...
首页> 外文期刊>Comparative and functional genomics >Association of Polymorphisms in the HumanIL4andIL5Genes with Atopic Bronchial Asthma and Severity of the Disease
【24h】

Association of Polymorphisms in the HumanIL4andIL5Genes with Atopic Bronchial Asthma and Severity of the Disease

机译:HumanIL4和IL5基因多态性与特应性支气管哮喘和疾病严重程度的关系

获取原文
           

摘要

Two polymorphisms in theIL4(G/C 3′-UTR) andIL5(C-703T) genes were studied in a sample of families whose probands had atopic bronchial asthma (BA) (66 families,n = 183) and in a group of non-cognate individuals with the severe form of the disease(n = 34). The samples were collected from the Russian population in the city of Tomsk(Russia). Using the transmission/disequilibrium test (TDT), a significant associationof allele C-703IL5with BA was established (TDT = 4.923,p= 0.007 ± 0.0007). Theanalysis of 40 individuals with mild asthma and 49 patients with the severe formof the disease revealed a negative association of genotype GGIL4(OR = 0.39, 95%CI = 0.15?0.99,p= 0.035), and also a trend towards a positive association of theGCIL4genotype (OR = 2.52, 95% CI = 0.98?6.57,p= 0.052) with mild BA. Therewas a concordance of the clinical classification of BA severity with the ‘genotype’(McNemar'sχ2test with continuity correction constituted 0.03, d.f. = 1,p= 0.859).These results suggest that polymorphisms in theIL4andIL5genes contribute to thesusceptibility to atopic BA and could determine the clinical course of the disease.
机译:在先证者患有特应性支气管哮喘(BA)的家庭(66个家庭,n = 183)和一组非IL4(G / C 3'-UTR)和IL5(C-703T)基因中研究了两个多态性。 -患有严重疾病的同伴(n = 34)。样本是从俄罗斯托木斯克市的俄罗斯人口中收集的。使用传输/不平衡测试(TDT),建立了等位基因C-703IL5与BA的显着关联(TDT = 4.923,p = 0.007±0.0007)。对40例轻度哮喘患者和49例严重疾病患者的分析显示,基因型GGIL4呈负相关(OR = 0.39,95%CI = 0.15?0.99,p = 0.035),并且呈正相关的趋势。具有轻度BA的GCIL4基因型(OR = 2.52,95%CI = 0.98?6.57,p = 0.052)。 BA严重程度的临床分类与“基因型”一致(McNemar的χ2检验,经连续性校正构成0.03,df = 1,p = 0.859)。这些结果表明IL4和IL5基因的多态性有助于特应性BA的敏感性,并可以确定该疾病的临床过程。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号