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Comparison of pulse and oral steroid in childhood membranoproliferative glomerulonephritis
Elif Bahat1, Bahar Kilicarslan Akkaya, Sema Akman
1Department of Pediatric Nephrology, Karadeniz Technical University, Trabzon, Turkey. elifbahat@yahoo.com
Insights
Pulse methylprednisolone (MP) therapy shows better long-term kidney survival in children with membranoproliferative glomerulonephritis (MPGN) compared to oral prednisolone (P). Chronic kidney damage and lack of remission predict poor outcomes.
Area of Science:
- Pediatric Nephrology
- Glomerular Diseases
- Pharmacotherapy
Background:
- Childhood membranoproliferative glomerulonephritis (MPGN) lacks controlled studies comparing pulse versus oral steroid efficacy.
- Long-term renal outcomes for MPGN treatment remain an area of investigation.
Purpose of the Study:
- To compare the efficacy of pulse methylprednisolone (MP) versus oral prednisolone (P) therapy in pediatric MPGN.
- To evaluate long-term renal outcomes in children with MPGN treated with different steroid regimens.
Main Methods:
- A comparative study of 19 children with idiopathic MPGN.
- Treatment groups: 11 patients received pulse MP, 8 patients received oral P.
- Follow-up duration ranged from 4 to 124 months.
Main Results:
- Pulse MP group had significantly lower progression to end-stage renal failure (ESRF) compared to oral P group (1/11 vs. 4/8, p=0.041).
- Long-term renal survival analysis (≥8 years follow-up) also favored pulse MP (1/7 vs. 4/5, p=0.039).
- Chronic damage on initial biopsy and lack of nephrotic syndrome remission were associated with adverse renal outcomes (p=0.02, p=0.006).
Conclusions:
- Pulse MP therapy may offer superior renal function preservation in pediatric MPGN compared to oral P.
- No increased steroid-related side effects were noted with pulse MP.
- Predictive factors for poor renal outcome include chronic damage on biopsy and absence of nephrotic syndrome remission.
Background:
There has been no controlled study comparing efficacy of pulse versus oral steroid therapy in childhood membranoproliferative glomerulonephritis (MPGN). This study aimed to compare these therapies and renal outcome over a long-term period for MPGN.
Methods:
Outcome measures in 11 patients with MPGN treated with pulse methylprednisolone (MP) were compared with 8 patients with MPGN treated with oral prednisolone (P).
Results:
Nineteen children with idiopathic MPGN (mean age 9.75 years, range 3.7-14 years) were followed for a mean period of 68.21 months (range 4-124 months). Both treatment groups were similar in demographic, clinical, laboratory and histopathological characteristics on presentation. In the pulse MP group, only 1 patient out of 11 progressed to end-stage renal failure (ESRF), compared with 4 patients out of 8 in the oral P group (p=0.041). For long-term renal survival, those patients with more than 8 years of follow-up were further evaluated. Twelve patients had completed 8 years of follow-up; in the pulse MP group, 1 of 7 patients, compared with 4 of 5 patients in the oral P group progressed to ESRF (p=0.039). Chronic damage in the presentation biopsy and lack of remission in patients with nephrotic syndrome (NS) were positively associated with adverse renal outcome (p=0.02, p=0.006, respectively).
Conclusions:
Pulse MP therapy may be superior to oral P therapy in children with MPGN in preserving renal function without any increase in steroid-related side effects. Chronic damage in the presentation biopsy and lack of remission of NS are adverse features.
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