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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/66840
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dc.contributor.authorDe Mattos, Luiz Carlos-
dc.contributor.authorCintra, Juliana Rodrigues-
dc.contributor.authorSanches, Fábio Eduardo-
dc.contributor.authorAlves Da Silva, Rta de Cássia Martins-
dc.contributor.authorRuiz, Milton Artur-
dc.contributor.authorMoreira, Haroldo Wilson-
dc.date.accessioned2014-05-27T11:20:25Z-
dc.date.accessioned2016-10-25T18:17:41Z-
dc.date.available2014-05-27T11:20:25Z-
dc.date.available2016-10-25T18:17:41Z-
dc.date.issued2002-03-01-
dc.identifierhttp://dx.doi.org/10.1590/S1516-31802002000200006-
dc.identifier.citationSao Paulo Medical Journal, v. 120, n. 2, p. 55-58, 2002.-
dc.identifier.issn1516-3180-
dc.identifier.urihttp://hdl.handle.net/11449/66840-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/66840-
dc.description.abstractCONTEXT: Epidemiological studies have demonstrated higher frequencies of the O blood group and the non-secretor phenotype of ABH antigens among patients suffering from peptic ulcers. Since Helicobacter pylori has been established as the main etiological factor in this disease, controversies about the associations of the ABO and Lewis blood group phenotypes and secretor and non-secretor phenotypes in relation to susceptibility towards infection by this bacillus have been presented. OBJECTIVE: To verify the frequencies of ABO, Lewis blood group phenotypes, secretor and non-secretor phenotypes in patients infected or uninfected by H. pylori. DESIGN: Cross-sectional study. SETTING: Outpatient clinic. PARTICIPANTS: One hundred and twenty patients with dyspeptic symptoms who underwent endoscopy. MAIN MEASUREMENTS: ABO and Lewis blood group phenotypes were determined by a standard hemagglutination test and the secretor and non-secretor phenotypes were evaluated by saliva samples using the inhibitor hemagglutination test. RESULTS: The diagnosis of infection, made via breath and urea tests and confirmed using polymerase chain reaction (PCR) in gastric biopsy fragments, showed the presence of H. pylori in 61.7% of the patients and absence in 38.3%. The differences between the frequencies of the ABO blood group phenotypes among infected (A 27.0%; B 12.2%; AB 4.0% and O 56.8%) and uninfected patients (A 58.7%; B 13.0%; AB 4.3% and O 24.0%) were significant. The Lewis blood type, secretor and non-secretor phenotypes showed homogeneous distribution between the groups of patients analyzed. CONCLUSIONS: Our results suggest that the infection of H. pylori can be related to ABO blood groups but not to the Lewis blood group nor to secretor and non-secretor phenotypes. Copyright©2002, Associação Paulista de Medicina.en
dc.format.extent55-58-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectABO-
dc.subjectBlood groups-
dc.subjectHelicobacter pylori-
dc.subjectLewis-
dc.subjectNon-secretor phenotype-
dc.subjectSecretor phenotype-
dc.subjectbacterial infection-
dc.subjectblood group ABO system-
dc.subjectblood group Lewis system-
dc.subjectcontrolled study-
dc.subjectdyspepsia-
dc.subjectendoscopy-
dc.subjecthemagglutination test-
dc.subjecthuman-
dc.subjectmajor clinical study-
dc.subjectoutpatient department-
dc.subjectphenotype-
dc.subjectpolymerase chain reaction-
dc.subjectsaliva-
dc.subjectstomach biopsy-
dc.subjecturea breath test-
dc.subjectadolescent-
dc.subjectadult-
dc.subjectaged-
dc.subjectblood-
dc.subjectcross-sectional study-
dc.subjectfemale-
dc.subjectHelicobacter infection-
dc.subjectmale-
dc.subjectmicrobiology-
dc.subjectABO Blood-Group System-
dc.subjectAdolescent-
dc.subjectAdult-
dc.subjectAged-
dc.subjectCross-Sectional Studies-
dc.subjectDyspepsia-
dc.subjectFemale-
dc.subjectHelicobacter Infections-
dc.subjectHemagglutination Tests-
dc.subjectHumans-
dc.subjectLewis Blood-Group System-
dc.subjectMale-
dc.subjectPhenotype-
dc.subjectPolymerase Chain Reaction-
dc.titleABO, Lewis, secretor and non-secretor phenotypes in patients infected or uninfected by the Helicobacter pylori bacillusen
dc.typeoutro-
dc.contributor.institutionFaculty of Medicine of São José do Rio Preto-
dc.contributor.institutionHemocenter of São José do Rio Preto-
dc.contributor.institutionFUNFARME-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionFaculdade de Medicina de São José do Rio Preto (FAMERP)-
dc.description.affiliationDepartment of Molecular Biology Faculty of Medicine of São José do Rio Preto, S. José do Rio Preto, SP-
dc.description.affiliationDepartment of Molecular Biology Faculty of Medicine of São José do Rio Preto-
dc.description.affiliationMolecular Immunogenetic Laboratory Hemocenter of São José do Rio Preto, São José do Rio Preto-
dc.description.affiliationDepartment of Internal Medicine Faculty of Medicine of São José do Rio Preto-
dc.description.affiliationGastroenterology Laboratory Hospital of Base FUNFARME, São José do Rio Preto-
dc.description.affiliationBone Marrow Transplant Unit Hospital of Base FUNFARME, São José do Rio Preto-
dc.description.affiliationDepartment of Clinical Analyses Faculty of Pharmaceutical Sciences São Paulo State University, São Paulo-
dc.description.affiliationDepartamento de Biologia Molecular Faculdade de Medicina de São José do Rio Preto, Avenida Brigadeiro Faria Lima, 5416, S. J. do R. Preto/SP - CEP 15090-000-
dc.description.affiliationUnespDepartment of Clinical Analyses Faculty of Pharmaceutical Sciences São Paulo State University, São Paulo-
dc.identifier.doi10.1590/S1516-31802002000200006-
dc.identifier.scieloS1516-31802002000200006-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-0037034506.pdf-
dc.relation.ispartofSão Paulo Medical Journal-
dc.identifier.scopus2-s2.0-0037034506-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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