KETONEMIA AND SEIZURES - METABOLIC AND ANTICONVULSANT EFFECTS OF 2 KETOGENIC DIETS IN CHILDHOOD EPILEPSY
KETONEMIA AND SEIZURES - METABOLIC AND ANTICONVULSANT EFFECTS OF 2 KETOGENIC DIETS IN CHILDHOOD EPILEPSY
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DOI:
10.1203/00006450-197605000-00006
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发表时间:
1976-01-01
影响因子:
3.6
通讯作者:
HUTTENLOCHER, PR
中科院分区:
文献类型:
--
作者:
HUTTENLOCHER, PR
Metabolic effects of a new ketogenic regimen in which ketonemia is induced by feeding of medium chain triglycerides (MCT) are described, and comparisons are made with effects of the standard high fat ketogenic diet. Eighteen children maintained on the MCT diet for 3 mo. to 4 yr failed to show elevations of serum cholesterol and had only a slight rise in serum total fatty acids, in contrast to the marked hyperlipidemia observed in children on the standard high fat diet. Long term use of the MCT diet did not affect pH of venous blood. Blood glucose fell below 50 mg/100 ml in 1/3 of the children, the lowest levels being reached 2-3 wk after the start of the diet. Plasma D(-)-.beta.-hydroxybutyrate (BHB) and acetoacetate rose gradually after institution of diet therapy, maximum levels being reached after about 1 mo. Higher levels of BHB and acetoacetate were achieved in children under the age of 10 yr (BHB = 4.3 mM .+-. 0.6 SEM, acetoacetate = 1.8 mM .+-. 0.3 SEM) than in 10-18 yr olds (BHB = 1.6 mM .+-. 0.2 SEM, acetoacetate = 0.57 mM .+-. 0.08 SEM). Plasma BHB and acetoacetate levels in children maintained on a 3:1 high fat diet were similar to those in children on a 60% MCT diet. Plasma levels of BHB showed a significant correlation with anticonvulsant effect (P < 0.02). Both the ketonemia and the anticonvulsant action were reversed rapidly by i.v. infusion of glucose. The anticonvulsant effect of the standard ketogenic diet and of the MCT diet are dependent upon maintenance of blood levels of BHB above 2 mM and of acetoacetate above 0.6 mM. One or both of these compounds either have direct anticonvulsant effects or produce rapidly reversible changes in cerebral metabolism, which in turn affect cerebral excitability.