Relationship between Helicobacter pylori iceA, cagA, and vacA status and clinical outcome: Studies in four different countries
- Authors
- Yamaoka, Y; Kodama, Y; Gutierrez, O; Kim, JG; Kashima, K; Graham, DY
- Issue Date
- Jul-1999
- Publisher
- AMER SOC MICROBIOLOGY
- Keywords
- H. pylori; clinical outcome
- Citation
- JOURNAL OF CLINICAL MICROBIOLOGY, v.37, no.7, pp 2274 - 2279
- Pages
- 6
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF CLINICAL MICROBIOLOGY
- Volume
- 37
- Number
- 7
- Start Page
- 2274
- End Page
- 2279
- URI
- https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/37757
- DOI
- 10.1128/JCM.37.7.2274-2279.1999
- ISSN
- 0095-1137
1098-660X
- Abstract
- There is continuing interest in identifying Helicobacter pylori virulence factors that might predict the risk for symptomatic clinical outcomes. It has been proposed that iceA and cagA genes are such markers and can identify patients with peptic ulcers. We compared H. pylori isolates from four countries, looking at the cagA and vacA. genotypes, iceA alleles, and presentation of the infection. We used PCR to examine iceA, vacA, and cagA status of 424 H. pylori isolates obtained from patients with different clinical presentations (peptic ulcer, gastric cancer, and atrophic gastritis), The H, pylori isolates examined included 107 strains from Bogota, Colombia, 70 from Houston, Tex,, 135 from Seoul, Korea, and 112 from Kyoto, Japan. The predominant genotype differed among countries: the cagA-positive iceA1 vacA slc-ml genotype was predominant in Japan and Korea, the cagA-positive iceA2 vacA s1b-m1 genotype nas predominant in the United States, and the cagA-positive iceA2, vacA sla-ml genotype was predominant in Colombia, There was no association between the iceA, vacA, or cagA status and clinical outcome in patients in the countries studied. iceA status shows considerable geographic differences, and neither iceA nor combinations of iceA, vacA, and cagA were helpful in predicting the clinical presentation of an H. pylori infection.
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Collections - 2. Clinical Science > Department of Internal Medicine > 1. Journal Articles
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