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Carnitine Deficiency in Chinese Children with Epilepsy on Valproate Monotherapy
Li Qiliang1, Song Wenqi2, Jin Hong3
1Departments of Medical Laboratory, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.
Insights
Secondary carnitine deficiency affects over 20% of Chinese children with epilepsy on valproate. Female gender, elevated liver enzymes, and 1-12 months of valproate treatment are key risk factors.
Area of Science:
- Biochemistry
- Pediatric Neurology
- Clinical Pharmacology
Background:
- Epilepsy is a common neurological disorder in children.
- Valproate is a widely used antiepileptic drug.
- Secondary carnitine deficiency is a potential adverse effect of valproate therapy.
Purpose of the Study:
- To determine the incidence of secondary carnitine deficiency in Chinese children with epilepsy on valproate monotherapy.
- To identify independent risk factors associated with this deficiency.
Main Methods:
- A comparative study involving 299 children with epilepsy on valproate monotherapy and 299 age- and sex-matched healthy controls.
- Measurement of free carnitine and acylcarnitines levels.
- Statistical analysis to identify independent risk factors.
Main Results:
- Children on valproate showed significantly lower free carnitine levels compared to controls (23.86 vs. 36.37 µmol/L).
- Carnitine deficiency was observed in 21.1% of children on valproate, with most cases being asymptomatic.
- Independent risk factors identified were female gender (OR 2.1), high alanine aminotransferase levels (OR 1.0), and duration of valproate treatment between 1-12 months (OR 1.9).
Conclusions:
- Secondary carnitine deficiency is prevalent in Chinese children with epilepsy treated with valproate.
- Female patients, those with elevated liver enzymes, and those treated for 1-12 months are at higher risk.
Objective:
To explore the incidence and independent risk-factors of secondary carnitine deficiency in Chinese children with epilepsy on valproate monotherapy.
Methods:
The free carnitine and acylcarnitines levels in 299 children with epilepsy on valproate monotherapy between June 2014 and September 2015 were compared with age- and sex-matched 299 healthy controls.
Results:
Children with valproate monotherapy had lower free carnitine levels [23.86 (10.60) µmol/L] than the controls [36.37 (9.37) µmol/L] (P<0.01). Most acylcarnitines were significantly lower in children with valproate monotherapy than controls. 63 children (21.1%) with epilepsy had carnitine deficiency; 54 were asymptomatic. Female gender (OR 2.1), high alanine aminotransferase levels (OR 1.0) and long duration of VPA treatment (1-12 mo) (OR 1.9) were independent risk factors for secondary carnitine deficiency induced by VPA.
Conclusion:
Carnitine deficiency with valproate is more likely in females, those with transaminitis, and those receiving the drug for 1-12 months.
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