Association of IL1B -511C/-31T haplotype and Helicobacter pylori vacA genotypes with gastric ulcer and chronic gastritis

Background: The association between proinflammatory cytokine gene polymorphisms and gastric diseases related to Helicobacter pylori varies by population and geographic area. Our objective was to determine if the IL-1B -511 T>C and -31 C>T polymorphisms and H. pylori vacA genotypes are associat...

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Autores principales: Martínez Carrillo, Dinorah N., Garza González, Elvira, Betancourt Linares, Reyes, Mónico Manzano, Trinidad, Antúnez Rivera, Cuauhtémoc, Román Román, Adolfo, Flores Alfaro, Eugenia, Illades Aguiar, Berenice, Fernández Tilapa, Gloria
Formato: Artículo
Lenguaje:inglés
Publicado: 2010
Acceso en línea:http://eprints.uanl.mx/15079/1/738.pdf
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author Martínez Carrillo, Dinorah N.
Garza González, Elvira
Betancourt Linares, Reyes
Mónico Manzano, Trinidad
Antúnez Rivera, Cuauhtémoc
Román Román, Adolfo
Flores Alfaro, Eugenia
Illades Aguiar, Berenice
Fernández Tilapa, Gloria
author_facet Martínez Carrillo, Dinorah N.
Garza González, Elvira
Betancourt Linares, Reyes
Mónico Manzano, Trinidad
Antúnez Rivera, Cuauhtémoc
Román Román, Adolfo
Flores Alfaro, Eugenia
Illades Aguiar, Berenice
Fernández Tilapa, Gloria
author_sort Martínez Carrillo, Dinorah N.
collection Repositorio Institucional
description Background: The association between proinflammatory cytokine gene polymorphisms and gastric diseases related to Helicobacter pylori varies by population and geographic area. Our objective was to determine if the IL-1B -511 T>C and -31 C>T polymorphisms and H. pylori vacA genotypes are associated with risk of chronic gastritis and gastric ulcer in a Mexican population. Methods: We conducted endoscopic studies in 128 patients with symptoms of dyspepsia. We took two biopsies from the body, antrum, or ulcer edge from each patient, and classified our histopathological findings according to the Sydney System. H. pylori infection and vacA genotyping were accomplished via PCR from total DNA of the gastric biopsies. We confirmed the presence of anti-H. pylori serum IgG and IgM in 102 control subjects. In both case subjects and control subjects, the IL-1B -511 T>C polymorphism was genotyped by PCR-RFLPs and the IL-1B -31 C>T polymorphism was genotyped by pyrosequencing. Results: Sixty-two point seven (62.7%) of the 102 control subjects were H. pylori-seropositive. Among the case subjects, 100 were diagnosed with chronic gastritis and 28 with gastric ulcer. We found that 77% of the patients with chronic gastritis and 85.7% of the patients with gastric ulcer were H. pylori-positive. The predominant H. pylori genotype was vacA s1m1 (58.4%) and the most frequent subtype was vacA s1. The -511 TC, (rs16944 -511 T>C) genotype and the -511C allele were associated with chronic gastritis (OR = 3.1, 95% CI = 1.4-6.8 and OR = 3.0, 95% CI = 1.4-6.0, respectively). The subjects carrying -31T (rs1143627 -31 C>T) were found to be at a higher risk of having chronic gastritis (OR = 2.8, 95% CI = 1.3-5.8). The IL-1B -511C/-31T haplotype was associated with chronic gastritis (OR = 2.1, 95% CI = 1.2-3.8) but not with gastric ulcer. Conclusions: The H. pylori vacA genotypes identified herein were similar to those reported for other regions of Mexico. The vacA s1m1 genotype was not associated with gastric ulcer. In the southern Mexican population, the IL-1B -511C and -31T alleles and the -511C/-31T and -511T/-31T haplotypes are associated with increased risk of chronic gastritis and gastric ulcer.
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spelling eprints-150792020-05-25T17:55:48Z http://eprints.uanl.mx/15079/ Association of IL1B -511C/-31T haplotype and Helicobacter pylori vacA genotypes with gastric ulcer and chronic gastritis Martínez Carrillo, Dinorah N. Garza González, Elvira Betancourt Linares, Reyes Mónico Manzano, Trinidad Antúnez Rivera, Cuauhtémoc Román Román, Adolfo Flores Alfaro, Eugenia Illades Aguiar, Berenice Fernández Tilapa, Gloria Background: The association between proinflammatory cytokine gene polymorphisms and gastric diseases related to Helicobacter pylori varies by population and geographic area. Our objective was to determine if the IL-1B -511 T>C and -31 C>T polymorphisms and H. pylori vacA genotypes are associated with risk of chronic gastritis and gastric ulcer in a Mexican population. Methods: We conducted endoscopic studies in 128 patients with symptoms of dyspepsia. We took two biopsies from the body, antrum, or ulcer edge from each patient, and classified our histopathological findings according to the Sydney System. H. pylori infection and vacA genotyping were accomplished via PCR from total DNA of the gastric biopsies. We confirmed the presence of anti-H. pylori serum IgG and IgM in 102 control subjects. In both case subjects and control subjects, the IL-1B -511 T>C polymorphism was genotyped by PCR-RFLPs and the IL-1B -31 C>T polymorphism was genotyped by pyrosequencing. Results: Sixty-two point seven (62.7%) of the 102 control subjects were H. pylori-seropositive. Among the case subjects, 100 were diagnosed with chronic gastritis and 28 with gastric ulcer. We found that 77% of the patients with chronic gastritis and 85.7% of the patients with gastric ulcer were H. pylori-positive. The predominant H. pylori genotype was vacA s1m1 (58.4%) and the most frequent subtype was vacA s1. The -511 TC, (rs16944 -511 T>C) genotype and the -511C allele were associated with chronic gastritis (OR = 3.1, 95% CI = 1.4-6.8 and OR = 3.0, 95% CI = 1.4-6.0, respectively). The subjects carrying -31T (rs1143627 -31 C>T) were found to be at a higher risk of having chronic gastritis (OR = 2.8, 95% CI = 1.3-5.8). The IL-1B -511C/-31T haplotype was associated with chronic gastritis (OR = 2.1, 95% CI = 1.2-3.8) but not with gastric ulcer. Conclusions: The H. pylori vacA genotypes identified herein were similar to those reported for other regions of Mexico. The vacA s1m1 genotype was not associated with gastric ulcer. In the southern Mexican population, the IL-1B -511C and -31T alleles and the -511C/-31T and -511T/-31T haplotypes are associated with increased risk of chronic gastritis and gastric ulcer. 2010 Article PeerReviewed text en cc_by_nc_nd http://eprints.uanl.mx/15079/1/738.pdf http://eprints.uanl.mx/15079/1.haspreviewThumbnailVersion/738.pdf Martínez Carrillo, Dinorah N. y Garza González, Elvira y Betancourt Linares, Reyes y Mónico Manzano, Trinidad y Antúnez Rivera, Cuauhtémoc y Román Román, Adolfo y Flores Alfaro, Eugenia y Illades Aguiar, Berenice y Fernández Tilapa, Gloria (2010) Association of IL1B -511C/-31T haplotype and Helicobacter pylori vacA genotypes with gastric ulcer and chronic gastritis. BMC Gastroenterology, 10 (1). ISSN 1471-230X http://doi.org/10.1186/1471-230X-10-126 doi:10.1186/1471-230X-10-126
spellingShingle Martínez Carrillo, Dinorah N.
Garza González, Elvira
Betancourt Linares, Reyes
Mónico Manzano, Trinidad
Antúnez Rivera, Cuauhtémoc
Román Román, Adolfo
Flores Alfaro, Eugenia
Illades Aguiar, Berenice
Fernández Tilapa, Gloria
Association of IL1B -511C/-31T haplotype and Helicobacter pylori vacA genotypes with gastric ulcer and chronic gastritis
thumbnail https://rediab.uanl.mx/themes/sandal5/images/online.png
title Association of IL1B -511C/-31T haplotype and Helicobacter pylori vacA genotypes with gastric ulcer and chronic gastritis
title_full Association of IL1B -511C/-31T haplotype and Helicobacter pylori vacA genotypes with gastric ulcer and chronic gastritis
title_fullStr Association of IL1B -511C/-31T haplotype and Helicobacter pylori vacA genotypes with gastric ulcer and chronic gastritis
title_full_unstemmed Association of IL1B -511C/-31T haplotype and Helicobacter pylori vacA genotypes with gastric ulcer and chronic gastritis
title_short Association of IL1B -511C/-31T haplotype and Helicobacter pylori vacA genotypes with gastric ulcer and chronic gastritis
title_sort association of il1b 511c 31t haplotype and helicobacter pylori vaca genotypes with gastric ulcer and chronic gastritis
url http://eprints.uanl.mx/15079/1/738.pdf
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