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Analysis of filaggrin 2 gene polymorphisms in patients with atopic dermatitis,

机译:特式皮炎患者Filaggrin 2基因多态性分析,

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Background:Polymorphisms of the filaggrin 2 gene (rs 12568784 and rs 16899374) are associated with persistent atopic dermatitis in African American patients. Filaggrin 2 is a protein with a function similar to filaggrin and also encoded in the epidermal differentiation complex on chromosome 1q21.Objective:To evaluate the polymorphisms in the filaggrin 2 gene (rs 12568784 and rs 16899374) in children and adults with atopic dermatitis and to verify the association of these with the severity of the clinical picture, presence of other allergic diseases, and socio-demographic factors.Method:The study was carried out with patients and control group. Questionnaires were used to evaluate ethnicity, sex, age, family history, scoring, atopic dermatitis (SCORAD), among other parameters. Genotyping of the filaggrin 2 gene was performed by real-time polymerase chain reaction.Results:Forty-eight patients and 83 controls were evaluated. No correlation was found between the variables studied in patients with atopic dermatitis and polymorphisms, no significant difference between the prevalence of polymorphisms in the patients and in the control group p 0.05.Study limits:The exclusive use of self-reported ethnicity information and the sample size.Results:The results of this work can be an incentive for the study of the polymorphisms in atopic dermaititis, considering the characteristic of the Brazilian multi ethnic population.Conclusion:This is an unpublished work in Brazil and the first study in the world to have a control group to evaluate alterations in the gene of filaggrin 2.
机译:背景:Filaggrin 2基因的多态性(Rs 12568784和Rs 16899374)与非洲裔美国患者的持续的特应性皮炎有关。 Filaggrin 2是一种蛋白质,其具有与Filaggrin的函数,并且在染色体1Q21上的表皮分化复合物中也被编码。目的:在具有特应性皮炎的儿童和成人中,评估Fileagrin 2基因(Rs 12568784和Rs 16899374)中的多态性。通过临床图的严重程度验证这些关联,其他过敏性疾病的存在以及社会人口统计因素。方法:该研究与患者和对照组进行。问卷用于评估种族,性别,年龄,家族史,评分,特应性皮炎(Scorad)等参数。通过实时聚合酶链式反应进行Filaggrin 2基因的基因分型。结果:评估48名患者和83例对照。在特应性皮炎和多态性患者中研究的变量之间没有发现相关性,患者多态性的患病率和对照组P> 0.05的患病率没有显着差异.STUDY限制:独家使用自我报告的种族信息和样本大小。结果:考虑到巴西多族裔人口的特征,这项工作的结果可以是研究特应性DermaitIsitis的多态性。结论:这是巴西未发表的工作,并在世界上第一项研究进行对照组以评估叶片素2的基因中的改变。
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