Genetic Susceptibility to Asthma and Genetic Interactions in the 5q31-q33 and 16p11 Regions in Sudanese Families

A. Osman, M. Amin, H. Salah, O. Abdelaziz, M. Ibrahim
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引用次数: 1

Abstract

Background: Asthma is a complex disorder with heterogeneous phenotypes attributed to the interactions of many genes and the environment. Numerous genetic studies have mapped asthma susceptibility genes to a region on chromosome 5q31-q33. This study aimed to determine the association of 10 candidate polymorphisms in IL-4, IL-5, IL-9, IL-13 and IL-4R genes in 5q31-q33 region with susceptibility to asthma in Sudanese families.Method: Fifty two multi cases families consisting of 141 known cases of asthma and 129 healthy individuals from Khartoum state were genotyped for seven SNPs on 5q31-33 region located in four candidate genes; IL4, IL5 IL13, IL9 and three SNPs in IL4Rα on chromosome 16p using multiplex PCR with Mass ARRAY system. Multiple logistic regression was used to test for association of asthma. P-value needed to achieve statistical significance taking multiple testing into account is P=0.005 (=0.05/10 (number of SNPs genotyped)). However, since SNPs within genes showed some degree of linkage disequilibrium and SNPs were selected as major SNPs for association with Asthma in other populations. Therefore, P £ 0.01 (=0.05/5 genes) can used as the P-value required to achieve correction for multiple testing.Result: Genotype and allelic frequencies of all SNPs were similar in both asthmatics and healthy subjects. Stepwise logistic regression demonstrated that SNP IL-13 rs2069743 was markedly associated with Asthma (P=0.008) and same SNP added significant main effects to IL-4 rs2070874 or IL-9 rs31563, whereas the reverse was not true, indicating that the main effect for association with asthma in this population is most strongly tagged by SNP IL-13 rs2069743.Conclusion: There is strong genetic association of SNPs in 5q31-q33 and 16p11 region and asthma.
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苏丹家族5q31-q33和16p11区域哮喘遗传易感性和遗传相互作用
背景:哮喘是一种具有异质性表型的复杂疾病,归因于许多基因和环境的相互作用。许多遗传学研究已经将哮喘易感基因定位到染色体5q31-q33上的一个区域。本研究旨在确定苏丹家族5q31-q33区域IL-4、IL-5、IL-9、IL-13和IL-4R基因10个候选多态性与哮喘易感性的关系。方法:对来自喀土穆州的52个多病例家族(141例已知哮喘病例和129例健康个体)进行4个候选基因5q31-33区7个snp的基因分型;16p染色体上IL4, IL5, IL13, IL9和IL4Rα的三个snp的多重PCR分析采用多元逻辑回归检验哮喘的相关性。考虑多重检验达到统计学显著性所需的P值为P=0.005 (=0.05/10 (snp基因分型数))。然而,由于基因内的snp表现出一定程度的连锁不平衡,因此在其他人群中,snp被选为与哮喘相关的主要snp。因此,P£0.01(=0.05/5个基因)可以作为多重检验校正所需的P值。结果:哮喘患者与健康人群snp基因型及等位基因频率相似。逐步logistic回归结果显示,SNP IL-13 rs2069743与哮喘显著相关(P=0.008),相同的SNP增加了IL-4 rs2070874或IL-9 rs31563的显著主效应,而相反则不正确,说明该人群中与哮喘相关的主效应被SNP IL-13 rs2069743标记得最强烈。结论:5q31-q33和16p11区域snp与哮喘存在较强的遗传关联。
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