2013
DOI: 10.1373/clinchem.2013.202671
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MicroRNAs in Idiopathic Childhood Nephrotic Syndrome

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Cited by 4 publications
(4 citation statements)
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“…A set of miRNAs that was dysregulated in the kidney tissues of children with nephropathy and was related to the pathogenesis of NS in children (Lu et al, 2015). Moreover, these miRNAs were also significantly increased in the serum or urine of children with NS and markedly decreased with the clinical remission of the patients, indicating that this specific set of circulating or urinary miRNAs could serve as a promising and noninvasive means in monitoring and stratifying children with severe complications (Lorenzen & Thum, 2013; Lu et al, 2015).…”
Section: Circulating and Urinary Mirnasmentioning
confidence: 99%
“…A set of miRNAs that was dysregulated in the kidney tissues of children with nephropathy and was related to the pathogenesis of NS in children (Lu et al, 2015). Moreover, these miRNAs were also significantly increased in the serum or urine of children with NS and markedly decreased with the clinical remission of the patients, indicating that this specific set of circulating or urinary miRNAs could serve as a promising and noninvasive means in monitoring and stratifying children with severe complications (Lorenzen & Thum, 2013; Lu et al, 2015).…”
Section: Circulating and Urinary Mirnasmentioning
confidence: 99%
“…In EBioMedicine , Zhang et al explored the clinical value of urinary exosomal miRNAs in children with idiopathic nephrotic syndrome [6]. In a previous manuscript, they reported 5 miRNAs increased in the serum and 1 in the urine (miRNA-30a-5p) in children with idiopathic NS compared to controls [7,8]. In the present study, urine samples were collected in 129 children with NS and in 126 age-sex matched healthy controls.…”
mentioning
confidence: 93%
“…At present, the primary symptoms are severe proteinuria and hypoalbuminemia, as well as hyperlipidaemia and oedema, which are major clinical diagnostic indicators, but these symptoms may not be accurate predictors for patient outcome because of symptom heterogeneity and complications [5,6]. Renal biopsy, the standard method to judge pathological type and prognosis, is an invasive operation with latent risk and is normally not feasible for serial monitoring, especially in children [7,8]. Moreover, misdiagnosis may be caused by improper tissue sampling [9].…”
Section: Introductionmentioning
confidence: 99%
“…We previously found a set of miRNAs that was dysregulated in the kidney tissues of children with nephropathy and was related to the pathogenesis of nephrosis in children [11]. Moreover, these miRNAs were also significantly increased in the serum or urine of children with NS and markedly decreased with the clinical remission of the patients, indicating that this specific set of circulating or urinary miRNAs could serve as a promising and non-invasive means in monitoring and stratifying children with severe complications [7,8].…”
Section: Introductionmentioning
confidence: 99%