Abstract
The ketogenic diet (KD) is a treatment of infantile spasms (IS). Here, we examine the efficacy of KD in medically refractory IS, examine its impact on growth in infants, and explore its mechanism of action. At 1-3 months after the initiation of the KD, 46% of twenty-six patients had a greater than 90% reduction in IS. No significant relationships between reduction in IS and serum β-hydroxybutyrate, or glucose levels were identified. Also, the KD had not significantly altered patient's growth parameters. Thus, in corroborating with prior studies, we demonstrate the KD is a well-tolerated and efficacious treatment of IS.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 172-175 |
| Number of pages | 4 |
| Journal | Epilepsy Research |
| Volume | 96 |
| Issue number | 1-2 |
| DOIs | |
| State | Published - Sep 2011 |
| Externally published | Yes |
Keywords
- Anthropometry
- Ketogenic diet
- Ketone bodies
- Refractory epilepsy
- West syndrome
ASJC Scopus subject areas
- Neurology
- Clinical Neurology
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