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DENND1B基因多态性与巴西儿童的哮喘和特应性表型相关。

Polymorphisms in DENND1B gene are associated with asthma and atopy phenotypes in Brazilian children.

作者信息

Fiuza Bianca S D, Silva Milca de J, Alcântara-Neves Neuza M, Barreto Maurício L, Costa Ryan Dos S, Figueiredo Camila A

机构信息

Departamento de Biorregulação, Laboratório de Imunofarmacologia e Biologia Molecular, Universidade Federal da Bahia (ICS), Bahia, Brazil.

Fundação Oswaldo Cruz, Salvador, Bahia, Brazil.

出版信息

Mol Immunol. 2017 Oct;90:33-41. doi: 10.1016/j.molimm.2017.06.030. Epub 2017 Jun 29.

Abstract

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.

摘要

哮喘是一种异质性疾病,其发病基础复杂,涉及环境因素和个体差异。含DENN结构域蛋白1B(DENND1B)基因在Th2细胞的T细胞受体(TCR)下调中起重要作用,研究表明该因子的突变或缺失可能与Th2反应增强及哮喘有关。本研究旨在评估巴西儿童中DENND1B基因多态性与哮喘及过敏标志物表型之间的关联。采用Illumina公司的商业芯片(2.5人类全基因组珠芯片)对1309名参与SCAALA(拉丁美洲社会变革、哮喘、过敏)项目的受试者进行基因分型。使用PLINK软件1.9对哮喘和特应性标志物进行逻辑回归分析。分析针对性别、年龄、蠕虫感染和祖先标志物进行了校正。DENND1B基因与不同表型相关,如重度哮喘和特应性标志物(特异性IgE产生、皮肤点刺试验和IL-13产生)。在分析的166个单核苷酸多态性(SNP)中,72个与哮喘和/或过敏标志物相关。总之,DENND1B基因多态性与哮喘和特应性的发生显著相关,这些多态性可影响DENND1B的表达,进而影响哮喘。

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