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Sleep disorders in pediatric patients with agenesis of the corpus callosum
Ashley Kwon1, Payal Kenia Gu1,2,3, Christina Zhang1,2
1Keck School of Medicine of the University of Southern California, Los Angeles, California.
Insights
Children with agenesis of the corpus callosum (ACC) often experience poor sleep quality and obstructive sleep apnea (OSA). Early screening for sleep disorders is recommended for these pediatric patients.
Area of Science:
- Pediatric Neurology
- Sleep Medicine
- Neurodevelopmental Disorders
Background:
- Agenesis of the corpus callosum (ACC) is a congenital brain malformation with limited research on associated sleep disturbances.
- Understanding sleep architecture and respiratory patterns in children with ACC is crucial for comprehensive care.
Purpose of the Study:
- To characterize sleep architecture and respiratory parameters in pediatric patients diagnosed with agenesis of the corpus callosum.
- To identify common sleep-related issues and their prevalence in this population.
Main Methods:
- Retrospective analysis of polysomnography data from 20 pediatric patients with ACC (2000-2023).
- Evaluation of demographic data, associated conditions, and sleep quality indicators (National Sleep Foundation criteria, arousal index).
- Statistical comparison between complete and partial ACC groups using Fisher's exact test or unpaired t-test.
Main Results:
- 15/20 patients exhibited poor sleep quality, with decreased sleep efficiency and rapid eye movement (REM) sleep being common.
- 9/20 patients had an increased arousal index, indicating fragmented sleep.
- 11/18 patients were diagnosed with obstructive sleep apnea (OSA), which was more prevalent in children under 3 years old.
Conclusions:
- Pediatric patients with ACC frequently present with poor sleep quality and a high incidence of obstructive sleep apnea.
- No significant differences in sleep quality or OSA prevalence were observed between complete and partial ACC.
- The findings underscore the importance of routine screening for sleep disorders in children with agenesis of the corpus callosum.
Study Objectives:
There is limited information about sleep in agenesis of the corpus callosum (ACC). We aim to describe the sleep architecture and respiratory parameters of children with ACC.
Methods:
We performed a retrospective study of 20 patients with ACC who had polysomnography between 2000 and 2023. Demographic data, body mass index or weight for length, associated conditions, and polysomnography findings were collected. National Sleep Foundation sleep quality indicators as well as increased polysomnography arousal index ≥ 10 events/h were used in the analysis. Fisher's exact test or unpaired t test was used to compare groups.
Results:
Average age was 5.9 ± 5.4 years old. A total of 12/20 patients were male; 6/20 were overweight/obese; 14/20 had complete ACC, and 6/20 had partial ACC; 8/20 had seizures; 15/20 had ≥ 1 National Sleep Foundation poor sleep quality indicator (decreased sleep efficiency [45%], decreased rapid eye movement sleep [53%]); and 9/20 had increased arousals. Between complete and partial ACC, there was no difference in presence of ≥ 1 poor sleep quality indicator (P = .61), sleep efficiency (P = .34), rapid eye movement sleep (P = .28), and arousals (P = 1.0). 11/18 had obstructive sleep apnea (OSA); 5/11 had associated central sleep apnea. There was no difference in OSA between those with complete and partial ACC (P = 1.0). OSA was associated with children < 3 years old (P = .01).
Conclusions:
Children with ACC have poor sleep quality, and many have OSA. There was no difference in sleep quality or presence of OSA between those with complete and partial ACC. OSA was seen more in younger children. Our study supports the need for screening of sleep-related disorders in patients with ACC.
Citation:
Kwon A, Gu PK, Zhang C, Davidson Ward SL, Perez IA. Sleep disorders in pediatric patients with agenesis of the corpus callosum. J Clin Sleep Med. 2024;20(10):1663-1667.
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