Related Experiment Video
Updated: Aug 19, 2026

Quantification of the Immunosuppressant Tacrolimus on Dried Blood Spots Using LC-MS/MS
Published on: November 8, 2015
Switch from cyclosporine A to mycophenolate mofetil in nephrotic children
Tim Ulinski1, Laurence Dubourg, Marie Hélène Saïd
1Department of Pediatrics, Nephrology Unit, Hôpital Edouard Herriot, 69437 Lyon Cedex 03, France.
Insights
Switching children with nephrotic syndrome from cyclosporine A (CyA) to mycophenolate mofetil (MMF) improved kidney function and allowed for steroid reduction. MMF proved safe and effective in managing both steroid-dependent and steroid-resistant nephrotic syndrome in this cohort.
Area of Science:
- Pediatric Nephrology
- Pharmacology
- Immunosuppression
Background:
- Cyclosporine A (CyA) treatment for nephrotic syndrome (NS) in children can cause nephrotoxicity, leading to decreased glomerular filtration rate (GFR).
- Steroid-dependent (SD) and steroid-resistant (SR) NS require effective immunosuppressive therapy, but long-term side effects are a concern.
Purpose of the Study:
- To evaluate the safety and efficacy of switching from CyA to mycophenolate mofetil (MMF) in pediatric patients with SD or SR NS experiencing CyA-induced nephrotoxicity.
- To assess the impact of this switch on renal function, proteinuria, and steroid requirements.
Main Methods:
- Nine children with SD or SR NS and reduced GFR under CyA were switched to MMF (1 g/1.73 m(2) twice daily).
- CyA was withdrawn, and oral steroid doses were reduced if possible.
- Patients were monitored for adverse effects, proteinuria, serum protein levels, GFR, and blood pressure.
Main Results:
- No significant adverse effects (diarrhea, hematological anomalies) were observed with MMF.
- GFR significantly increased post-switch (mean 76.9 to 119.9 mL/1.73 m(2)/min; P<0.001).
- Oral steroid doses were significantly reduced (median 0.85 to 0.29 mg/kg/d; P=0.026), with stable remission in SD NS and no significant change in proteinuria in SR NS.
Conclusions:
- Switching from CyA to MMF is a safe short-term option for children with SD/SR NS, improving kidney function and enabling steroid-sparing.
- Interruption of CyA led to rapid GFR amelioration, potentially benefiting growth, blood pressure, and physical appearance.
Abstract:
Nephrotoxicity is a well-known adverse effect of cyclosporine A (CyA) treatment in children with steroid-dependent (SD) and steroid-resistant (SR) nephrotic syndrome (NS). We analyzed nine children (age: 3.3-15.7 years, two girls) with SD or SR NS who experienced a significant decrease in their GFR under CyA treatment as measured by inulin clearance (C(IN)). Mycophenolate mofetil (MMF) was introduced progressively until doses of 1 g/1.73 m(2) twice daily were reached. CyA treatment was stopped after introduction of MMF and oral steroids were reduced if possible. After a median follow up of 261 days, no adverse effects of MMF such as diarrhea or hematological anomalies occurred in our patients. After switching from CyA to MMF, those children with SD NS remained in remission without proteinuria and those with SR NS did not show any significant changes in their residual proteinuria. The serum protein level did not change significantly in any of the children analyzed. GFR increased from a mean of 76.9+/-4.8 to 119.9+/-5.9 mL/1.73 m(2) per min (P<0.001). Oral steroid treatment could be reduced from a median [range] prednisone dose of 0.85 [0.26-2.94] mg/kg/d pre-MMF to 0.29 [0-1.1] mg/kg per day (P=0.026), and blood pressure decreased moderately after CyA withdrawal, but the difference did not reach statistical significance. We conclude that a switch from CyA to MMF seems to be safe for children with SDNS and SRNS in terms of side effects as well as disease control, at least in the short term. Interruption of CyA treatment lead to rapid amelioration of kidney function in these children, often associated with steroid sparing, which may lead to additional benefit for growth velocity, blood pressure and physical appearance.
Related Concept Videos
Pharmacokinetics in Pediatric Patients: Drug Excretion
Drugs for Treatment of Crohn's Disease in IBD Using Immunomodulatory Agents
Kidney Transplant II: Surgical Procedure
Cryptococcal Meningitis
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Drugs for Treatment of Crohn's Disease in IBD Using Glucocorticoids