Abstract | OBJECTIVE: METHODS: A gastric juice sample was obtained from each patient. After DNA extraction, polymerase chain reaction was used to amplify the genes urease A ( ureA), cagA, and vacA of Hp. RESULTS: A significant association was found between peptic ulcer disease and the cytotoxic genotypes, characterized by the presence of s1 and m1 alleles of vacA and by cagA. Patients with a cagA-positive genotype showed a significant increase in anti-cagA antibodies and also had significantly increased circulating levels of pepsinogen C. CONCLUSIONS: Cytotoxic Hp strains are mainly involved in determining peptic ulcer disease, but not antral gastritis. The higher levels of circulating pepsinogen C found in patients infected with cytotoxic genotypes may reflect the higher degree of inflammation sustained by these strains.
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Authors | F Navaglia, D Basso, M G Piva, L Brigato, A Stefani, N Dal Bò, F Di Mario, M Rugge, M Plebani |
Journal | The American journal of gastroenterology
(Am J Gastroenterol)
Vol. 93
Issue 2
Pg. 227-30
(Feb 1998)
ISSN: 0002-9270 [Print] United States |
PMID | 9468248
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibodies, Bacterial
- Cytotoxins
- DNA, Bacterial
- Pepsinogens
- Urease
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Antibodies, Bacterial
(analysis)
- Cytotoxins
(genetics, metabolism)
- DNA, Bacterial
(analysis)
- Duodenitis
(microbiology)
- Female
- Gastritis
(microbiology)
- Genes, Bacterial
- Genotype
- Helicobacter pylori
(genetics, immunology, metabolism)
- Humans
- Male
- Middle Aged
- Pepsinogens
(blood)
- Peptic Ulcer
(microbiology)
- Polymerase Chain Reaction
- Urease
(genetics)
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