首页> 外文期刊>The journal of asthma >Association and gene-gene interactions of eight common single-nucleotide polymorphisms with pediatric asthma in middle china.
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Association and gene-gene interactions of eight common single-nucleotide polymorphisms with pediatric asthma in middle china.

机译:中国中部八种常见单核苷酸多态性与小儿哮喘的关联和基因-基因相互作用。

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BACKGROUND: Asthma is a common polygenic disease, caused by complex interactions between multiple genes and environmental factors. Study of the gene-gene interactions would contribute to a new insight into the pathogenesis and therapeutics of asthma. OBJECTIVE: To evaluate the single and combined associations of eight single-nucleotide polymorphisms loci in five candidate genes with the development of asthma in Chinese children. METHODS: We examined eight single-nucleotide polymorphisms (SNPs) in five key asthma susceptibility genes and performed single SNP association study, haplotype analysis, and gene-gene interactions analysis in 479 Chinese children, including 252 asthmatic subjects and 227 healthy controls. Genotyping was performed by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis. Haplotype analysis was detected by SHEsis software. Gene-gene interactions were tested using the multifactor dimensionality reduction (MDR) method. RESULTS: There were significant differences of interleukin (IL)-13 R130Q and IL-13 C1923T in genotype and allele frequency distributions between the asthmatic group and control group. Furthermore, the A allele of IL-13 R130Q and the T allele of IL-13 C1923T were significantly associated with increased risk of asthma (odds ratio [OR] = 1.59, 95% confidence interval [CI] 1.20-2.09, p = .0010; OR = 1.57, 95% CI 1.19-2.08, p = .0014, respectively). By haplotype analysis, the C-G and T-A haplotypes consisting of IL-13 C1923T and IL-13 R130Q and the G-A and A-A haplotypes consisting of IL-4Ralpha I75V and IL-4Ralpha Q576R were significantly associated with asthma (p < .05). Using MDR, the authors detected significant gene-gene interactions with a best six-locus model among IL-4 -C33T, IL-13 R130Q, IL-4Ralpha I75V, IL-4Ralpha Q576R, STAT6 C2892T, and CD14 -C159T on the risk of asthma (OR = 4.43, 95% CI 1.30-15.04, p < .001, by 1000-fold permutation test). CONCLUSIONS: These data suggest that genetic variants in the IL-13 gene may play an important role in the development of pediatric asthma in Middle China. In addition, the significant gene-gene interactions among IL-4 -C33T, IL-13 R130Q, IL-4Ralpha I75V, IL-4Ralpha Q576R, STAT6 C2892T, and CD14 -C159T may increase an individual's susceptibility to asthma and contribute to the pathogenesis of asthma.
机译:背景:哮喘是一种常见的多基因疾病,由多个基因和环境因素之间的复杂相互作用引起。基因与基因相互作用的研究将有助于哮喘的发病机理和治疗方法的新见解。目的:评估5个候选基因中8个单核苷酸多态性位点与哮喘患儿的单一关联和联合关联。方法:我们检查了五个关键哮喘易感基因中的八个单核苷酸多态性(SNP),并在479名中国儿童中进行了单SNP关联研究,单倍型分析和基因-基因相互作用分析,其中包括252名哮喘受试者和227名健康对照。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析进行基因分型。通过SHEsis软件检测单倍型分析。使用多维度降维(MDR)方法测试了基因与基因的相互作用。结果:哮喘组与对照组的白细胞介素(IL)-13 R130Q和IL-13 C1923T在基因型和等位基因频率分布上存在显着差异。此外,IL-13 R130Q的A等位基因和IL-13 C1923T的T等位基因与哮喘风险增加显着相关(优势比[OR] = 1.59,95%置信区间[CI] 1.20-2.09,p =)。 0010; OR = 1.57,95%CI 1.19-2.08,p = .0014)。通过单倍型分析,由IL-13 C1923T和IL-13 R130Q组成的C-G和T-A单倍型以及由IL-4Ralpha I75V和IL-4Ralpha Q576R组成的G-A和A-A单倍型与哮喘显着相关(p <.05)。使用MDR,作者检测到与最佳IL-6 -C33T,IL-13 R130Q,IL-4Ralpha I75V,IL-4Ralpha Q576R,STAT6 C2892T和CD14 -C159T六位基因模型之间显着的基因-基因相互作用。哮喘的患病率(OR = 4.43,95%CI 1.30-15.04,p <.001,经1000倍排列检验)。结论:这些数据表明IL-13基因的遗传变异可能在中国中部小儿哮喘的发展中起重要作用。此外,IL-4 -C33T,IL-13 R130Q,IL-4Ralpha I75V,IL-4Ralpha Q576R,STAT6 C2892T和CD14 -C159T之间重要的基因-基因相互作用可能会增加个体对哮喘的易感性,并助长发病机理哮喘。

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