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Does nephrotoxicity exist in pediatric epileptic patients on valproate or carbamazepine therapy?
Cengiz Havali1, Kıvılcım Gücüyener2, Necla Buyan3
1Department of Pediatric Neurology, Gazi University Faculty of Medicine, Ankara, Turkey cengizhavali@gmail.com.
Insights
Valproate and carbamazepine may cause glomerular hyperfiltration in children with epilepsy. Valproate, but not carbamazepine, also showed adverse effects on renal tubular function.
Area of Science:
- Pediatric Nephrology
- Clinical Pharmacology
Background:
- Epilepsy is a common neurological disorder in children.
- Valproate and carbamazepine are frequently prescribed antiepileptic drugs.
- Potential renal side effects of these medications require investigation.
Purpose of the Study:
- To evaluate the impact of valproate and carbamazepine on renal glomerular and tubular functions in children with new-onset epilepsy.
- To compare renal function markers between patients treated with valproate, carbamazepine, and healthy controls.
Main Methods:
- Prospective study involving 54 children with new-onset epilepsy and 26 healthy controls.
- Measurement of serum creatinine, cystatin C, and urinary N-acetyl-β-d-glucosaminidase (NAG) excretion.
- Estimation of glomerular filtration rate (GFR) and calculation of urinary NAG/creatinine ratio.
Main Results:
- No significant differences in serum creatinine or cystatin C between patients and controls.
- Glomerular filtration rate (GFR) was higher in both valproate and carbamazepine groups compared to controls, suggesting glomerular hyperfiltration.
- Urinary NAG/creatinine levels were significantly elevated only in the valproate group, indicating tubular dysfunction.
Conclusions:
- Both valproate and carbamazepine may induce glomerular hyperfiltration and potential glomerular toxicity in pediatric epilepsy patients.
- Valproate demonstrates a specific adverse effect on renal tubular function, evidenced by increased urinary NAG excretion.
- Further monitoring of renal function is recommended for children treated with these antiepileptic drugs, particularly valproate.
Abstract:
The aim of this study was to investigate the effects of valproate and carbamazepine, on renal glomerular and tubular functions. The patient group comprised 54 children with new-onset epilepsy treated with valproate (n = 30) and carbamazepine (n = 24). Twenty-six healthy children were in the control group. The serum creatinine and cystatin C levels and urinary excretion of N-acetyl-β-d-glucosaminidase (NAG) levels were measured and the glomerular filtration rate (GFR) was estimated. Serum creatinine and cystatin C concentrations were not different between patients and controls. The glomerular filtration rate of the patient groups were higher than those of the control group. Thus, both drugs probably lead to glomerular hyperfiltration and toxicity for glomerular functions. However, urinary N-acetyl-β-d-glucosaminidase/creatinine levels were significantly higher in patients receiving only valproate (6.1 ± 5). The difference between carbamazepine and control groups was not significant for urinary N-acetyl-β-d-glucosaminidase/creatinine levels. Our data suggest that valproate has adverse effects on renal tubular functions.
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