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From the Department of Paediatrics (Dr. Fraser, S. Whiting), Childrens Hospital of Eastern Ontario, Ottawa; Department of Anatomy and Cell Biology (Drs. Fraser and Andrew), Queens University, Kingston; Clinical Trials Group (Drs. Fraser and Cunnane, S. Whiting), Canadian Paediatric Epilepsy Network (CPEN); Department of Paediatrics (Dr. Macdonald), Queens University, Kingston; and Department of Nutritional Sciences (Dr. Cunnane, K. MusaVeloso), University of Toronto, Ontario, Canada.
Address correspondence and reprint requests to Dr. Douglas D. Fraser, Division of Critical Care Medicine, Department of Paediatrics, Childrens Hospital of Eastern Ontario, 401 Smyth Rd., Ottawa, Ontario, Canada K1H 8L2; e-mail: drfraser{at}hotmail.com
The authors analyzed blood metabolites in nine children with epilepsy prior to starting the ketogenic diet (KD) and 3 to 4 weeks after KD therapy. Elevated ß-hydroxybutyrate and cortisol levels were observed in all children on the KD. Free fatty acids increased 2.2-fold on the KD, with significant elevations in most polyunsaturated fatty acids (PUFA; arachidonate increased 1.6- to 2.9-fold and docosahexaenoate increased 1.5- to 4.0-fold). The rise in total serum arachidonate correlated with improved seizure control. Elevated PUFA may represent a key anticonvulsant mechanism of the KD.
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