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Published on: September 1, 2015
Increased cystatin C concentration in urine of nephrotic children
Marcin Tkaczyk1, Michał Nowicki, Jolanta Lukamowicz
1Department of Nephrology and Dialysis, Polish Mother's Memorial Hospital Research Institute, Łódź, Poland. mtkaczyk@uni.lodz.pl
Insights
In children with idiopathic nephrotic syndrome (INS) relapse, cystatin C was found in urine, suggesting massive proteinuria affects kidney cystatin C handling. This finding is crucial for understanding pediatric kidney disease biomarkers.
Area of Science:
- Pediatric Nephrology
- Clinical Chemistry
- Biomarker Research
Background:
- Idiopathic nephrotic syndrome (INS) is a common kidney disease in children.
- Proteinuria is a hallmark of INS, indicating kidney damage.
- Cystatin C is a potential biomarker for kidney function.
Purpose of the Study:
- To investigate urine and plasma cystatin C levels in children experiencing INS relapse.
- To compare cystatin C concentrations between children with active INS, remission, and healthy controls.
- To explore the relationship between proteinuria and renal cystatin C handling in pediatric INS.
Main Methods:
- Recruitment of three groups: children with INS relapse (proteinuria), children in INS remission, and healthy controls.
- Measurement of urine and plasma cystatin C concentrations in all participants.
- Steroid treatment was administered to children with INS.
Main Results:
- Cystatin C was detected in the urine of children with active INS and significant proteinuria.
- Differences in cystatin C levels between groups were analyzed (specific data not detailed in abstract).
- The presence of cystatin C in urine suggests altered renal handling during active disease.
Conclusions:
- Massive proteinuria in pediatric idiopathic nephrotic syndrome may significantly influence the kidney's handling of cystatin C.
- Urine cystatin C may serve as a potential indicator of active disease or renal dysfunction in INS.
- Further research is warranted to elucidate the precise role and diagnostic utility of cystatin C in pediatric nephrotic syndrome.
Abstract:
The aim of this study was to evaluate changes in urine and plasma concentrations of cystatin C in children with a relapse of the idiopathic nephrotic syndrome(INS). The study group comprised 12 children with INS with proteinuria and 12 children in an 8-week remission,both treated with steroids. Twelve healthy children served as controls. Cystatin C was detectable in the urine of children with proteinuria. The study suggests that massive proteinuria may influence renal cystatin C handling.
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