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vacA genotypes in oral cavity and Helicobacter pylori seropositivityamong adults without dyspepsia
Román-Román, Adolfo; Fernández-Tilapa, Gloria; Martínez-Carrillo, Dinorah-Nashely; Axinecuilteco-Hilera, Jazmín; Giono-Cerezo, Silvia; Illades-Aguiar, Berenice.
Afiliação
  • Román-Román, Adolfo; Universidad Autónoma de Guerrero. Unidad Académica de Ciencias Químico Biológicas. Laboratorio de Investigación Clínica. Guerrero. México
  • Fernández-Tilapa, Gloria; Universidad Autónoma de Guerrero. Unidad Académica de Ciencias Químico Biológicas. Laboratorio de Investigación Clínica. Guerrero. México
  • Martínez-Carrillo, Dinorah-Nashely; Universidad Autónoma de Guerrero. Unidad Académica de Ciencias Químico Biológicas. Laboratorio de Investigación Clínica. Guerrero. México
  • Axinecuilteco-Hilera, Jazmín; Universidad Autónoma de Guerrero. Unidad Académica de Ciencias Químico Biológicas. Master’s student in Biomedical Sciences. Guerrero. México
  • Giono-Cerezo, Silvia; Instituto Politécnico Nacional. Escuela Nacional de Ciencias Biológicas. Departamento de Microbiología. s. c. México
  • Illades-Aguiar, Berenice; Universidad Autónoma de Guerrero. Unidad Académica de Ciencias Químico Biológicas. Laboratorio de Biomedicina Molecular. Guerrero. México
Med. oral patol. oral cir. bucal (Internet) ; 16(2): 175-180, mar. 2011. tab
Article em En | IBECS | ID: ibc-92981
Biblioteca responsável: ES1.1
Localização: BNCS
RESUMEN
Objective: The aims of this research were to determine the prevalence of Helicobacter pylori and its vacA genotypesin oral cavity in persons without dyspepsia and to establish the association between the presence of H. pylori in oralcavity and oral hygiene. The seroprevalence of anti-H. pylori antibodies and its associated factors were analyzed too.Study design: For the study, 200 adults without dyspepsia symptoms were selected. Dental plaque and salivasamples from each subject were obtained. H. pylori detection in oral samples was carried out by polymerase chainreaction (PCR) and for vacA genotyping a semi-nested and nested PCR was used. The enzyme-linked immunosorbentassay (ELISA) was used to detect anti-H. pylori IgG and IgM. The data were analyzed with Chi squareand Fisher exact test and the statistical significance was set to 0.05.Results: Of 200 subjects tested, 124 (62%) were seropositive. H. pylori was detected in the oral cavity of 34subjects (17%) and vacA allelotypes were typified in 12 of those samples. The s1 allele was detected in 8 (66.7%)samples and in one of them m1 and m2 alleles were found. In four subjects vacA m1 subtypes were found and intwo of those both m1 and m2 alleles were detected. The prevalence of H. pylori in oral cavity was higher (l8.5%)among seropositive subjects compared with seronegative persons. No association was found between the presenceof H. pylori and oral hygiene habits.Conclusions: The presence of H. pylori in oral cavity is more frequent in seropositive subjects without dyspepsiasymptoms and could represent the source of gastric infection and bacterial transmission. The data suggest thatmore than one H. pylori strain may exist in the mouth of asymptomatic persons (AU)
Assuntos
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Base de dados: IBECS Assunto principal: Infecções por Helicobacter / Placa Dentária / Genótipo Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2011 Tipo de documento: Article
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Base de dados: IBECS Assunto principal: Infecções por Helicobacter / Placa Dentária / Genótipo Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2011 Tipo de documento: Article