首页> 外文期刊>Acta biochimica Polonica >Polymorphic variants of MIF gene and prognosis in steroid therapy in children with idiopathic nephrotic syndrome
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Polymorphic variants of MIF gene and prognosis in steroid therapy in children with idiopathic nephrotic syndrome

机译:MIF基因多态性变异与特发性肾病综合征患儿激素治疗的预后

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Nephrotic syndrome (NS) is the most common reason of proteinuria in children and can be caused by the pathology of renal glomeruli. Steroid therapy is typically used in this disorder. It has been shown that MIF is a cytokine which counteracts the immunosuppressive properties of glucocorticoids. The aim of this study was looking for a correlation between MIF polymorphisms and genetic susceptibility to steroid resistance in children with INS (Idiopathic NS). Methods: The study was performed in 71 patients with INS including SRNS (steroid resistance nephrotic syndrome) (41) and SSNS (steroid sensitive nephrotic syndrome) (30) and in 30 control subjects. We employed Sanger sequencing and capillary electrophoresis. Linkage disequilibrium was made using Haploview and PHASE. Results: We didn't observe a statistical significance between SNPs detected in patients with INS and controls. Our studies revealed statistical significance for two polymorphisms: rs2070767C>T and rs2000466T>G between patients with SRNS and SSNS. The results for rs34383331T>A are close to being statistically significant. Statistical significance was revealed for CATT5/CATT6 genotype in SRNS group vs SSNS group (OR=4.604, 95%CI=1.356-15.632, p=0.0168). We found that the frequency of 5/X-CATT genotype compared with X/X-CATT genotype was significantly higher in SRNS patients vs SSNS (OR=3.167, 95%CI=1.046-9.585, p=0.0426). In linkage disequilibrium analysis we didn't show involvement in susceptibility to INS and steroid sensitive phenotype. Conclusions: Our results suggest that the role of MIF polymorphisms in the susceptibility to positive response to steroid therapy is still unresolved. It indicates that MIF may be involved in indirect and complex molecular mechanisms of steroid activity in hormone-dependent metabolic pathways in children with INS. Because of ambiguous findings, pleiotropic features of this cytokine require that more research should be undertaken.
机译:肾病综合征(NS)是儿童蛋白尿的最常见原因,可能是由肾小球的病理引起的。类固醇疗法通常用于这种疾病。已经显示出MIF是抵消糖皮质激素的免疫抑制特性的细胞因子。这项研究的目的是寻找INS儿童(特发性NS)的MIF多态性与对类固醇抵抗的遗传易感性之间的相关性。方法:该研究在71名包括SRNS(类固醇抵抗性肾病综合征)(41)和SSNS(类固醇敏感性肾病综合征)(30)的INS患者中进行,并在30名对照受试者中进行。我们采用了Sanger测序和毛细管电泳。使用Haploview和PHASE进行连锁不平衡。结果:我们没有观察到在INS患者和对照组中检测到的SNP之间有统计学意义。我们的研究揭示了SRNS和SSNS患者之间两个多态性的统计学意义:rs2070767C> T和rs2000466T> G。 rs34383331T> A的结果接近于统计上的显着性。 SRNS组vs SSNS组的CATT5 / CATT6基因型具有统计学意义(OR = 4.604,95%CI = 1.356-15.632,p = 0.0168)。我们发现,SRNS患者中5 / X-CATT基因型的频率与X / X-CATT基因型相比,SSNS显着更高(OR = 3.167,95%CI = 1.046-9.585,p = 0.0426)。在连锁不平衡分析中,我们没有显示出对INS和类固醇敏感表型的敏感性。结论:我们的结果表明,MIF基因多态性在类固醇治疗阳性反应易感性中的作用仍未得到解决。这表明MIF可能与INS儿童激素依赖性代谢途径中类固醇活性的间接和复杂分子机制有关。由于发现的模棱两可,该细胞因子的多效性特征需要进行更多的研究。

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