The Role of Carnitine Supplementation during Valproic Acid Therapy

2000 ◽  
Vol 34 (5) ◽  
pp. 630-638 ◽  
Author(s):  
Jackie Y Raskind ◽  
Gladys M El-Chaar

OBJECTIVE: To review the pathophysiology and significance of valproic acid–induced carnitine deficiency; to present and evaluate the literature pertaining to carnitine supplementation in pediatric patients receiving valproic acid; and to present the consensus guidelines for carnitine supplementation during valproic acid therapy. DATA SOURCES: A MEDLINE search (1966–December 1998) restricted to English-language literature, using MeSH headings of carnitine and valproic acid, was conducted to identify clinically relevant articles. Selected articles and references focusing on the pediatric population were included for review. DATA EXTRACTION: Study design, patient population, methods, and clinical outcomes were evaluated. DATA SYNTHESIS: Valproic acid, a widely used antiepileptic agent in the pediatric population, is limited by a 1/800 incidence of fatal hepatotoxicity in children under the age of two years. Carnitine is an essential amino acid necessary in β-oxidation of fatty acids and energy production in cellular mitochondria. It has been hypothesized that valproic acid may induce a carnitine deficiency in children and cause nonspecific symptoms of deficiency, hepatotoxicity, and hyperammonemia. Relevant published case reports and trials studying this relationship are evaluated, and a consensus statement by the Pediatric Neurology Advisory Committee is reviewed. CONCLUSIONS: Despite the lack of prospective, randomized clinical trials documenting efficacy of carnitine supplementation in preventing valproic acid–induced hepatotoxicity, the few limited studies available have shown carnitine supplementation to result in subjective and objective improvements along with increases in carnitine serum concentrations in patients receiving valproic acid. The Pediatric Neurology Advisory Committee in 1996 provided more concrete indications on the role of carnitine in valproic acid therapy, such as valproic acid overdose and valproic acid–induced hepatotoxicity. Carnitine was strongly recommended for children at risk of developing a carnitine deficiency. Although carnitine has been well tolerated, future studies are needed to evaluate the efficacy of prophylactic carnitine supplementation for the prevention of hepatotoxicity.

1982 ◽  
Vol 101 (5) ◽  
pp. 782-785 ◽  
Author(s):  
Yoshinobu Ohtani ◽  
Fumio Endo ◽  
Ichiro Matsuda

PEDIATRICS ◽  
1994 ◽  
Vol 93 (6) ◽  
pp. 891-892
Author(s):  
Richard I. Kelley

Carnitine is a simple, vitamin-like compound that transports long-chain fatty acids into mitochondria. Despite its essential role in human nutrition and metabolism, carnitine engendered relatively little medical interest until the description in the 1970s of human disorders in which muscle or systemic levels of carnitine were markedly depressed and in which clinical improvement followed treatment with carnitine. Since then, carnitine has enjoyed a remarkable rise in popularity as an aid to everything from common muscle fatigue to treatment of specific inborn errors of metabolism. Nowhere has the popularity of carnitine been more evident than in the treatment of children taking valproic acid, which causes in some children a depression of free carnitine levels.


2007 ◽  
Vol 20 (1) ◽  
pp. 82-92 ◽  
Author(s):  
Carol A. Ott ◽  
Noll Campbell ◽  
Elayne A. Dworek

Valproic acid is used in psychiatry as a mood stabilizer and can be very effective in reducing symptoms of agitation. Valproic acid may cause hyperammonemia through carnitine deficiency created by its inhibition of mitochondrial enzymes in the urea cycle. Clinical presentation of hyperammonemia usually involves lethargy and somnolence, which may also be noted with therapeutic serum concentration during valproic acid therapy. The diagnosis of hyperammonemia is often overlooked due to a clinical presentation that may include normal liver enzyme tests and serum valproate levels that are within the therapeutic range. Treatment modalities may include discontinuation of valproic acid therapy, lactulose, naloxone, and hemodialysis. Carnitine supplementation, for both prevention and acute treatment of hyperammonemia, has been anecdotally reported and may be considered. This article illustrates a case of an adult male with schizoaffective disorder who was treated with valproic acid and subsequently developed hyperammonemia, despite therapeutic valproic acid serum levels and normal liver enzyme tests. Possible causes of hyperammonemia and current treatment options will be described, as well as suggestions for monitoring for this adverse event in the clinical setting.


2011 ◽  
Vol 12 (8) ◽  
pp. 1107-1117 ◽  
Author(s):  
Chin-Chuan Hung ◽  
Jia-Ling Ho ◽  
Wei-Lun Chang ◽  
John Jen Tai ◽  
Tsung-Jen Hsieh ◽  
...  

1987 ◽  
Vol 10 (1) ◽  
pp. 80-86 ◽  
Author(s):  
T. Lerman-Sagie ◽  
M. Statter ◽  
G. Szabo ◽  
P. Lerman

PEDIATRICS ◽  
1979 ◽  
Vol 64 (4) ◽  
pp. 521-521
Author(s):  
Paul B. Batalden ◽  
Bruce J. Van Dyne ◽  
James Cloyd

Since submission of this manuscript, two additional cases of pancreatitis associated with valproic acid therapy have been reported.18


JAMA ◽  
1980 ◽  
Vol 244 (8) ◽  
pp. 785-788 ◽  
Author(s):  
D. L. Coulter

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