Home > Journals > Medicine > Epileptic Disorders > summary
 
      Advanced search    Shopping cart    French version 
 
Latest books
Catalogue/Search
Collections
All journals
Medicine
Epileptic Disorders
- Current issue
- Archives
- Subscribe
- Order an issue
- More information
Biology and research
Public health
Agronomy and biotech.
My account
Forgotten password?
Online account   activation
Subscribe
Licences IP
- Instructions for use
- Estimate request form
- Licence agreement
Order an issue
Pay-per-view articles
Newsletters
How can I publish?
Journals
Books
Help for advertisers
Foreign rights
Book sales agents



 

Texte intégral de l'article
 
Printable version

Analysis of acylcarnitine levels by tandem mass spectrometry in epileptic children receiving valproate and oxcarbazepine


Epileptic Disorders. Volume 13, Number 4, 394-400, December 2011, Original articles

Full Text  

Author(s) : Ali Cansu, Ayse Serdaroglu, Gursel Biberoglu, Leyla Tumer, Tugba Luleci Hirfanoglu, Fatih Suheyl Ezgu, Alev Hasanoglu

Summary : This prospective study was designed to investigate whether or not monotherapy with sodium valproate (VPA) or oxcarbazepine (OXC) affects plasma levels of fatty acylcarnitine esters in children with epilepsy. A total of 56 children with idiopathic partial or generalised epilepsy were included in the study. Patients were assigned to receive either VPA or OXC monotherapy. Free carnitine (C0) and acylcarnitine profiles of the patients were investigated using tandem mass spectrometry at baseline and at six and 18 months after commencement of therapy. For patients receiving VPA or OXC monotherapy, there were no significant differences in plasma levels of C0, compared with baseline, at six and 18 months ( p>0.05). Treatment with VPA for six and 18 months correlated with a significant increase in 3-hydroxy-isovalerylcarnitine (C5-OH) (six months: +23%\; 18 months: +73%), and significant decreases in the following acylcarnitines: C6-acylcarnitine (six months: -60%\; 18 months: -66%), C14-acylcarnitine (six months: -25%\; 18 months: -38%), C16-acylcarnitine (six months: -73%\; 18 months: -73%), and C18:1-OH-acylcarnitine (six months: -60%\; 18 months: -70%), compared with baseline ( p<\;0.05). In patients receiving OXC monotherapy, on the other hand, plasma concentrations (μmol/L) of acylcarnitines (from C2 to C18:1-OH) fell within the normal reference range. The results of this study indicate that there are significant biochemical changes in acylcarnitines in ambulatory children on VPA monotherapy but these are not clinically significant. OXC monotherapy had no effect on acylcarnitine metabolism in ambulatory children.

Keywords : acylcarnitine, children, epilepsy, valproate, oxcarbazepine

 

About us - Contact us - Conditions of use - Secure payment
Latest news - Conferences
Copyright © 2007 John Libbey Eurotext - All rights reserved
[ Legal information - Powered by Dolomède ]