Literature DB >> 19702906

Distribution of Helicobacter pylori cagA, cagE, oipA and vacA in different major ethnic groups in Tehran, Iran.

Hossein Dabiri1, Parviz Maleknejad, Yoshio Yamaoka, Mohammad M Feizabadi, Fereshteh Jafari, Maryam Rezadehbashi, Farrokh A Nakhjavani, Akbar Mirsalehian, Mohammad R Zali.   

Abstract

BACKGROUND AND AIM: There are geographical variations in Helicobacter pylori virulence genes; cagA, cagE, vacA and oipA. The present study compared the distribution of these genotypes in major ethnic groups residing in Tehran, Iran and their association with clinical outcomes.
METHODS: A total of 124 H. pylori-positive patients living in Tehran were enrolled in this study. The ethnic distribution was 74 Persians, 33 Turks and 17 other ethnics including Kurds, Lurs, Afghanis and Arabs. The presence of the cagA, cagE and oipA genes and vacA alleles (signal [s] and middle [m] region) were determined by polymerase chain reaction (PCR) from H. pylori DNA.
RESULTS: The cagA-positive status was predominant in all three ethnic groups (e.g. 65% in Persians and 73% in Turks). In contrast, the cagE-positive status was less than half in Persians (47%) and Turks (30%), whereas it was 77% in other ethnicities (P = 0.008). The predominant vacA genotypes were s1 and m1 in all three ethnic groups (e.g. 68% in Persians and 70% in Turks were s1). There was no significant association between cagA and cagE status or vacA genotypes and clinical outcomes. The oipA-positive strains were more common in non-ulcer dyspepsia (NUD) (63%) than in peptic ulcer patients (15%) (P = 0.001) in Persians, but the association was not observed in other ethnic groups.
CONCLUSION: There are some differences in the H. pylori genotypes among the ethnic groups in Iran. However, none of these markers seemed to be clinically helpful in predicting the clinical presentation of a H. pylori infection in Iran.

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Year:  2009        PMID: 19702906      PMCID: PMC3128249          DOI: 10.1111/j.1440-1746.2009.05876.x

Source DB:  PubMed          Journal:  J Gastroenterol Hepatol        ISSN: 0815-9319            Impact factor:   4.029


  48 in total

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Authors:  B C Wong; Y Yin; D E Berg; H H Xia; J Z Zhang; W H Wang; W M Wong; X R Huang; V S Tang; S K Lam
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2.  The Helicobacter pylori vacA s1, m1 genotype and cagA is associated with gastric carcinoma in Germany.

Authors:  S Miehlke; C Kirsch; K Agha-Amiri; T Günther; N Lehn; P Malfertheiner; M Stolte; G Ehninger; E Bayerdörffer
Journal:  Int J Cancer       Date:  2000-08-01       Impact factor: 7.396

3.  A M(r) 34,000 proinflammatory outer membrane protein (oipA) of Helicobacter pylori.

Authors:  Y Yamaoka; D H Kwon; D Y Graham
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-20       Impact factor: 11.205

4.  Polymorphisms of Helicobacter pylori HP0638 reflect geographic origin and correlate with cagA status.

Authors:  T Ando; R M Peek; D Pride; S M Levine; T Takata; Y-C Lee; K Kusugami; A van der Ende; E J Kuipers; J G Kusters; M J Blaser
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5.  Importance of Helicobacter pylori oipA in clinical presentation, gastric inflammation, and mucosal interleukin 8 production.

Authors:  Yoshio Yamaoka; Shogo Kikuchi; Hala M T el-Zimaity; Oscar Gutierrez; Michael S Osato; David Y Graham
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Authors:  M Mohammadi; A Oghalaie; N Mohajerani; S Massarrat; M Nasiri; M Bennedsen; H Colding; L P Andersen
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7.  Analysis of the vacA, cagA, cagE, iceA, and babA2 genes in Helicobacter pylori from sixty-one pediatric patients from the Midwestern United States.

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Journal:  J Clin Microbiol       Date:  2003-08       Impact factor: 5.948

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  28 in total

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2.  Clinical relevance of cagL gene and virulence genotypes with disease outcomes in a Helicobacter pylori infected population from Iran.

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Authors:  Mohammad Rostami Nejad; Kamran Rostami; Yoshio Yamaoka; Reza Mashayekhi; Mahsa Molaei; Hossein Dabiri; David Al Dulaimi; Dariush Mirsattari; Homayoun Zojaji; Mohsen Norouzinia; Mohammad Reza Zali
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5.  Analysis of Helicobacter pylori genotypes in Afghani and Iranian isolates.

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8.  Reciprocal impact of host factors and Helicobacter pylori genotypes on gastric diseases.

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9.  Low Rate of babA2 Genotype among Iranian Helicobacter pylori Clinical Isolates.

Authors:  Maryam Sohrabi; Reza Khashei; Mahvash Alizadeh; Mohammad-Kazem Hosseini Asl; Mohammad-Ali Nejati; Mahintaj Dara; Abdollah Bazargani
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10.  Analysis of clinical isolates of Helicobacter pylori in Pakistan reveals high degrees of pathogenicity and high frequencies of antibiotic resistance.

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Journal:  Helicobacter       Date:  2014-05-14       Impact factor: 5.753

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