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Ketogenic diet improves sleep quality in children with therapy-resistant epilepsy
Tove Hallböök1, Johan Lundgren, Ingmar Rosén
1Division of Pediatrics, Department of Clinical Sciences, University Hospital, Lund, Sweden. tove.hallbook@skane.se
Insights
The ketogenic diet (KD) reduced total sleep time but improved sleep quality in children with drug-resistant epilepsy. Increased REM sleep correlated with better quality of life and reduced seizure severity.
Area of Science:
- Pediatric Neurology
- Sleep Medicine
- Epilepsy Management
Background:
- Therapy-resistant epilepsy in children presents significant challenges.
- The ketogenic diet (KD) is an established treatment for refractory epilepsy.
- Understanding KD's impact on sleep is crucial for comprehensive patient care.
Purpose of the Study:
- To investigate sleep structure changes in children with therapy-resistant epilepsy undergoing KD treatment.
- To correlate observed sleep alterations with clinical outcomes, including seizure control, quality of life, and behavior.
Main Methods:
- Ambulatory polysomnography was used to assess sleep in 18 children before and after 3 months of KD.
- Sleep parameters, seizure frequency/severity, quality of life, and behavior were evaluated.
- Eleven children continued KD and were reassessed at 12 months.
Main Results:
- KD significantly decreased total sleep and night sleep, but preserved slow-wave sleep.
- Rapid eye movement (REM) sleep increased, while stage 2 sleep decreased.
- Significant improvements were observed in seizure frequency, severity, quality of life, and attentional behavior, correlating with increased REM sleep and improved QOL.
Conclusions:
- The ketogenic diet alters sleep patterns in children with therapy-resistant epilepsy, notably decreasing total sleep but enhancing sleep quality.
- Increased REM sleep appears to be a key factor contributing to the observed improvements in quality of life and seizure control.
Purpose:
The study purpose was to evaluate sleep structure during ketogenic diet (KD) treatment in children with therapy-resistant epilepsy and to correlate possible alterations with changes in clinical effects on seizure reduction, seizure severity, quality of life (QOL), and behavior.
Methods:
Eighteen children were examined with ambulatory polysomnographic recordings initially and after 3 months of KD treatment. Eleven children continued with the KD and were also evaluated after 12 months. Sleep parameters were estimated. Seizure frequency was recorded in a diary and seizure severity in the National Health Seizure Severity Scale (NHS3). QOL was assessed with a visual analogue scale. Child behavior checklist and Ponsford and Kinsella's rating scale of attentional behavior were used.
Results:
KD induced a significant decrease in total sleep (p = 0.05) and total night sleep (p = 0.006). Slow wave sleep was preserved, rapid eye movement (REM) sleep increased (p = 0.01), sleep stage 2 decreased (p = 0.004), and sleep stage 1 was unchanged. Eleven children continued with the KD and were also evaluated after 12 months. They showed a significant decrease in daytime sleep (p = 0.01) and a further increase in REM sleep (p = 0.06). Seizure frequency (p = 0.001, p = 0.003), seizure severity (p < 0.001, p = 0.005) and QOL (p < 0.001, p = 0.005) were significantly improved at 3 and 12 months. Attentional behavior was also improved, significantly so at 3 months (p = 0.003). There was a significant correlation between increased REM sleep and improvement in QOL (Spearman r = 0.6, p = 0.01) at 3 months.
Conclusion:
KD decreases sleep and improves sleep quality in children with therapy-resistant epilepsy. The improvement in sleep quality, with increased REM sleep, seems to contribute to the improvement in QOL.
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