Literature DB >> 10799946

Clinical relevance of Helicobacter pylori CagA-positive strains: gastroduodenal peptic lesions marker.

J M Martín Guerrero1, P Hergueta Delgado, J Esteban Carretero, R Romero Castro, F J Pellicer Bautista, J M Herrerías Gutiérrez.   

Abstract

OBJECTIVES: peptic ulcer is characterized by its recurrent nature, which necessitates maintenance treatment in most patients. But this natural history can be changed in patients with peptic ulcer associated to Helicobacter pylori, as shown by the low rates of recurrence and decreased hemorrhagic recidivism associated with this infection. Whether CagA or VacA strains are associated with a greater risk of peptic ulcer is controversial. This study was designed to examine endoscopic findings and their relation with H. pylori phenotype (CagA or VacA).
METHODS: 106 selected dyspeptic patients underwent upper gastrointestinal tract endoscopic examination between September 1996 and May 1997 [69 with H. pylori (Hp) and 37 without this infection]. Endoscopic findings were classified as gastric ulcer (GU), duodenal ulcer (DU), gastric erosions (GE), duodenitis (Du), chronic gastritis (CG) and normal mucosa (NM). Hp phenotype was analyzed with a western blot test.
RESULTS: 75% of H. pylori strains were CagA-positive and 54.2% were VacA-positive. 82.4% of the cases of DU were associated with a CagA+ phenotype, but the association was not statistically significant. Otherwise 100% of gastric ulcers were associated with CagA+ strains (p < 0.005). VacA phenotype was not associated with any particular endoscopic finding. Peptic ulcer (DU or GU) was also associated with the CagA+ phenotype (p < 0.05).
CONCLUSIONS: the CagA+ H. pylori phenotype seems to be a peptic lesion marker, but was more frequently related with GU than with DU in our sample of Spanish patients.

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Year:  2000        PMID: 10799946

Source DB:  PubMed          Journal:  Rev Esp Enferm Dig        ISSN: 1130-0108            Impact factor:   2.086


  3 in total

1.  Association of CagA and VacA presence with ulcer and non-ulcer dyspepsia in a Turkish population.

Authors:  Kantarceken Bulent; Aladag Murat; Atik Esin; Koksal Fatih; Harputluoglu MMMurat; Harputluoglu Hakan; Karincaoglu Melih; Ates Mehmet; Yildirim Bulent; Hilmioglu Fatih
Journal:  World J Gastroenterol       Date:  2003-07       Impact factor: 5.742

2.  Comparison of cytotoxin genotypes of Helicobacter pylori in stomach and saliva.

Authors:  Jie Wang; David S Chi; John J Laffan; Chuanfu Li; Donald A Ferguson; Peter Litchfield; Eapen Thomas
Journal:  Dig Dis Sci       Date:  2002-08       Impact factor: 3.199

3.  Helicobacter pylori with stronger intensity of CagA phosphorylation lead to an increased risk of gastric intestinal metaplasia and cancer.

Authors:  Chiao-Hsiung Chuang; Hsiao-Bai Yang; Shew-Meei Sheu; Kuei-Hsiang Hung; Jiunn-Jong Wu; Hsiu-Chi Cheng; Wei-Lun Chang; Bor-Shyang Sheu
Journal:  BMC Microbiol       Date:  2011-05-27       Impact factor: 3.605

  3 in total

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