Helicobacter pylori genotypes in children from a population at high gastric cancer risk:: No association with gastroduodenal histopathology

被引:14
作者
Costa Lopes, Ana Isabel
Palha, Ana
Monteiro, Lurdes
Olcastro, Monica
Pelerito, Ana
Fernandes, Afonso
机构
[1] Univ Hosp Santa Maria, Gastroenterol Unit, Dept Pediat, P-1649028 Lisbon, Portugal
[2] Univ Hosp Santa Maria, Dept Pathol, P-1649028 Lisbon, Portugal
[3] Natl Inst Hlth, INSA, Helicobacter Unit, Dept Bacteriol, Lisbon, Portugal
关键词
D O I
10.1111/j.1572-0241.2006.00732.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVES: Both bacterial and host determinants underlying differences in histopathology and clinical outcome in H. pylori pediatric infection, as compared to adults, are still poorly documented. Pediatric studies may provide important insights on H. pylori infection immunopathogenesis, particularly in high gastric cancer risk populations. The present study concerns H. pylori genotypic diversity of isolates in children from a population with high gastric cancer risk, and its association with demographic and clinical variables, including gastroduodenal endoscopic and histopathological features. METHODS: A total of 119 subjects (mean age 10.3 yr, 1.5-18.0 yr) with H. pylori infection were studied. H. pylori vacA, cagA, and iceA genotypes were determined (PCR) in antral-obtained primary cultures; histopathological evaluation was performed in corpus, antrum, and duodenum biopsy specimens. RESULTS: cagA-, vacA s2m2, and iceA2 were the most prevalent genotypes. No association was observed between H. pylori genotypes and subject demographic and clinical variables, with the exception of a significant association between vacA s2 genotype and lower corpus inflammation score (p < 0.03). CONCLUSIONS: In this pediatric cohort, H. pylori genotype profiles were distinct from those reported in adult subjects in the same area, with a lower prevalence of the putative more virulent genotypes. Moreover, they were not associated with clinical expression of gastroduodenal disease, suggesting the potential role of host and/or environmental factors for the development of clinical disease at a later age.
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页码:2113 / 2122
页数:10
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