The risk of asymptomatic hyperammonemia in children with idiopathic epilepsy treated with valproate: Relationship to blood carnitine status

被引:33
作者
Hamed, Sherifa A. [1 ,3 ]
Abdella, Mostafa M. [2 ]
机构
[1] Assiut Univ Hosp, Dept Neurol, Assiut, Egypt
[2] Assiut Univ, Fac Med, Dept Pharmacol, Assiut, Egypt
[3] Childrens Natl Med Ctr, Med Genet Res Ctr, Washington, DC 20010 USA
关键词
Epilepsy; Antiepileptic drugs; Valproate; Ammonia; Carnitine; MAGNETIC-RESONANCE-SPECTROSCOPY; ISOLATED RAT HEPATOCYTES; SODIUM VALPROATE; ACID-METABOLISM; DEFICIENCY; ENCEPHALOPATHY; THERAPY; HEPATOTOXICITY; SUPPLEMENTATION; INSUFFICIENCY;
D O I
10.1016/j.eplepsyres.2009.04.002
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: Valproate (VPA) administration may be associated with adverse metabolic effects, among is hyperammonemia, which could suggest metabolic abnormalities as carnitine deficiency. This study aimed to evaluate the risk frequency of hyperammonemia and abnormal carnitine levels in children receiving VPA who were otherwise free of neurological or obvious nutritional problems. Methods: Ammonia levels were prospectively evaluated in 60 epileptic children with primary epilepsy free of neurological or nutritional problems and were treated with VPA for at least 1 year. Forty healthy children were included as controls. Ammonia levels were correlated with total carnitine (TC), free carnitine (FC), acylcarnitine (AC) and AC/FC ratio. The abnormal ammonia and carnitine levels were also re-checked after 3 months treatment with L-carnitine. Results: Compared to pre-treatment and control levels, the mean TC and FC were tower (p < 0.001) white ammonia (p < 0.01), AC (p < 0.05) and AC/FC ratio (p < 0.01) were higher. In the treated group of epileptics, TC and FC were negatively associated with ammonia (r = -0.896, p < 0.0001; r = -0.9352 p < 0.0001). Significant associations were found between FC and AC/FC levels and patient's age (FC; r = 0.4572 p < 0.05, AC/FC; r = -0.435, p < 0.05) and dose of VPA (FC; r = -0.753, p < 0.001, AC/FC; r = 0.591, p < 0.01). Ammonia was correlated with patients' age (r = -0.532, p < 0.01) and dose of VPA (r = 0.673, p < 0.01). The abnormal ammonia and carnitine levels were returned to normal after L-carnitine supplementation. Conclusions: Epileptic children treated with VPA and free of neurological disabilities are at risk for hyperammonemia that may be associated with hypocarnitinemia. Patients wilt benefit from early recognition and preventive measures as carnitine supplementation. (C) 2009 Elsevier B.V. All rights reserved.
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收藏
页码:32 / 41
页数:10
相关论文
共 53 条
[11]  
Chung Sajun, 1997, Journal of Korean Medical Science, V12, P553
[12]  
Commission on Classification and Terminology of the International League Against Epilepsy, 1989, EPILEPSIA, V30, P3890
[13]   ACTION OF THE ANTI-EPILEPTIC DRUG, VALPROIC ACID, ON FATTY-ACID OXIDATION IN ISOLATED RAT HEPATOCYTES [J].
COUDE, FX ;
GRIMBER, G ;
PELET, A ;
BENOIT, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1983, 115 (02) :730-736
[14]  
De Vivo D., 1990, Int Pediatr, V5, P134
[15]  
De Vivo DC, 1998, EPILEPSIA, V39, P1216
[16]   Valproate-induced hyperammonaemic encephalopathy: review of 14 cases in the psychiatric setting [J].
Dealberto, Marie-Jose C. C. .
INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, 2007, 22 (06) :330-337
[17]   PROPIONYLCARNITINE EXCRETION IN PROPIONIC AND METHYLMALONIC ACIDURIAS - A CAUSE OF CARNITINE DEFICIENCY [J].
DIDONATO, S ;
RIMOLDI, M ;
GARAVAGLIA, B ;
UZIEL, G .
CLINICA CHIMICA ACTA, 1984, 139 (01) :13-21
[18]   SLOW REPLENISHMENT OF CARNITINE DEFICIENCY AFTER CESSATION OF LONG-TERM TREATMENT WITH PIVALOYL-CONTAINING ANTIBIOTICS [J].
DIEP, QN ;
BOHMER, T ;
HOLME, JI ;
TORVIK, A ;
STORROSTEN, OT ;
LOENNECKEN, CW ;
MONSTAD, P ;
JELLUM, E .
PHARMACY WORLD & SCIENCE, 1993, 15 (05) :225-229
[19]   Acute valproate poisoning - Pharmacokinetics, alteration in fatty acid metabolism, and changes during therapy [J].
Eyer, F ;
Felgenhauer, N ;
Gempel, K ;
Steimer, W ;
Gerbitz, KD ;
Zilker, T .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2005, 25 (04) :376-380
[20]   Inhibition of carnitine biosynthesis by valproic acid in rats - The biochemical mechanism of inhibition [J].
Farkas, V ;
Bock, I ;
Cseko, J ;
Sandor, A .
BIOCHEMICAL PHARMACOLOGY, 1996, 52 (09) :1429-1433