The TNF-α -308 polymorphism may affect the severity of Crohn's disease

Detalhes bibliográficos
Autor(a) principal: Santana, Genoile
Data de Publicação: 2011
Outros Autores: Bendicho, Maria Teresita, Santana, Tamara Celi, Reis, Lidiane Bianca dos, Lemaire, Denise, Lyra, Andre Castro
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/19261
Resumo: OBJECTIVE: The goal of this project was to analyze the association between Crohn's disease, its clinical features, and the tumor necrosis factor alpha (TNF-α) -308 polymorphism. METHODS: This is a case-control and cross-sectional study that enrolled 91 patients with Crohn's disease and 91 controls. Patients with Crohn's disease were characterized according to the Montreal Classification, along with their clinical and surgical treatment history. Analysis of the TNF-α -308 polymorphism was performed using a commercial kit. A stratified analysis was applied using an OR (odds ratio) with a 95% confidence interval. The chi-square and Fisher's exact tests were utilized for analysis of the association between the polymorphism and the clinical features of Crohn's disease. RESULTS: The low producer predicted phenotype was present in 76.9% of Crohn's disease cases and 75.8% of controls (OR 0.94 [0.45-1.97]). The TNF2 allele and the high producer predicted phenotype were more frequent among patients with Crohn's disease penetrating behavior (p = 0.004). The TNF2 allele and the high producer predicted phenotype were also associated with a history of colectomy (p = 0.02), and the TNF2 allele was associated with small bowel resection (p = 0.03). CONCLUSIONS: The TNF-α -308 polymorphism appears to affect the severity of the disease. However, TNF-α -308 polymorphism does not appear to be important for the susceptibility in the development of Crohn's disease.
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spelling The TNF-α -308 polymorphism may affect the severity of Crohn's disease Crohn's diseaseInflammatory bowel diseaseTumor necrosis factor alphaGenetic polymorphismMixed-race OBJECTIVE: The goal of this project was to analyze the association between Crohn's disease, its clinical features, and the tumor necrosis factor alpha (TNF-α) -308 polymorphism. METHODS: This is a case-control and cross-sectional study that enrolled 91 patients with Crohn's disease and 91 controls. Patients with Crohn's disease were characterized according to the Montreal Classification, along with their clinical and surgical treatment history. Analysis of the TNF-α -308 polymorphism was performed using a commercial kit. A stratified analysis was applied using an OR (odds ratio) with a 95% confidence interval. The chi-square and Fisher's exact tests were utilized for analysis of the association between the polymorphism and the clinical features of Crohn's disease. RESULTS: The low producer predicted phenotype was present in 76.9% of Crohn's disease cases and 75.8% of controls (OR 0.94 [0.45-1.97]). The TNF2 allele and the high producer predicted phenotype were more frequent among patients with Crohn's disease penetrating behavior (p = 0.004). The TNF2 allele and the high producer predicted phenotype were also associated with a history of colectomy (p = 0.02), and the TNF2 allele was associated with small bowel resection (p = 0.03). CONCLUSIONS: The TNF-α -308 polymorphism appears to affect the severity of the disease. However, TNF-α -308 polymorphism does not appear to be important for the susceptibility in the development of Crohn's disease. Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2011-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/1926110.1590/S1807-59322011000800011Clinics; Vol. 66 No. 8 (2011); 1373-1378 Clinics; v. 66 n. 8 (2011); 1373-1378 Clinics; Vol. 66 Núm. 8 (2011); 1373-1378 1980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/19261/21324Santana, GenoileBendicho, Maria TeresitaSantana, Tamara CeliReis, Lidiane Bianca dosLemaire, DeniseLyra, Andre Castroinfo:eu-repo/semantics/openAccess2012-05-23T16:30:48Zoai:revistas.usp.br:article/19261Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2012-05-23T16:30:48Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv The TNF-α -308 polymorphism may affect the severity of Crohn's disease
title The TNF-α -308 polymorphism may affect the severity of Crohn's disease
spellingShingle The TNF-α -308 polymorphism may affect the severity of Crohn's disease
Santana, Genoile
Crohn's disease
Inflammatory bowel disease
Tumor necrosis factor alpha
Genetic polymorphism
Mixed-race
title_short The TNF-α -308 polymorphism may affect the severity of Crohn's disease
title_full The TNF-α -308 polymorphism may affect the severity of Crohn's disease
title_fullStr The TNF-α -308 polymorphism may affect the severity of Crohn's disease
title_full_unstemmed The TNF-α -308 polymorphism may affect the severity of Crohn's disease
title_sort The TNF-α -308 polymorphism may affect the severity of Crohn's disease
author Santana, Genoile
author_facet Santana, Genoile
Bendicho, Maria Teresita
Santana, Tamara Celi
Reis, Lidiane Bianca dos
Lemaire, Denise
Lyra, Andre Castro
author_role author
author2 Bendicho, Maria Teresita
Santana, Tamara Celi
Reis, Lidiane Bianca dos
Lemaire, Denise
Lyra, Andre Castro
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Santana, Genoile
Bendicho, Maria Teresita
Santana, Tamara Celi
Reis, Lidiane Bianca dos
Lemaire, Denise
Lyra, Andre Castro
dc.subject.por.fl_str_mv Crohn's disease
Inflammatory bowel disease
Tumor necrosis factor alpha
Genetic polymorphism
Mixed-race
topic Crohn's disease
Inflammatory bowel disease
Tumor necrosis factor alpha
Genetic polymorphism
Mixed-race
description OBJECTIVE: The goal of this project was to analyze the association between Crohn's disease, its clinical features, and the tumor necrosis factor alpha (TNF-α) -308 polymorphism. METHODS: This is a case-control and cross-sectional study that enrolled 91 patients with Crohn's disease and 91 controls. Patients with Crohn's disease were characterized according to the Montreal Classification, along with their clinical and surgical treatment history. Analysis of the TNF-α -308 polymorphism was performed using a commercial kit. A stratified analysis was applied using an OR (odds ratio) with a 95% confidence interval. The chi-square and Fisher's exact tests were utilized for analysis of the association between the polymorphism and the clinical features of Crohn's disease. RESULTS: The low producer predicted phenotype was present in 76.9% of Crohn's disease cases and 75.8% of controls (OR 0.94 [0.45-1.97]). The TNF2 allele and the high producer predicted phenotype were more frequent among patients with Crohn's disease penetrating behavior (p = 0.004). The TNF2 allele and the high producer predicted phenotype were also associated with a history of colectomy (p = 0.02), and the TNF2 allele was associated with small bowel resection (p = 0.03). CONCLUSIONS: The TNF-α -308 polymorphism appears to affect the severity of the disease. However, TNF-α -308 polymorphism does not appear to be important for the susceptibility in the development of Crohn's disease.
publishDate 2011
dc.date.none.fl_str_mv 2011-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/19261
10.1590/S1807-59322011000800011
url https://www.revistas.usp.br/clinics/article/view/19261
identifier_str_mv 10.1590/S1807-59322011000800011
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/19261/21324
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 66 No. 8 (2011); 1373-1378
Clinics; v. 66 n. 8 (2011); 1373-1378
Clinics; Vol. 66 Núm. 8 (2011); 1373-1378
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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