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首页> 外文期刊>Molecular Genetics & Genomic Medicine >The association of nucleotide‐binding oligomerization domain 2 gene polymorphisms with the risk of asthma in the Chinese Han population
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The association of nucleotide‐binding oligomerization domain 2 gene polymorphisms with the risk of asthma in the Chinese Han population

机译:核苷酸结合寡聚化结构域2基因多态性与中国汉族人群哮喘风险的结合

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摘要

Background Genetic background is one of the important risk factors for development of asthma. The nucleotide‐binding oligomerization domain 2 ( NOD2 ) has been involved in the pathogenesis of asthma. The purpose of this study was to explore the relationship between NOD2 gene polymorphisms and asthma susceptibility in the Chinese Han population. Methods Children with asthma ( n ?=?309) and Healthy children ( n ?=?163) were recruited from Yancheng Third People's Hospital, Yancheng, China, between January 2016 and December 2017. The NOD2 gene polymorphisms were measured by the Snapshot SNP genotyping assays. Genotyping was performed for 4 tag SNPs of NOD2 . Serum IFN‐β levels were measured by ELISA. Results The serum IFN‐β levels were significantly lower in Asthmatic children than those in the controls ( p ??0.001). Low levels of IFN‐β may be related to the susceptibility to severe asthma. The rs3135499 C allele was associated with a significantly increased risk of asthma as compared with the rs3135499 A allele. Conclusion The rs3135499 polymorphism of NOD2 gene and IFN‐β may play a role in the pathogenesis of asthma.
机译:背景遗传背景是哮喘发展的重要危险因素之一。结合核苷酸结合的寡聚化结构域2(NOD2)已参与哮喘的发病机制。本研究的目的是探讨Nod2基因多态性与中国汉族人群的哮喘易感性之间的关系。方法招聘了哮喘的儿童(N?= 309)和健康的儿童(N?=?163),从2016年1月至2017年1月延城盐城市盐城市第三人民医院(N?=?163)。Nod2基因多态性由快照SNP测量基因分型测定。对NOD2的4个标签SNP进行基因分型。通过ELISA测量血清IFN-β水平。结果哮喘儿童的血清IFN-β水平明显低于对照组(p≤0.001)。低水平的IFN-β可能与对严重哮喘的敏感性有关。与vS3135499的等位基因相比,RS3135499 C等位基因与哮喘的风险显着增加。结论NOD2基因的RS3135499多态性和IFN-β可能在哮喘发病机制中发挥作用。

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