首页> 外国专利> RAB1A GENE POLYMORPHISMS IN AERD AND BIOMARKER AND KIT FOR DIAGNOSISING AND DISTINGUSHING AERD INCLUDING RAB1A GENE

RAB1A GENE POLYMORPHISMS IN AERD AND BIOMARKER AND KIT FOR DIAGNOSISING AND DISTINGUSHING AERD INCLUDING RAB1A GENE

机译:用于诊断和区分包括RAB1A基因在内的Aerd,生物标志物和试剂盒中的RAB1A基因多态性

摘要

The present invention relates to a marker composition including RAB1A genes for aspirin-exacerbated respiratory diseases (AERD) and a diagnostic kit thereof. More specifically, the AERD diagnosis marker includes the single nucleotide polymorphisms (SNPs) of the RAB1A genes used as a marker for revealing the progression of AERD. The present invention investigates the relationship between the single nucleotide polymorphisms of the RAB1A genes and the AERD. In a logistic regression analysis, the minor allele frequency of +41170 CGon at intron 5 is confirmed to be significantly lower in the AERD group (n = 261) than in the ATA group (n = 1016). In a linear regression analysis, a strong relationship between the +41170 CG and the FEV1 decrease in the aspirin resistance is confirmed to exist (P= 0.01). The RAB1A genes can be crucial to the improvement of the asthmatic patient. The genetic polymorphism of the genes potentially can be used as a marker for the diseases.
机译:本发明涉及包括用于阿司匹林加剧的呼吸道疾病(AERD)的RAB1A基因的标志物组合物及其诊断试剂盒。更具体地,AERD诊断标志物包括用作揭示AERD进展的标志物的RAB1A基因的单核苷酸多态性(SNP)。本发明研究了RAB1A基因的单核苷酸多态性与AERD之间的关系。在逻辑回归分析中,确认在AERD组(n = 261)中内含子5的+41170 C> Gon的次要等位基因频率显着低于ATA组(n = 1016)。在线性回归分析中,证实阿司匹林耐药性存在+41170 C> G与FEV1降低之间的强烈关系(P = 0.01)。 RAB1A基因对于改善哮喘患者至关重要。基因的遗传多态性潜在地可以用作疾病的标记。

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