The Ketogenic Diet in Children with Glut1 Deficiency Syndrome and Epilepsy - 07/03/14
Doi : 10.1016/j.jpeds.2008.05.012
Markus Rauchenzauner, MD a, ⁎ 
, Jörg Klepper, MD, PD b, c, Bärbel Leiendecker c, Gerhard Luef, MD d : Professor, Kevin Rostasy, MD, PD a, Christoph Ebenbichler, MD e : Professor
, Jörg Klepper, MD, PD b, c, Bärbel Leiendecker c, Gerhard Luef, MD d : Professor, Kevin Rostasy, MD, PD a, Christoph Ebenbichler, MD e : Professor a Department of Pediatrics IV, Division of Neuropediatrics, University Hospital Innsbruck, Austria
b Department of Pediatrics, Hospital Aschaffenburg, Aschaffenburg, Germany
c Department of Pediatrics, University Hospital Essen, Germany
d Department of Neurology, Epilepsy Unit, University Hospital Innsbruck, Austria
e Department of Internal Medicine, University Hospital Innsbruck, Austria
Reprint requests: Dr. Markus Rauchenzauner, Department of Pediatrics IV, Division of Neuropediatrics, Medical University Innsbruck, Anichstrasse 35, 6020 Innsbruck, AustriaRésumé |
The effects of a long-term ketogenic diet in children with Glut1 deficiency syndrome on metabolism are unknown. Our results indicate a characteristic effect of a long-term ketogenic diet on glucose and lipid homeostasis in Glut1 deficiency syndrome. Although serum lipids and apolipoproteins reflect a proatherogenic lipoprotein profile, adipocytokine constellation is not indicative of enhanced cardiovascular risk.
Le texte complet de cet article est disponible en PDF.Abbreviations : Apo, Glut1DS, HOMA-IR, KD, sOB-R
Plan
| The authors report no conflicts of interest. |
© 2008
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Vol 153 - N° 5
P. 716-718 - novembre 2008 Retour au numéro
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