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Updated: Nov 29, 2025

Measuring Cardiac Autonomic Nervous System ANS Activity in Children
Published on: April 29, 2013
Children with Down syndrome and sleep disordered breathing have altered cardiovascular control
Rosemary S C Horne1, Ashwini Sakthiakumaran2, Ahmad Bassam2
1The Ritchie Centre, Department of Paediatrics, Monash University and Hudson Institute of Medical Research, Melbourne, VIC, Australia. rosemary.horne@monash.edu.
Insights
Children with Down syndrome (DS) experience worse cardiovascular effects from sleep disordered breathing (SDB) than typically developing children. SDB in DS exacerbates autonomic dysfunction and hypoxia, increasing cardiovascular risks.
Area of Science:
- Cardiology
- Pediatrics
- Sleep Medicine
Background:
- Sleep disordered breathing (SDB) is linked to cardiovascular issues in typically developing (TD) children.
- Children with Down syndrome (DS) have a higher prevalence of SDB.
- The cardiovascular impact of SDB in children with DS is not well-understood.
Purpose of the Study:
- To compare the cardiovascular effects of SDB in children with DS to TD children with and without SDB.
- To investigate autonomic nervous system function and hypoxia exposure in relation to SDB severity across groups.
Main Methods:
- Matched cohort study comparing 44 children with DS to 44 TD children without SDB (TD-) and 44 TD children with SDB (TD+).
- ECG recordings analyzed for power spectral density (LF, HF, total power, LF/HF ratio) during sleep and wakefulness.
- Assessment of oxygen saturation (SpO2) parameters including nadir, average drop, and frequency of >4% drops.
Main Results:
- Children with DS exhibited reduced high-frequency (HF) power and increased LF/HF ratio, indicating impaired parasympathetic activity and sympathovagal imbalance.
- No significant differences in low-frequency (LF) power were observed between groups.
- The DS group showed significantly greater SpO2 nadir, average SpO2 drop, and frequency of SpO2 drops >4% compared to the TD+ group.
Conclusions:
- SDB significantly exacerbates autonomic dysfunction and hypoxia in children with DS compared to TD children.
- These findings suggest a heightened cardiovascular risk in children with DS experiencing SDB.
- Early screening and treatment of SDB in children with DS are recommended to mitigate adverse cardiovascular outcomes.
Background:
Sleep disordered breathing (SDB) in typically developing (TD) children is associated with adverse cardiovascular effects. As children with Down syndrome (DS) are at increased risk for SDB, we aimed to compare the cardiovascular effects of SDB in children with DS to those of TD children with and without SDB.
Methods:
Forty-four children with DS (3-19 years) were age and sex matched with 44 TD children without SDB (TD-) and with 44 TD children with matched severity of SDB (TD+). Power spectral density was calculated from ECG recordings, for low frequency (LF), high frequency (HF), total power and the LF/HF ratio.
Results:
Children with DS had lower HF power, and higher LF/HF during sleep and when awake. There were no differences between groups for LF power. SpO2 nadir, average SpO2 drop and SpO2 > 4% drop were larger in the DS group compared to the TD+ group (p < 0.05 for all).
Conclusions:
Our findings demonstrate significantly reduced parasympathetic activity (reduced HF power) and increased LF/HF (a measure of sympathovagal balance) in children with DS, together with greater exposure to hypoxia, suggesting SDB has a greater effect in these children that may contribute to an increased risk of adverse cardiovascular outcomes.
Impact:
Sleep disordered breathing in children with Down syndrome exacerbates impaired autonomic control and increases exposure to hypoxia, compared to typically developing children. In typically developing children sleep disordered breathing has adverse effects on autonomic cardiovascular control. The prevalence of sleep disordered breathing is very high in children with Down syndrome; however, studies on the effects on cardiovascular control are limited in this population. This study supports screening and early treatment of sleep disordered breathing in children with Down syndrome.
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