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Variables Associated with a Urinary MicroRNAs Excretion Profile Indicative of Renal Fibrosis in Fabry Disease Patients

机译:与尿RORNAS排泄曲线相关的变量,指示法布里病患者肾纤维化

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Introduction. In advanced Fabry nephropathy stages, enzyme replacement theraphy (ERT) efficacy decreases, due to its impossibility to reverse renal fibrosis. Therefore, the finding of early kidney fibrosis biomarkers in affected patients is of interest. During renal fibrosis miR-21, miR-192 and miR-433 (fibrosis promotors) are activated by transforming growth factor-β (TGF-β), and miR-29 and miR-200 family (fibrosis supressors) are inhibited by TGF-β. The aim of this study is to analyze the probability that Fabry disease (FD) patients with some clinical variables can present an urinary microRNAs excretion profile indicative of renal fibrosis through a logistic regression analysis. Results. A population of 34 participants was included: 24 FD patients and 10 controls. 16/24 (66.66%) FD patients presented microRNAs urinary excretion profile indicative of renal fibrosis. This profile was observed by decrease of fibrosis suppresors miR-29 and miR-200 and not by increase of fibrosis promotors miR-21, miR192, and miR-433. Hypohidrosis, angiokeratomas, neuropathic pain, hearing loss, cardiac involvement, male gender, reduced αGalA activity, and renin-angiotensin-aldosterone system inhibitors treatment are associated with the appearance of amicroRNAs urinary excretion profile indicative of renal fibrosis. A probable beneficial effect on urinary microRNAs excretion profile was observed in patients receiving ERT with agalsidase beta. The correlation between parameters of renal function with each family of microRNAs was studied. The only association with statistical significance was found between miR-21 and urine albumin-creatinine ratio (p =0.021). Conclusions. A probable microRNAs regulation not mediated by TGF-β should be considered or TGF-β has a different effect in FD than in other nephropathies on microRNAs regulation. Typical clinical manifestations of classic FD are associated with appearance of urinary microRNAs profile indicative of renal fibrosis. FD patients express renal fibrosis biomarkers in urine prior to onset of pathological albuminuria. A direct correlation between urinary miR-21 and degree of albuminuria was observed.
机译:介绍。在先进的法布里肾病阶段,由于其不可能逆转肾纤维化,酶替代酶替代(ert)效力降低。因此,在受影响患者中发现早期肾纤维化生物标志物感兴趣。在肾纤维化中,通过转化生长因子-β(TGF-β)激活miR-21,miR-192和miR-433(纤维化启动器),并且通过TGF抑制miR-29和miR-200系列(纤维化素) β本研究的目的是分析法布里疾病(FD)患者一些临床变量的概率可以在逻辑回归分析通过逻辑回归分析呈现尿稻纤维化的尿RORNA排泄曲线。结果。包括34名参与者的人口:24例FD患者和10名对照。 16/24(66.66%)FD患者呈现MicroRNAS尿液排泄曲线,指示肾纤维化。通过纤维化贮存器miR-29和miR-200的减少观察到该概况,而不是通过纤维化启动剂MiR-21,MiR192和MiR-433的增加而不是增加。 Hypohidrosis,血管疗法,神经性疼痛,听力损失,心脏受累,男性性别,降低αgala活性,肾血管素 - 醛固酮系统抑制剂治疗与表明肾纤维化的Amicrornas尿排泄谱的外观有关。在接受与羟基苯胺酶β接受ert的患者中观察到对尿瘤排泄曲线的可能有益效果。研究了每个Micrornas肾功能参数之间的相关性。在miR-21和尿白蛋白 - 肌酐比率之间发现了唯一的统计显着性的关联(p = 0.021)。结论。不应考虑未被TGF-β介导的可能的微小RNA调节,或者TGF-β在FD中具有不同的效果,而不是在MicroRNA调节上的其他肾病。经典FD的典型临床表现与指示肾纤维化的尿瘤谱的外观相关。 FD患者在病理蛋白酶发作前表达尿液中的肾纤维化生物标志物。观察到尿miR-21与白蛋白尿道度之间的直接相关性。

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