Modified Atkins diet versus topiramate in young children with epileptic spasms refractory to steroids and vigabatrin:

Rashmi Meena1, Sayoni Roy Chowdhury1, Aman Elwadhi2

  • 1Department of Paediatrics, Lady Hardinge Medical College and Associated Kalawati Saran Children's Hospital, New Delhi, India.

Seizure
|August 21, 2025
PubMed

Insights

The Modified Atkins Diet (MAD) is more effective than Topiramate for treating infantile epileptic spasms refractory to initial therapies. This dietary intervention showed significant improvements in spasm reduction and alertness.

Area of Science:

  • Pediatric Neurology
  • Epileptology
  • Clinical Nutrition

Background:

  • Limited evidence exists for treating infantile epileptic spasm syndrome (IESS) after first-line treatments fail.
  • Hormonal therapy and vigabatrin are common first-line treatments for IESS.

Purpose of the Study:

  • To compare the efficacy and tolerability of the Modified Atkins Diet (MAD) against Topiramate in children with IESS who did not respond to initial therapies.
  • To evaluate spasm frequency, electroencephalographic (EEG) improvements, and non-seizure domain changes.

Main Methods:

  • A randomized open-label trial involving 80 children with IESS.
  • Participants were randomized to either the Modified Atkins Diet (MAD) or Topiramate.
  • Assessments at 12 weeks included spasm frequency, BASED score for EEG, adverse effects, and non-seizure improvements.

Main Results:

  • The MAD group showed statistically significant improvements in >50% spasm reduction (67.5% vs. 42.5%) and >90% spasm reduction (22.5% vs. 4.76%) compared to Topiramate.
  • MAD also led to greater improvement in the BASED score (40% vs. 12.5%) and alertness (17.5% vs. 2.5%).
  • Both treatments were generally well-tolerated with mild side effects.

Conclusions:

  • The Modified Atkins Diet (MAD) is a more effective treatment option than Topiramate for refractory infantile epileptic spasms.
  • Further research with larger cohorts and extended follow-up is needed to validate these findings.
  • ClinicalTrials.gov identifier: NCT05958160.
Abstract

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