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Published on: December 6, 2016
Abnormal interaction between cortical regions of obstructive sleep apnea hypopnea syndrome children
Naikai Shi1, Feng Pang2,3,4, Jin Chen1
1Key Laboratory of Brain, Cognition and Education Science, Ministry of Education, China; Institute for Brain Research and Rehabilitation, and Guangdong Key Laboratory of Mental Health and Cognitive Science, South China Normal University, 510631 Guangzhou, China.
Insights
Children with obstructive sleep apnea hypopnea syndrome show altered brain network activity. These changes in information flow patterns may serve as potential biomarkers for diagnosing the condition in pediatric patients.
Area of Science:
- Neuroscience
- Pediatric Sleep Medicine
- Biomarker Discovery
Background:
- Obstructive sleep apnea hypopnea syndrome (OSAHS) in children impairs cognitive function.
- Understanding the neural network alterations in pediatric OSAHS is crucial for early diagnosis and intervention.
Purpose of the Study:
- To identify potential electroencephalography (EEG) network biomarkers for pediatric obstructive sleep apnea hypopnea syndrome.
- To investigate differences in cortical information interaction and flow patterns between children with and without OSAHS.
Main Methods:
- Utilized symbolic transfer entropy to construct effective brain networks and assess cortical information interaction.
- Analyzed information flow patterns using cross-within variation and posterior-anterior information flow ratios.
- Compared EEG network parameters across sleep stages (N1, N2, N3, REM) in mild OSAHS, severe OSAHS, and healthy control groups.
Main Results:
- Pediatric OSAHS patients exhibited significantly higher symbolic transfer entropy in N1, N2, and REM stages (P<0.05) and lower in N3 stage (P<0.005) compared to controls.
- The β frequency band showed significantly lower cross-within variation across all sleep stages in the OSAHS group (P<0.05).
- Mild OSAHS children demonstrated significantly higher posterior-anterior information flow in the β frequency band during REM sleep (P<0.05).
Conclusions:
- Altered EEG network dynamics, specifically in information flow and transfer entropy, are characteristic of pediatric obstructive sleep apnea hypopnea syndrome.
- These distinct network patterns hold promise as potential biomarkers for diagnosing OSAHS in children.
- Findings offer novel insights into the neurophysiological mechanisms underlying cognitive deficits in pediatric OSAHS.
Abstract:
Obstructive sleep apnea hypopnea syndrome negatively affects the cognitive function of children. This study aims to find potential biomarkers for obstructive sleep apnea hypopnea syndrome in children by investigating the patterns of sleep electroencephalography networks. The participants included 16 mild obstructive sleep apnea hypopnea syndrome children, 12 severe obstructive sleep apnea hypopnea syndrome children, and 13 healthy controls. Effective brain networks were constructed using symbolic transfer entropy to assess cortical information interaction. The information flow pattern in the participants was evaluated using the parameters cross-within variation and the ratio of posterior-anterior information flow. Obstructive sleep apnea hypopnea syndrome children had a considerably higher symbolic transfer entropy in the full frequency band of N1, N2, and rapid eye movement (REM) stages (P < 0.05), and a significantly lower symbolic transfer entropy in full frequency band of N3 stage (P < 0.005), in comparison with the healthy controls. In addition, the cross-within variation of the β frequency band across all sleep stages were significantly lower in the obstructive sleep apnea hypopnea syndrome group than in the healthy controls (P < 0.05). What is more, the posterior-anterior information flowin the β frequency band of REM stage was significantly higher in mild obstructive sleep apnea hypopnea syndrome children than in the healthy controls (P < 0.05). These findings may serve as potential biomarkers for obstructive sleep apnea hypopnea syndrome in children and provide new insights into the pathophysiological mechanisms.
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