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Levamisole therapy in children with frequently relapsing and steroid-dependent nephrotic syndrome: a single-center
Elżbieta Kuźma-Mroczkowska1, Piotr Skrzypczyk1, Małgorzata Pańczyk-Tomaszewska1
1Department of Pediatrics and Nephrology, Medical University of Warsaw, Poland.
Insights
Levamisole effectively reduces relapses in children with frequently relapsing and steroid-dependent nephrotic syndrome (FRNS/SDNS). However, early proteinuria relapse indicates limited benefit from continued levamisole treatment in these patients.
Area of Science:
- Pediatric Nephrology
- Immunopharmacology
- Clinical Therapeutics
Background:
- Levamisole, an immunomodulatory antihelmintic, is suggested to decrease relapses in children with frequently relapsing and steroid-dependent nephrotic syndrome (FRNS/SDNS).
- This study details a single center's experience using levamisole for FRNS/SDNS treatment.
Purpose of the Study:
- To evaluate the efficacy of levamisole in managing FRNS/SDNS in pediatric patients.
- To analyze treatment duration, relapse rates, and side effects associated with levamisole therapy.
Main Methods:
- Retrospective analysis of 53 children with FRNS/SDNS treated with levamisole for at least 6 months (1984-2011).
- Evaluation of disease course, renal biopsy, concomitant medications, prednisone dosage, levamisole duration, relapse frequency, and adverse events.
- Statistical analysis of relapse rates before and during levamisole treatment.
Main Results:
- Patients received levamisole for a mean of 15.0 ±7.3 months, with a mean prednisone dose of 1.2 ±0.6 mg/kg/24 h at initiation.
- Proteinuria relapsed in 64.2% of children, with the first relapse occurring at a mean of 8.8 ±8.1 months.
- Levamisole significantly reduced the annual relapse rate from 2.7 ±2.0 to 1.8 ±2.1 (p = 0.02), with earlier relapses correlating with higher overall relapse numbers.
Conclusions:
- Levamisole demonstrates effectiveness in reducing relapse frequency in pediatric FRNS/SDNS.
- Early relapse of proteinuria during levamisole therapy suggests a poorer response and limited benefit from its continuation.
Introduction:
Numerous studies suggest that levamisole, an antihelmintic agent with an immunomodulatory effect, reduces the number of relapses in children with frequently relapsing and steroid-dependent nephrotic syndrome (FRNS/SDNS). The aim of the study was to present a single center's experience in treatment of FRNS and SDNS with levamisole.
Material And Methods:
Among 72 children with FRNS/SDNS treated in our department with levamisole in the years 1984-2011 we studied in detail 53 patients (mean age: 6.5 ±3.0 years), in whom the medication was administered for at least 6 months. In these 53 patients we evaluated: the course of the disease before levamisole, the renal biopsy result, medications used, prednisone dose on levamisole initiation, duration of levamisole treatment, time to first relapse and number of relapses on levamisole, and levamisole side effects.
Results:
The duration of nephrotic syndrome was 3.4 ±2.9 years, and the number of relapses before levamisole treatment was 6.0 ±3.4. The dose of prednisone on initiation of levamisole treatment was 1.2 ±0.6 mg/kg/24 h, and the duration of levamisole treatment was 15.0 ±7.3 months. During levamisole treatment proteinuria relapsed in 34/53 (64.2%) children, and the time to first relapse was 8.8 ±8.1 months. During levamisole therapy relapses of the disease decreased significantly (2.7 ±2.0 vs. 1.8 ±2.1 relapses/year, p = 0.02). Time to first relapse correlated with total number of relapses (R = -0.59, p < 0.001) and number of relapses in one year during levamisole treatment (R = -0.60, p < 0.001).
Conclusions:
Levamisole is effective in reducing the number of relapses in children with frequently relapsing and steroid-dependent nephrotic syndrome. Early relapse of proteinuria on levamisole treatment in children with FRNS/SDNS suggests low efficacy of further treatment.
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