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首页> 外文期刊>Journal of clinical laboratory analysis. >The association of NLRP3 and TNFRSF1A polymorphisms with risk of ankylosing spondylitis and treatment efficacy of etanercept
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The association of NLRP3 and TNFRSF1A polymorphisms with risk of ankylosing spondylitis and treatment efficacy of etanercept

机译:NLRP3和TNFRSF1A多态性与强直性脊柱炎风险和依那西普治疗效果的关系

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BackgroundTo discover how NLRP3 and TNFRSF1A polymorphisms affect the efficacy of traditional medicine and etanercept for ankylosing spondylitis (AS) patients. MethodsSingle nucleotide polymorphism (SNP) and haplotype analyses were conducted based on determined NLRP3 and TNFRSF1A among AS patients. We subsequently analyzed the relationship between relevant clinical indexes and polymorphisms of NLRP3 and TNFRSF1A . ResultsThe 4 SNP loci on NLRP3 and 3 SNP loci on TNFRSF1A showed significant linkage disequilibrium, respectively. The T allele of NLRP3 rs4612666 and the T allele of TFRSF1A rs4149570 are both associated with AS ( P Conclusion NLRP3 and TFRSF1A (rs4149570) are associated with AS susceptibility. There is a significant association between NLRP3 polymorphisms and treatment of etanercept.
机译:背景为了发现NLRP3和TNFRSF1A多态性如何影响传统药物和依那西普对强直性脊柱炎(AS)患者的疗效。方法根据测定的AS患者NLRP3和TNFRSF1A进行单核苷酸多态性(SNP)和单倍型分析。随后我们分析了相关临床指标与NLRP3和TNFRSF1A基因多态性的关系。结果NLRP3上的4个SNP基因座和TNFRSF1A上的3个SNP基因座分别显示出显着的连锁不平衡。 NLRP3 rs4612666的T等位基因和TFRSF1A rs4149570的T等位基因均与AS相关(P结论NLRP3和TFRSF1A(rs4149570)与AS易感性有关。NLRP3多态性与依那西普治疗之间存在显着关联。

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