The ketogenic diet: Uses in epilepsy and other neurologic illnesses
Open accessAbstract
The ketogenic diet is well established as therapy for intractable epilepsy. It should be considered first-line therapy in glucose transporter type 1 and pyruvate dehydrogenase deficiency. It should be considered early in the treatment of Dravet syndrome and myoclonic-astatic epilepsy (Doose syndrome). Initial studies indicate that the ketogenic diet appears effective in other metabolic conditions, including phosphofructokinase deficiency and glycogenosis type V (McArdle disease). It appears to function in these disorders by providing an alternative fuel source. A growing body of literature suggests the ketogenic diet may be beneficial in certain neurodegenerative diseases, including Alzheimer disease, Parkinson's disease, and amyotrophic lateral sclerosis. In these disorders, the ketogenic diet appears to be neuroprotective, promoting enhanced mitochondrial function and rescuing adenosine triphosphate production. Dietary therapy is a promising intervention for cancer, given that it may target the relative inefficiency of tumors in using ketone bodies as an alternative fuel source. The ketogenic diet also may have a role in improving outcomes in trauma and hypoxic injuries.
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The ketogenic diet is a high-fat, low-carbohydrate diet that mimics the metabolic effects of starvation by forcing the body to use its primary fat reserves.
“The ketogenic diet is a high-fat, low-carbohydrate diet that mimics the metabolic effects of starvation by forcing the body to use its primary fat reserves (Barañano, 2008).”
From The Microbiota-Gut-Brain Axis (2019) · cites this paper as Barañano, 2008
The Introduction describes the ketogenic diet as very high in fat and low in carbohydrates and says it is thought to simulate starvation by making the body use primarily fat for fuel. It says the body metabolizes fat stores during fasting, but does not say the diet forces use of the body's fat reserves rather than dietary fat. (LLM, conf=0.84)
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- Authors
- Barañano, K. W., & Hartman, A. L.
- Affiliations
- Johns Hopkins University (US)
- Corresponding author
- Hartman, Adam L.
- ORCID
- Hartman, Adam L.
- Venue
- Current Treatment Options in Neurology
- Published
- 2008-11
- Volume
- 10
- Issue
- 6
- Pages
- 410-419
- ISSN
- 1092-8480 (ISSN-L)
- 1534-3138
- PMC
- PMC2898565
- OpenAlex
- W2023983971
- Cited by
- 239
- References
- 6
- Citations by year
- 2026: 1 · 2025: 9 · 2024: 12 · 2023: 11 · 2022: 16 · 2021: 17 · 2020: 26 · 2019: 24 · 2018: 21 · 2017: 15 · 2016: 20 · 2015: 11 · 2014: 14 · 2013: 11 · 2012: 10
- FWCI
- 4.53
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Current Treatment Options in Neurology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (K12NS001696)
- Topics
- Health Sciences › Medicine › Physiology › Diet and metabolism studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
- Health Sciences › Medicine › Psychiatry and Mental health › Epilepsy research and treatment
- Keywords
- ketogenic diet, drug-resistant epilepsy, pyruvate dehydrogenase deficiency, Dravet syndrome, myoclonic-astatic epilepsy, phosphofructokinase deficiency, McArdle disease, neurodegenerative diseases, Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, neuroprotection, mitochondrial function, ATP production, cancer therapy, ketone bodies, hypoxic injury, trauma (physical injury)
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