prevalent genotype was cagA+ vacA s1/m1 iceA1 in duodenal ulcer (15/16).
CONCLUSION
The host factor or other genotypes may play the major roles in duodenal ulcerogenesis compared with H. pylori genotype itself.

Keyword

Helicobacter pylori; Duodenal ulcer; Chronic gastritis; Genotypes

MeSH Terms

Biopsy
Dermatoglyphics
DNA
Duodenal Ulcer*
Gastritis
Genotype*
Helicobacter pylori*
Helicobacter*
Humans
Polymerase Chain Reaction
Pyloric Antrum
Ulcer
DNA
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