Effect of the classic ketogenic diet on the treatment of refractory epileptic seizures

Authors

  • Luciana Duarte MARTINS Universidade de São Paulo
  • Vera Cristina TERRA Universidade de São Paulo
  • Carolina Ferreira NICOLETTI Universidade de São Paulo
  • Paula Garcia CHIARELLO Universidade de São Paulo
  • Julio Sérgio MARCHINI Universidade de São Paulo
  • Américo Ceiki SAKAMOTO Universidade de São Paulo
  • Carla Barbosa NONINO-BORGES Universidade de São Paulo

Keywords:

Epilepsy, Ketogenic diet, Nutritional status

Abstract

Objective
The ketogenic diet is used as a therapeutic alternative for the treatment of epilepsy in patients with refractory epilepsy. It simulates biochemical changes typical of fasting. The present study verified the nutritional impact of the ketogenic diet on children with refractory epilepsy.

Methods
Nutritional status data (dietary, biochemical and anthropometric measurements), seizure frequency, and adverse events were collected from the medical records and during outpatient clinic visits of children over a period of 36 months.

Results
Of the 29 children who initiated the ketogenic diet, 75.8% presented fewer seizures after one month of treatment. After six months, 48.3% of the patients had at least a 90.0% decrease in seizure frequency, and 50.0% of these patients presented total seizure remission. At 12 months, eight patients continued to show positive results, and seven of these children remained on the ketogenic diet for 24 months. There was an improvement of the nutritional status at 24 months, especially in terms of weight, which culminated with the recovery of proper weight-for-height. There were no significant changes in biochemical indices (total cholesterol and components, triglycerides, albumin, total protein, creatinine, glycemia, serum aspartate transaminase and
serum alanine transaminase). Serum cholesterol levels increased significantly in the first month, fell in the following six months, and remained within the normal limits thereafter.

Conclusion
In conclusion, patients on the classic ketogenic diet for at least 24 months gained weight. Moreover, approximately one third of the patients achieved significant reduction in seizure frequency, and some patients achieved total remission. 

References

Kossoff EH, Zupec-Kania BA, Rho JM. Ketogenic diets: an update for child neurologists. J Child Neurol. 2009; 24(8):979-88.

Kessler SK, Neal EG, Camfield CS, Kossoff EH. Dietary therapies for epilepsy: future research. Epilep Behav. 2011; 22(1):17-22.

Kossoff EH, Zupec-Kania BA, Amark PE, et al. Optimal clinical management of children receiving the ketogenic diet: recommendations of the International Ketogenic Diet Study Group. Epilepsia. 2009; 50(2):304-17.

Bainbridge JL, Gidal BE, Ryan M. The ketogenic diet. Pharmacoterapy. 1999; 19(6):782-6.

Kelley SA, Kossoff EH. Doose syndrome (myoclonicastatic epilepsy): 40 years of progress. Dev Med Child Neurol. 2010; 52:988-93.

Schwartz RH, Eaton J, Bower BD. Ketogenic diets in the treatment of epilepsy: short-term clinical effects. Dev Med Child Neurol. 1989; 31(2):145-51.

The American Dietetic Association. Manual of clinical dietetics. Chicago: The American Dietetic Association; 1998. p.455-66.

Freeman JM, Vining EPG, Pillas DJ, Pyzik PL, Casey JC, Kelly LM. The efficacy of ketogenic diet: a prospective evolution of intervention in 150 children. Pediatrics. 1998; 102(6):1358-63.

Neal EG, Cross JH. Efficacy of dietary treatments for epilepsy. J Hum Nutr Diet. 2010; 23:113-9.

Huffman J, Kossoff HE. State of the ketogenic diet(s) in epilepsy. Epilepsia. 2007; 48:43-58.

Katyal NG, Koehler AN, McGhee B, Foley CM, Crumrine PK. Ketogenic diet in refractory epilepsy: the experience of children’s Hospital of Pittsburgh. Clin Pediatr. 2000; 39(3):153-9.

Artigas J. Psychological manifestations of epilepsy in childhood. Rev Neurol. 1999; 28(Suppl 2): S135-41.

Volpe SL, Schall JI, Gallagher PR, Stallings VA, Bergqvist AGC. Nutrient intake of children with intractable epilepsy compared with healthy children. J Am Diet Assoc. 2007; 107(6):1014-18.

Richard D, Ferland J, Lalonde J, Samson P, Deshaies Y. Influence of topiramate in the regulation of energy balance. Nutrition. 2000; 16(10):961-6.

Thommessen M, Kase BF, Riis G, Heiberg A. The impact of feeding problems on growth and energy intake in children with cerebral palsy. Eur J Clin Nutr. 1991; 45(10):479-87.

Bertoli S, Cardinali P, Veggiotti P, Trentani C, Testolin G, Tagliabue A. Evaluation of nutritional status in children with refractory epilepsy. Nutr J. 2006; 5: 14-22.

Mainardi P, Albano C. Is the antiepileptic effect of the ketogenic diet due to ketones? Med Hypotheses. 2008; 70(3):536-9.

Wheless JW. Nonpharmacologic treatment of the catastrophic epilepsies of childhood. Epilepsia. 2004; 45(Suppl 5):S17-22.

Hauser W, Hesdorffer DC. The natural history of seizures. In: Wyllie E. The treatment of epilepsy: principles and practice. Baltimore: Williams & Wilkins; 1996. p.173-8.

Commission on Classification and Terminology of the International League Against Epilepsy. Proposal for revised classification of epilepsies and epileptic syndromes. Epilepsia. 1989; 30(4):389-99.

Waterlow JC. Note on the assessment and classification of protein-energy malnutrition in children. Lancet. 1973; 14(2):87-9.

National Center for Health Statistics. NCHS Growth curves for children birth - 18 years. Washington (DC): Government Printing Office; 1977. Departament of Health Education and Welfare publication nº (PHS) 78-1650. Vital and Health Statistics; serie 11; n.165.

Papandreou D, Pavlou E, Kalimeri E, Mavromichlis I. The ketogenic diet in children with epilepsy. Br J Nutr. 2006; 95(1):5-13.

Liu YMC, Williams S, Basualdo-Hommond C, Stephens D, Curtis R. A prospective study: growth and nutrition status of children treated with the ketogenic diet. J Am Diet Assoc. 2003; 103(6): 707-12.

Williams S, Basualdo-Hammond C, Curtis R. Growth retardation in children with epilepsy on the ketogenic diet: a retrospective chart review. J Am Diet Assoc. 2002; 102(3): 405-7.

Tumas R, Lopes Cardoso A, Marques-Dias MJ, Vieira MA. Ketogenic diet in epileptic children: clinical and laboratory assessment. Nutr Hosp. 2010; 25(2): 317-8.

Peterson SJ, Tangney CC, Pimentel-Zablah EM, Hjelmgren B, Booth G, Berry-Kravis E. Changes in growth and seizure reduction in children on the ketogenic diet as a treatment for intractable epilepsy. J Am Diet Assoc. 2005; 105(5):718-25.

Freeman JM, Kossof EH, Hartman AL. The ketogenic diet: one decade later. Pediatrics. 2007; 119: 535-43.

Hosain SA, Vega-Talbott ML, Solomon GE. Ketogenic diet in pediatric epilepsy patients with gastrostomy feeding. Pediatr Neurol. 2004; 32(2): 81-3.

Kim DW, Kang HC, Park JC, Kim HD. Benefits of the nonfasting ketogenic diet compared with the initial fasting ketogenic diet. Pediatrics. 2004; 114(6):1627-30.

Kang HC, Kim YJ, Kim DW, KimHD. Efficacy and Safety of the ketogenic diet for intratable epilepsy: korean multicentric experience. Epilepsia. 2005; 46(2):272-9.

Hartman AL, Vining EPG. Clinical aspects of the ketogenic diet. Epilepsia. 2007; 48(1):31-42.

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Published

2023-08-24

How to Cite

Duarte MARTINS, L. ., TERRA, V. C., Ferreira NICOLETTI, C. ., Garcia CHIARELLO, P. ., MARCHINI, J. S., Ceiki SAKAMOTO, A., & Barbosa NONINO-BORGES, C. . (2023). Effect of the classic ketogenic diet on the treatment of refractory epileptic seizures. Brazilian Journal of Nutrition, 25(5). Retrieved from https://periodicos.puc-campinas.edu.br/nutricao/article/view/9288

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ORIGINAL ARTICLE