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Published on: January 18, 2019
Prednisone versus placebo in membranoproliferative glomerulonephritis: long-term clinicopathological correlations
Insights
Prednisone may slow kidney failure in children with primary membranoproliferative glomerulonephritis (MPGN). This study found no end-stage renal disease (ESRD) in the prednisone group, suggesting a potential therapeutic benefit.
Area of Science:
- Nephrology
- Pediatric Nephrology
- Immunopathology
Background:
- Primary membranoproliferative glomerulonephritis (MPGN) is a significant cause of kidney disease in children.
- Current treatment options for pediatric MPGN have varying efficacy and potential side effects.
Purpose of the Study:
- To evaluate the efficacy of prednisone in treating primary MPGN in children.
- To assess the impact of prednisone on disease progression, specifically end-stage renal disease (ESRD).
Main Methods:
- A double-blind, controlled study involving 18 children with primary MPGN.
- Patients were randomized to receive either prednisone or lactose (placebo).
- Renal biopsies and immunopathological studies were conducted at baseline, 3 years, and 5 years.
Main Results:
- None of the children treated with prednisone developed ESRD, compared to four in the control group.
- Remission rates were low in both groups (one in the prednisone group, two in the control group).
- Serial biopsies showed improvements in some immunopathological markers in both groups, but tubulointerstitial alterations and glomerulosclerosis increased generally, except in patients with proteinuria remission.
Conclusions:
- Prednisone therapy may potentially retard the progression to ESRD in children with primary MPGN.
- Further long-term studies with larger cohorts are required to definitively establish the utility of prednisone for MPGN in children.
Abstract:
Eighteen children with primary MPGN were included in a double blind controlled study. Experimental group received prednisone and control group received lactose. Studies of renal biopsy on admission, at 3 yr (17 pt) and 5 yr (8 pt) were performed. Mean time of observation in both groups was similar (6.5 yr). Four patients of the control group developed ESRD and none of the experimental group. Two patients of the control and one of the experimental group remitted. Serial immunopathological studies showed decreasing mesangial cellularity, thickening of the capillary walls and deposits in both groups. Increase tubulointerstitial alterations and percentage of global sclerotic glomeruli was generally observed except in cases in whom proteinuria disappeared. Our results suggest that prednisone therapy may retard the development of ESRD in children with MPGN. However, longer periods of observation and greater number of cases are necessary to confirm if this treatment in useful.
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