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Treatment of idiopathic nephrotic syndrome with levamisole
Insights
Levamisole treatment showed benefits for children with frequently relapsing idiopathic nephrotic syndrome (INS), allowing for reduced corticosteroid use in some patients. This immunomodulatory drug may be effective for INS with few side effects.
Area of Science:
- Pediatric Nephrology
- Immunology
- Pharmacology
Background:
- Idiopathic nephrotic syndrome (INS) is a significant kidney disorder in children.
- Frequently relapsing INS often requires long-term immunosuppressive therapy, including corticosteroids.
- Corticosteroid therapy is associated with numerous adverse effects.
Purpose of the Study:
- To evaluate the efficacy and safety of levamisole in children with frequently relapsing idiopathic nephrotic syndrome.
- To determine if levamisole can reduce the need for corticosteroid therapy in this patient population.
Main Methods:
- A prospective study involving 30 children with frequently relapsing INS.
- Treatment with levamisole at a dose of 2.5 mg/kg body weight twice weekly for a mean duration of 9.9 months.
- Monitoring for relapses, corticosteroid dosage adjustments, and adverse events, including neutrophil counts.
Main Results:
- Levamisole was effective in 16 out of 30 children, enabling significant corticosteroid reduction without relapses.
- The drug was ineffective in 14 patients.
- Patients who responded to levamisole were older at INS onset (mean 5.8 years vs. 2.8 years).
- Neutrophil counts decreased in 7 responders, with transient granulocytopenia observed in 3 patients.
Conclusions:
- Levamisole may be an effective treatment option for children with frequently relapsing idiopathic nephrotic syndrome.
- The use of levamisole in this context appears to be associated with minimal side effects.
- Further research is warranted to confirm these findings and elucidate the mechanism of action.
Abstract:
Thirty children with frequently relapsing idiopathic nephrotic syndrome (INS) were treated with levamisole (2.5 mg/kg BW) twice a week for a mean period of 9.9 months. A beneficial effect was observed in 16 children in whom corticosteroids could be significantly decreased without relapse. Levamisole was ineffective in 14 patients. There was no difference between the two groups in the duration of INS, the number of relapses and the duration of treatment with levamisole. The mean age at onset of INS was higher in the group of patients where levamisole was effective (5.8 years versus 2.8 years). In 7 patients who responded to levamisole neutrophils decreased below 4 X 10(9)/l. Transient granulocytopenia was observed in 3. It is concluded that levamisole may be effective in frequently relapsing INS with minimal side effects.
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