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LGS Treatments
Diet
Types of Dietary Therapy
Dietary therapies can help control various types of seizures in both children and adults when medicines alone don’t work. There are four major dietary therapies used today for epilepsy. They are all low in carbohydrates (like sugar, pasta, and bread) and high in fat (like butter, oils, bacon, and avocados).
Types of Diets to Treat Seizures
- Ketogenic Diet (KD)
- Medium-Chain Triglyceride (MCT) Diet
- Modified Atkins Diet (MAD)
- Low Glycemic Index Diet (LGID)
Ketogenic Diet
The Keto Diet is very high in fat and very low in protein and carbohydrates. It is designed to make the body burn fat instead of carbohydrates as the main source of energy. The body will go into ketosis as a sign that fat is being burned, and this can be detected in the urine of those on the diet. This diet is often restricted to a small number of calories each day and strict amounts of fat, proteins, and carbohydrates.
Medium Chain Triglyceride (MCT) Diet
The MCT Diet is often used to supplement the Keto Diet by adding a specific type of fat called MCT. MCTs are smaller than most fats and easier to digest. They get absorbed into the blood quickly and turn the oil into usable energy. This diet adds MCT oil to supplement the fats consumed during the Keto Diet.
Modified Atkins Diet (MAD)
This diet, like the Keto Diet, is very high in fat and very low in protein and carbohydrates. It is less restrictive than the Keto Diet and allows for more calories and a wider variety of foods. With the MAD, foods are not weighed and measured as in the Keto Diet, and the amounts of fats, proteins, and carbohydrates are less restricted.
Low Glycemic Index Diet (LGID)
The LGID is an alternative to the Keto Diet and limits the type of carbohydrates a person can eat. This diet focuses on eating carbohydrates with a Low Glycemic Index, a measurement of how a food raises blood sugar. Low Glycemic Index foods (e.g., whole grain breads and berries) do not raise blood sugar as dramatically as those with a High Glycemic Index (e.g., candy and chips).
Comparison of Diet Therapies for Epilepsy
Swipe sideways to compare all four diets. Questions stay visible as you scroll.
| Questions | Classic and Modified Keto | MCT Oil | Low Glycemic Index Treatment | Modified Atkins |
|---|---|---|---|---|
| Is medical supervision required? | Yes | Yes | Yes | Yes |
| Is diet high in fat? | Yes | Yes | Yes | Yes |
| Is diet low in carbohydrate? | Yes | Yes | Yes | Yes |
| What is the ratio of fat to carbohydrate & protein? | 4:1, 3:1, 2:1, 1:1 | Approximately 1:1 | Approximately 1:1 | Approximately 2:1 |
| How much carbohydrate is allowed on a 1000 calorie diet? | 8gm carb on a 4:1; 16gm carb on a 3:1; 30gm carb on a 2:1; 40–60gm carb on a 1:1 | 40–50gm | 40–60gm | 10gm adolescents or 15gm adults for 1 month; 20gm afterwards |
| How are foods measured? | Weighed | Weighed or measured | Measured or estimated | Estimated |
| Are meal plans used? | Yes | Yes | Yes | Optional |
| Where is the diet started? | Hospital or Home | Hospital or Home | Home | Home |
| Are calories controlled? | Yes | Yes | Yes | No |
| Are vitamin and mineral supplements required? | Yes | Yes | Yes | Yes |
| Are liquids (fluids) restricted? | No | No | No | No |
| Is a pre-diet laboratory evaluation required? | Yes | Yes | Yes | Yes |
| Can there be side effects? | Yes | Yes | Yes | Yes |
| What is the overall difference in design of these diets? | Foods are weighed in grams; the ratio can be adjusted for stronger ketosis or for better tolerance. | Medium Chain Triglycerides (MCT) are highly ketogenic which allows more carbohydrate. | Low glycemic carbs in combination with fat results in steady glucose levels. | Loosely structured; fat is encouraged, protein is not limited but too much is discouraged. |
Statistics on Treatments for Epilepsy
Epilepsy is a diagnosis that is made after someone has had a seizure along with specific symptoms. An anti-seizure drug is typically tried as a first line of treatment. Some people are candidates for epilepsy surgery if their epilepsy is found to stem from a localized area of the brain.
Statistics on the success of anti-seizure drug treatment haven’t changed in 60 years.¹
- After trying the 1st drug, 47% become seizure-free; 53% continue having seizures.
- After trying the 2nd drug, 13% become seizure-free; 40% continue having seizures.
- After trying the 3rd drug, 1% become seizure-free; 39% continue having seizures.
This treatment failure is known as “medication resistant epilepsy”.
When Should Ketogenic Diet Therapy Be Considered?²
After trying a 2nd drug according to the International Ketogenic Diet Study Group’s published guidelines in 2018 and, sooner for some conditions (see chart below).
According to the 2016 Cochrane Review of evidence from 11 randomized controlled trials:³
Seizure freedom reached as high as 55% with the ketogenic diet and 10 to 25% with the Modified Atkins Diet (MAD). The proportion of individuals who had 50% or greater seizure reduction was as high as 85% in the ketogenic diet and 60% in MAD.
Ketogenic Diet Therapy Should Be Tried Earlier in the Course of Treatment for These Conditions²
Conditions where diet therapy should be considered:
- Angelman syndrome
- Complex 1 mitochondrial disorders
- Dravet syndrome³
- Epilepsy with myoclonic–atonic seizures (Doose syndrome)
- Glucose transporter protein 1 deficiency syndrome
- Febrile infection–related epilepsy syndrome
- Formula-fed (solely) children or infants
- Infantile spasms
- Ohtahara syndrome
- Pyruvate dehydrogenase deficiency
- Super-refractory status epilepticus
- Tuberous sclerosis complex
Conditions where diet therapy could be considered:
- Adenylosuccinate lyase deficiency
- CDKL5 encephalopathy
- Childhood absence epilepsy
- Cortical malformations
- Epilepsy of infancy with migrating focal seizures
- Epileptic encephalopathy with continuous spike-and-wave during sleep
- Glycogenosis type V
- Juvenile myoclonic epilepsy
- Lafora body disease
- Landau-Kleffner syndrome
- Lennox-Gastaut syndrome
- Phosphofructokinase deficiency
- Rett syndrome
- Subacute sclerosing panencephalitis
