The importance of vacA, cagA, and iceA genotypes of Helicobacter pylori infection in peptic ulcer disease and gastroesophageal reflux disease

被引:0
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作者
Arents, NLA
van Zwet, AA
Thijs, JC
Kooistra-Smid, AMD
van Slochteren, KR
Degener, JE
Kleibeuker, JH
van Doorn, LJ
机构
[1] Bethesda Hosp, Dept Gastroenterol, NL-7909 AA Hoogovens, Netherlands
[2] Reg Publ Hlth Lab, Groningen, Netherlands
[3] Univ Groningen Hosp, Dept Med Microbiol, Groningen, Netherlands
[4] Univ Groningen Hosp, Dept Gastroenterol, Groningen, Netherlands
[5] Delft Diagnost Lab, Delft, Netherlands
来源
AMERICAN JOURNAL OF GASTROENTEROLOGY | 2001年 / 96卷 / 09期
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中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVE: To study the relationship between the presence of H. pylori virulence factors and clinical outcome in H. pylori infected patients. METHODS: DNA was isolated from an antral biopsy sample and vacA, cagA, and iceA genotype were determined by PCR and a reverse hybridization technique in 183 patients with culture-proven H. pylori infection: 51 with peptic ulcer disease (PUD), 62 with gastroesophageal. reflux disease (GERD), and 70 with a normal endoscopy (gastritis only; GO). RESULTS: Forty-four samples (24%) showed more than one allelic variant in the vacA s- or m-region and/or both iceA1 and iceA2 genotypes, indicating multiple strain infection. These were excluded from statistical analysis. vacA sl and cagA were significantly more common in PUD than in GERD and GO. Logistic regression analysis showed that GERD patients were more often infected with strains lacking both ca-A and iceA than GO patients (OR = 0.36; CI = 0.15-0.89). Trend analysis showed that GERD patients were most often infected with less virulent strains (p < 0.002). CONCLUSION: Multiple strain infection is common. H. pylori strains possessing the vacA sl genotype and/or cagA are associated with PUD. GERD patients, infected with H. pylori, mostly carry less virulent strains possessing neither ca-A nor iceA1. Our findings support the hypothesis that virulent strains protect against the development of GERD. (Am J Gastroenterol 2001;96:2603-2608. (C) 2001 by Am. Coll. of Gastroenterology).
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页码:2603 / 2608
页数:6
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