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Published on: December 22, 2016
Sleep Apnea Specific Hypoxic Burden in Children With Down Syndrome and Typically Developing Children
Lisa M Walter1, Dhruv Bhatnagar1, Miles B H Ong1
1Department of Paediatrics, Monash University, Melbourne, Australia.
Insights
Hypoxic burden (HB) impacts children with obstructive sleep apnea (OSA). Higher HB in children with Down syndrome (DS) correlates with dampened autonomic function, highlighting the need for OSA treatment in this population.
Area of Science:
- Pediatric Sleep Medicine
- Cardiology
- Genetics
Background:
- Hypoxic burden (HB) quantifies respiratory event-related desaturations and is linked to cardiovascular disease in adults with obstructive sleep apnea (OSA).
- HB has not been evaluated in typically developing (TD) children with OSA or in children with Down syndrome (DS), who exhibit a higher prevalence and severity of OSA-related hypoxia.
- Children with DS face increased risks for OSA and associated cardiovascular complications.
Purpose of the Study:
- To investigate the relationship between hypoxic burden (HB) and heart rate variability (HRV) in children with Down syndrome (DS) and typically developing (TD) children with OSA.
- To compare HB levels between children with DS and TD children across different OSA severity groups.
- To determine if HB predicts HRV, an indicator of cardiovascular health, in these pediatric populations.
Main Methods:
- Overnight polysomnography was conducted on 44 children (3-19 years) with DS and matched TD children.
- Participants were categorized into primary snoring (PS), Mild OSA, or Moderate/Severe (MS) OSA groups.
- Heart rate variability (HRV) was analyzed using power spectral analysis, and regression analysis assessed the predictive value of HB on HRV.
Main Results:
- Children with MS OSA in both groups exhibited significantly higher HB than those with PS or Mild OSA.
- Children with DS and PS or Mild OSA had elevated HB compared to their TD counterparts, with no significant difference in the MS OSA groups.
- Hypoxic burden (HB) was found to predict dampened sympathetic and parasympathetic activity specifically in children with DS (R² = 0.12, p = 0.03).
Conclusions:
- Children with DS and PS or Mild OSA demonstrate higher hypoxic burden (HB) than TD children.
- Elevated HB in children with DS is associated with reduced autonomic function, suggesting potential cardiovascular implications.
- These findings underscore the critical importance of identifying and treating obstructive sleep apnea (OSA) in children with Down syndrome (DS) to mitigate adverse effects on autonomic function.
Abstract:
Hypoxic burden (HB) is a measure incorporating frequency, depth and duration of respiratory event-related desaturations. While HB is associated with cardiovascular disease in adults with obstructive sleep apnea (OSA), it has not been assessed in typically developing (TD) children with OSA, nor in children with Down syndrome (DS), who have a higher incidence of OSA with more severe hypoxia. We assessed whether HB in these children was related to heart rate variability (HRV), an indicator of cardiovascular outcomes. Children (3-19 years, n = 44) with DS and TD children matched for OSA severity, age and sex underwent overnight polysomnography and were grouped into primary snoring (PS), Mild or Moderate/Severe (MS) OSA. HRV was analysed using power spectral analysis of the electrocardiograph. Regression analysis determined whether HB was predictive of HRV. Children with MS OSA in both groups had higher HB compared with children with PS (p < 0.001 for both) and Mild OSA (DS, p < 0.001; TD, p < 0.05). Children with DS and PS or Mild OSA had higher HB compared with TD children (PS p < 0.05; Mild OSA p < 0.001). There was no difference between the MS OSA groups. HB predicted dampened sympathetic and parasympathetic activity only in children with DS (R 2 = 0.12, β = -10.6, SE = 4.6, p = 0.03). HB was higher in children with DS and PS or Mild OSA compared to TD children and predicted dampened autonomic function in children with DS. The potential contribution of the adverse effects of HB on autonomic function adds weight to the importance of identifying and treating OSA in children with DS.
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