PT22 - MODIFIED KETOGENIC DIET THERAPY REDUCES SEIZURES AND PREVENTS LIVER STEATOSIS IN PATIENTS WITH REFRACTORY EPILEPSY

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PT22

MODIFIED KETOGENIC DIET THERAPY REDUCES SEIZURES AND PREVENTS LIVER STEATOSIS IN PATIENTS WITH REFRACTORY EPILEPSY

C. G. Marques1,*, J. G. de Souza1, N. R. T. Damasceno1,2

1Faculty of Medicine, 2Faculty of Public Health, University of São Paulo, São Paulo, Brazil

 

Rationale: Ketogenic diet (KD) is a well-established adjuvant treatment for pharmacoresistant epilepsy. We developed a Modified Ketogenic Diet (MKD) and evaluated its efficacy on epileptic seizure reduction and metabolic parameters control in patients with refractory epilepsy.

Methods: Clinical trial involved children of both sexes. MKD with <20% in saturated fatty acids, >50% increase in unsaturated fatty acids, and a 50% reduction in the ω6/ω3 ratio compared to classic KD. Following parameters were analyzed at baseline, 3- and 6 months: seizure frequency, lipid profile, glucose, liver biomarkers (AST, ALT, GGT, ALP), using ELISA kits; and liver ultrasound. RM-ANOVA or the Friedman test, with the Bonferroni post-test, was used.

Results: Fifteen patients (4.5±2.6y, 80% male, 40% had structural/metabolic etiology epilepsy, 40% had unknown etiology epilepsy, and 20% had genetic etiology epilepsy). At T0, patients had a median of 9 seizures/day (min.=0–max.=60), at T1 there was a reduction to 2 seizures (min.=0– max.=15), and at T2 to 1 daily seizure (min.=0– max.=20) (p<0.01). Thus, MKD promoted a 66.7% reduction in seizures throughout the follow-up. As an adverse effect, triglycerides increase (T0=70.4±33.5mg/dL, T2 =110.0±57.0mg/dL, p=0.03). A decrease in ALP was noted (T0=199.8±64.5U/L, T2=133.3± 38.6U/L, p=0,01), without clinically relevant changes in the other liver enzymes. As expected, there was a decrease in blood glucose levels (T0=82.8±14.6mg/dL;T2=72.9±9.9mg/dL, p=0.02). Ultrasonography revealed the presence of a regular liver surface, homogenous liver echotexture, usual echogenicity, absence of attenuation, and absence of liver steatosis in all patients throughout the intervention.

Conclusion: Six months of MKD was effective in reducing seizures in children with refractory epilepsy, but induced hypertriglyceridemia without significant changes in the incidence of liver steatosis. 

Disclosure of Interest: None declared