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Published on: November 8, 2015
Mycophenolate mofetil therapy for children with steroid-resistant nephrotic syndrome
Zhihui Li1, Cuirong Duan, Jinhua He
1Department of Nephrology, Hunan Children's Hospital, Hunan, People's Republic of China. Lizh0731@yahoo.com.cn
Insights
Mycophenolate mofetil (MMF) effectively treats steroid-resistant nephrotic syndrome (SRNS) in young children. This therapy reduced proteinuria and improved cholesterol and albumin levels in children under two years old.
Area of Science:
- Pediatric Nephrology
- Clinical Pharmacology
Background:
- Steroid-resistant nephrotic syndrome (SRNS) presents a significant therapeutic challenge in pediatric patients.
- Early-onset SRNS, particularly in children under two years, requires effective treatment strategies.
Purpose of the Study:
- To evaluate the efficacy and safety of mycophenolate mofetil (MMF) in treating steroid-resistant idiopathic nephrotic syndrome (SRINS) in children under two years of age.
- To assess the impact of MMF on proteinuria, serum albumin, and serum cholesterol levels in this pediatric cohort.
Main Methods:
- A cohort of 24 children (<2 years) with SRINS received prednisone followed by mycophenolate mofetil (MMF) at 25-30 mg/kg daily for 6-12 months.
- Prednisone dosage was gradually reduced, and biochemical parameters were monitored every two months.
Main Results:
- Complete remission was observed in 15 patients, partial remission in six, and three showed no response to MMF.
- MMF treatment led to a time-dependent decrease in urinary protein and serum cholesterol, and an increase in serum albumin.
Conclusions:
- Mycophenolate mofetil (MMF) demonstrates efficacy in reducing proteinuria in young children (<2 years) with SRINS.
- MMF therapy represents a potentially effective treatment strategy for SRINS in this vulnerable pediatric population.
Abstract:
Treating children with steroid-resistant nephrotic syndrome (SRNS) has been a clinical challenge for pediatricians. We recruited 24 children (18 boys and six girls) with steroid-resistant idiopathic nephrotic syndrome (SRINS) who were <2 years. All patients were administered prednisone 2 mg/kg per day prior to mycophenolate mofetil (MMF). By the end of the eighth week, MMF was initiated at 25-30 mg/kg daily for 6- 12 months. Prednisone dose was reduced stepwise. Biochemical assays were performed every 2 months. Complete remission was achieved in 15 patients, partial remission in six, and no response to MMF was noted in three. With MMF treatment, the levels of urinary protein and serum cholesterol decreased and that of serum albumin increased in a time-dependant manner. We demonstrated the MMF could reduce proteinuria in SRINS children <2 years. Our study suggests that MMF therapy might be an effective strategy for treating SRINS in children <2 years.
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