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首页> 外文期刊>Human Immunology: Official Journal of the American Society for Histocompatibility and Immunogenetics >Tumor necrosis factor-alpha is a common genetic risk factor for asthma, juvenile rheumatoid arthritis, and systemic lupus erythematosus in a Mexican pediatric population.
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Tumor necrosis factor-alpha is a common genetic risk factor for asthma, juvenile rheumatoid arthritis, and systemic lupus erythematosus in a Mexican pediatric population.

机译:肿瘤坏死因子-α是患有哮喘,青少年类风湿性关节炎和墨西哥儿科人群的全身性红斑狼疮的常见遗传危险因素。

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摘要

There is a great deal of evidence that points to the association of the tumor necrosis factor-alpha (TNF-alpha) gene as a common genetic factor in the pathogenesis of diseases that are caused by inflammatory and/or autoimmune etiologies. Two single nucleotide polymorphisms (SNPs) identified in the TNF-alpha promoter region have been associated with disease susceptibility and severity. We investigated whether -308G/A and -238G/A TNF-alpha polymorphisms were associated with asthma, systemic lupus erythematosus (SLE), and juvenile rheumatoid arthritis (JRA) in a pediatric Mexican population. In a case-control study of 725 patients (asthma: 226, JRA: 171, and SLE: 328) and 400 control subjects, the participants were analyzed using the allelic discrimination technique. The genotype distribution of both TNF-alpha polymorphisms was in Hardy-Weinberg equilibrium in each group. However, there were significant differences in the allele frequency of TNF-alpha-308A between the patients and the healthy controls. This allele was detected in 2.9% of the controls, 6.0% of asthmatic and JRA patients (p = 0.002 and p = 0.0086), and 6.7% of SLE patients (p = 0.00049); statistical significance was maintained after ancestry stratification (asthma: p = 0.0143, JRA: p = 0.0083, and SLE: p = 0.0026). Stratification by gender showed that the risk for the -308A allele in asthma and JRA was greater in females (OR = 4.16, p = 0.0008 and OR = 4.4, p = 0.0002, respectively). The TNF-alpha -238A allele showed an association only with JRA in males (OR = 2.89, p = 0.004). These results support the concept that the TNF-alpha gene is a genetic risk factor for asthma, SLE, and JRA in the pediatric Mexican population.
机译:存在大量证据表明肿瘤坏死因子-α(TNF-α)基因作为炎症和/或自身免疫病因引起的疾病发病机制中的常见遗传因素。在TNF-α启动子区中鉴定的两个单一核苷酸多态性(SNP)与疾病易感性和严重程度有关。我们研究了-308g / a和-238g / a TNF-α多态性是否与哮喘,全身狼疮红斑(SLE)和小儿墨西哥人群中的青少年类风湿性关节炎(JRA)相关。在725名患者的病例对照研究(哮喘:226,JRA:171和SLE:328)和400个对照受试者,使用等位基因辨别技术分析参与者。 TNF-α多态性的基因型分布在每组的Hardy-Weinberg平衡中。然而,患者与健康对照之间的TNF-alpha-308a等等位基因频率存在显着差异。该等位基因检测到2.9%的对照,6.0%的哮喘和JRA患者(P = 0.002和P = 0.0086),6.7%的SLE患者(P = 0.00049);血统分层后保持统计学意义(哮喘:P = 0.0143,JRA:P = 0.0083,SLE:P = 0.0026)。性别分层显示,哮喘和JRA的-308a等位基因的风险在女性中更大(或= 4.16,p = 0.0008和或= 4.4,p = 0.0002)。 TNF-α-238a等位基因仅与男性JRA(或= 2.89,P = 0.004)显示联想。这些结果支持TNF-α基因是哮喘,SLE和JRA在儿科墨西哥人群中的遗传危险因素的概念。

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