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Carnitine deficiency: Risk factors and incidence in children with epilepsy
Mitsumasa Fukuda1, Mika Kawabe1, Makoto Takehara1
1Department of Pediatrics, Ehime University Graduate School of Medicine, Toon, Ehime, Japan.
Insights
Carnitine deficiency is common in children with epilepsy, linked to tube feeding with special formulas and multiple antiepileptic drugs (AEDs). A new formula estimates carnitine levels without blood tests, aiding treatment decisions.
Area of Science:
- Pediatric Neurology
- Clinical Chemistry
- Nutritional Science
Background:
- Carnitine deficiency is prevalent in pediatric epilepsy.
- Risk factors include specific antiepileptic drugs (AEDs), feeding methods, and developmental status.
- Limited research exists on individual risk factor correlations in children with epilepsy.
Purpose of the Study:
- To investigate the influence of specific risk factors on carnitine deficiency in children with epilepsy.
- To develop a predictive formula for plasma free carnitine concentration in this population.
Main Methods:
- Enrolled 65 children with epilepsy and 26 age-matched controls.
- Measured plasma carnitine concentrations using an enzyme cycling assay.
- Correlated carnitine levels with clinical characteristics including AED use, body weight, and feeding methods.
Main Results:
- Carnitine deficiency was observed in 17% of children with epilepsy.
- Significant associations were found with tube feeding of carnitine-free formula, number of AEDs, body weight, and GMFCS score.
- A predictive formula (R²=0.504) was developed: 42.44 + 0.14×(BW) - 18.16×(feeding) - 3.19×(AEDs).
Conclusions:
- Carnitine-free tube feeding, multiple AEDs, and low body weight are key risk factors for carnitine deficiency in epileptic children.
- l-carnitine supplementation is recommended for at-risk children.
- The developed formula allows for non-invasive estimation of carnitine levels to guide treatment.
Background:
Carnitine deficiency is relatively common in epilepsy; risk factors reportedly include combination antiepileptic drug (AED) therapy with valproic acid (VPA), young age, intellectual disability, diet and enteral or parenteral feeding. Few studies have examined the correlation between each risk factor and carnitine deficiency in children with epilepsy. We examined the influence of these risk factors on carnitine deficiency, and identified a formula to estimate plasma free carnitine concentration in children with epilepsy.
Methods:
Sixty-five children with epilepsy and 26 age-matched controls were enrolled. Plasma carnitine concentrations were measured using an enzyme cycling assay, and correlations were sought with patients' other clinical characteristics.
Results:
Carnitine deficiency was found in approximately 17% of patients with epilepsy and was significantly associated with carnitine-free enteral formula only by tube feeding, number of AEDs taken (independent of VPA use), body weight (BW), body height and Gross Motor Function Classification System (GMFCS) score. Stepwise multiple linear regression analysis indicated that carnitine concentration (in μmol/L) could be accurately estimated from a formula that does not require blood testing: 42.44+0.14×(BW in kg)-18.16×(feeding)-3.19×(number of AEDs), where feeding was allocated a score of 1 for carnitine-free enteral formula only by tube feeding and 0 for taking food orally (R(2)=0.504, P<0.001).
Conclusions:
Carnitine-free enteral formula only by tube feeding, multiple AED treatment and low BW are risk factors for carnitine deficiency in children with epilepsy. l-carnitine should be administered to children at risk of deficiency to avoid complications. Treatment decisions can be informed using an estimation formula that does not require blood tests.
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