Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
Intervalo de ano de publicação
1.
Mol Immunol ; 90: 33-41, 2017 10.
Artigo em Inglês | MEDLINE | ID: mdl-28668455

RESUMO

Asthma is a heterogeneous disease associated with a complex basis involving environmental factors and individual variabilities. The DENN Domain Containing 1B (DENND1B) gene has an important role on T cell receptor (TCR) down-regulation on Th2 cells and studies have shown that mutations or loss of this factor can be associated with increased Th2 responses and asthma. The aim of this work is to evaluate the association of polymorphisms in the DENND1B with asthma and allergy markers phenotypes in Brazilian children. Genotyping was performed using a commercial panel from Illumina (2.5 Human Omni bead chip) in 1309 participants of SCAALA (Social Change, Asthma, Allergy in Latin American) program. Logistic regressions for asthma and atopy markers were performed using PLINK software 1.9. The analyzes were adjusted for sex, age, helminth infections and ancestry markers. The DENND1B gene was associated with different phenotypes such as severe asthma and atopic markers (specific IgE production, skin prick test and IL-13 production). Among the 166 SNPs analyzed, 72 were associated with asthma and/or allergy markers. In conclusion, polymorphisms in the DENND1B are significantly associated with development of asthma and atopy and these polymorphisms can influence DENND1B expression and consequently, asthma.


Assuntos
Asma/genética , Proteínas Adaptadoras de Sinalização de Receptores de Domínio de Morte/genética , Predisposição Genética para Doença , Fatores de Troca do Nucleotídeo Guanina/genética , Hipersensibilidade Imediata/genética , Adolescente , Asma/imunologia , Brasil , Criança , Pré-Escolar , Citocinas/biossíntese , Feminino , Estudos de Associação Genética , Humanos , Hipersensibilidade Imediata/imunologia , Imunoglobulina E/sangue , Masculino , Polimorfismo de Nucleotídeo Único/genética , Inquéritos e Questionários , Células Th2/imunologia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA