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Lack of association between the CC genotype of the rs7903146 polymorphism in the TCF7L2 gene and rheumatoid arthritis.
Mota, Licia Maria Henrique da; Rabelo, Francieli de Souza; Lima, Francisco Aires Corrêa; Lima, Rodrigo Aires Corrêa; Carvalho, Jozélio Freire de; Barra, Gustavo Barcelos; Amato, Angélica Amorim.
Afiliação
  • Mota LM; Serviço de Reumatologia, Faculdade de Medicina, Universidade de Brasília, Brasília, DF, Brazil. liciamhmota@yahoo.com.br
Rev Bras Reumatol ; 52(4): 523-8, 2012 Aug.
Article em En, Pt | MEDLINE | ID: mdl-22885420
INTRODUCTION: TCF7L2 is a transcription factor involved in Wnt/beta-catenin signaling and which has a variant known to be consistently associated with type 2 diabetes risk and some studies have also indicated its association with risk of certain types of cancer. OBJECTIVE: Since this pathway may be involved in the pathophysiology of other chronic inflammatory diseases such as rheumatoid arthritis, we aimed to investigate the effect of TCF7L2 polymorphism rs7903146 on rheumatoid arthritis severity in a Brazilian population. PATIENTS AND METHODS: This polymorphism was genotyped in 208 patients with rheumatoid arthritis and in 104 healthy controls. We also analyzed the association of this polymorphism to smoking history, functional status classification and radiological indicators of disease severity. RESULTS: The distribution of CC, CT and TT genotypes of SNP rs7903146 of the TCF7L2 gene was not different between patients and controls, and no association between the genotype and indicators of disease severity or smoking history was found. When data were evaluated using the dominant model, in which carriers of the CT and TT genotypes were grouped, an increase in the T allele was observed in patients positive for rheumatoid factor and erosions, although this was not significant. The frequency of T allele was also increased in patients with functional class II compared to class I (P = 0.032). CONCLUSION: It is possible that the small number of patients included in this study may have restrained additional findings. Further studies are therefore needed to investigate the role of TCF7L2 gene variants in the risk of rheumatoid arthritis and its severity.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Polimorfismo de Nucleotídeo Único / Proteína 2 Semelhante ao Fator 7 de Transcrição / Genótipo Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En / Pt Revista: Rev Bras Reumatol Ano de publicação: 2012 Tipo de documento: Article País de afiliação: Brasil País de publicação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Polimorfismo de Nucleotídeo Único / Proteína 2 Semelhante ao Fator 7 de Transcrição / Genótipo Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En / Pt Revista: Rev Bras Reumatol Ano de publicação: 2012 Tipo de documento: Article País de afiliação: Brasil País de publicação: Brasil