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IMPAIRED FATTY-ACID OXIDATION IN CHILDREN ON VALPROIC ACID AND THE EFFECT OF L-CARNITINE
被引:32
作者:
KOSSAK, BD
SCHMIDTSOMMERFELD, E
SCHOELLER, DA
RINALDO, P
PENN, D
TONSGARD, JH
机构:
[1] UNIV CHICAGO,DEPT NEUROL,CHICAGO,IL 60637
[2] UNIV CHICAGO,DEPT PEDIAT,CHICAGO,IL 60637
[3] UNIV CHICAGO,DEPT MED,CHICAGO,IL 60637
[4] UNIV CHICAGO,JOSEPH KENNEDY MENT RETARDAT CTR,CHICAGO,IL 60637
[5] YALE UNIV,DEPT GENET,NEW HAVEN,CT 06520
来源:
关键词:
D O I:
10.1212/WNL.43.11.2362
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Fatty acid oxidation was studied in 12 patients (aged 3 to 19 years) receiving valproic acid (VPA), predominantly as monotherapy, before and after 1 month of L-carnitine supplementation (50 mg/kg/day po) in order to determine whether L-carnitine plays a role in preventing the hepatotoxic effects of this drug. Five of these patients were also studied prior to VPA treatment. Only one patient taking VPA had an abnormally low plasma free carnitine. Acyl-/free carnitine ratios were elevated in five patients on VPA and normalized after L-carnitine supplementation. Mean plasma concentrations of free fatty acids, beta-OH-butyrate, and cumulative excretion of (CO2)-C-13 after administration of 1-C-13-octanoic acid were not changed by VPA or L-carnitine treatment. Urinary dicarboxylic acids, acylglycines, and octanoylcarnitine were elevated during VPA therapy and unaltered by L-carnitine. These results suggest that, in patients at low risk for VPA-induced hepatotoxicity (patients aged >2 years and taking VPA as monotherapy), VPA causes metabolic abnormalities resembling those found in inborn errors of mitochondrial beta-oxidation which are not corrected by L-carnitine.
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页码:2362 / 2368
页数:7
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