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The Effect of Long-term Steroid Therapy on Linear Growth of Nephrotic Children
Abbas Madani1, Sham-Una Umar, Rambod Taghaodi
1Department of Pediatrics, Tehran University of Medical Sciences, Tehran, Iran ; Children's Medical Center, Pediatrics Center of Excellence, Tehran, Iran.
Insights
Steroid treatment for nephrotic syndrome in children did not show significant growth retardation overall. While some children experienced growth issues, the group as a whole maintained normal growth trajectories during long-term follow-up.
Area of Science:
- Pediatric Nephrology
- Endocrinology
- Growth and Development
Background:
- Steroids are the primary treatment for nephrotic syndrome (NS) in children.
- Concerns exist regarding steroid-induced growth impairment, with conflicting evidence in clinical studies.
Purpose of the Study:
- To evaluate the long-term effects of prednisolone on linear growth in children with nephrotic syndrome.
- To analyze factors influencing growth outcomes in this pediatric population.
Main Methods:
- Retrospective review of hospital records for 147 children with NS treated with prednisolone for at least five years.
- Analysis of height standard deviation scores (SDS), prednisolone dosage and duration, biopsy findings, and use of steroid-sparing agents (SSA).
Main Results:
- The overall study population showed no significant change in height SDS (Ht(SDS)) over the follow-up period.
- Two subgroups emerged: 62 children showed growth improvement (initial Ht(SDS) -1.63 to final Ht(SDS) -0.08), while 85 experienced growth retardation (initial Ht(SDS) -0.13 to final Ht(SDS) -1.59).
Conclusions:
- Long-term prednisolone treatment, following ISKDC guidelines, did not result in statistically significant linear growth retardation for the overall group of children with nephrotic syndrome.
- Individual growth responses varied, with a notable proportion experiencing growth retardation despite no significant difference compared to those with improved growth.
Objective:
Steroids are still the mainstay of management of nephrotic syndrome (NS). It was shown that steroids could impair growth and development of children. However, other clinical studies have shown conflicting results.
Methods:
Hospital records of 147 children with diagnosis of NS who were followed during 1988-2008 are reviewed relating to height measurements. All patients were treated with prednisolone and had been followed for at least five years. Height measures were transformed into standard deviation score (SDS). Information on dose and duration of prednisolone therapy, histological findings of biopsy as well as concomitant use of steroid-sparing agents (SSA) were also analyzed.
Findings:
Mean age at onset of NS was 5.94 years and at last follow-up visit 15.08 years. All patients had normal renal function during entire duration of the study. Analysis of the whole population did not show any significant alterations in the height SDS (Ht(SDS)) between the first and the last follow-up visit (P=0.5; -0.76±2.0 vs. -0.89±2.05 respectively). The patients were divided into two subgroups. Subgroup A, which achieved growth improvement, was composed of 62 children (initial Ht(SDS) -1.63; final Ht(SDS) -0.08; P<0.001) and subgroup B, that showed growth retardation, included 85 children (initial Ht(SDS) -0.13; final Ht(SDS) -1.59; P<0.001).
Conclusion:
No statistically significant retardation of linear growth was observed in the study population as a group following treatment with prednisolone according to the guidelines of ISKDC. Although about 62 subjects had growth retardation, children treated with prednisolone were not different from those who had increased growth.
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