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Sleep spindles are reduced in children with Down syndrome and sleep-disordered breathing
Marisha Shetty1, Margot J Davey1,2, Gillian M Nixon1,2
1Department of Paediatrics, Monash University, Melbourne, VIC, Australia.
Insights
Children with Down syndrome have reduced sleep spindle activity, impacting sleep quality and daytime function. This finding may help identify risks for future cognitive decline.
Area of Science:
- Neuroscience
- Pediatrics
- Sleep Medicine
Background:
- Children with Down syndrome (DS) face a higher risk of sleep-disordered breathing (SDB).
- Sleep quality is crucial for daytime functioning, and sleep spindles are key indicators.
- This study examines sleep spindle activity in children with DS and its link to daytime function.
Purpose of the Study:
- To compare sleep spindle activity between children with DS and typically developing (TD) children.
- To investigate the relationship between sleep spindle activity and daytime functioning in children with DS.
- To explore sleep spindle activity as a potential biomarker for SDB-related issues in DS.
Main Methods:
- Overnight polysomnography was conducted on 44 children with DS and SDB, and matched TD children.
- Sleep spindles (Fast, Slow, or combined) were manually identified and quantified (number, density, intensity) at central and frontal electrodes.
- Parent-reported behavioral and sleep-related quality of life data were collected using the Child Behavior Check List and OSA-18.
Main Results:
- Children with DS exhibited significantly lower frontal (F) slow and combined (F Slow&Fast) sleep spindle activity compared to TD controls.
- No significant correlations were found between spindle activity and Child Behavior Check List subscales.
- Reduced central (C) Fast and combined (C Slow&Fast) spindle activity correlated negatively with emotional symptoms, caregiver concerns, and daytime function as per OSA-18.
Conclusions:
- Reduced sleep spindle activity in children with DS may contribute to sleep disruption and impaired daytime functioning.
- These findings highlight sleep spindles as a potential biomarker for sleep quality and associated challenges in Down syndrome.
- Further research may explore the link between reduced spindle activity and long-term cognitive health in children with DS.
Background:
Children with Down syndrome (DS) are at increased risk of sleep-disordered breathing (SDB). We investigated sleep spindle activity, as a marker of sleep quality, and its relationship with daytime functioning in children with DS compared to typically developing (TD) children.
Methods:
Children with DS and SDB (n = 44) and TD children matched for age, sex and SDB severity underwent overnight polysomnography. Fast or Slow sleep spindles were identified manually during N2/N3 sleep. Spindle activity was characterized as spindle number, density (number of spindles/h) and intensity (density × average duration) on central (C) and frontal (F) electrodes. Parents completed the Child Behavior Check List and OSA-18 questionnaires.
Results:
In children with DS, spindle activity was lower compared to TD children for F Slow and F Slow&Fast spindles combined (p < 0.001 for all). Furthermore, there were no correlations between spindle activity and CBCL subscales; however, spindle activity for C Fast and C Slow&Fast was negatively correlated with OSA-18 emotional symptoms and caregiver concerns and C Fast activity was also negatively correlated with daytime function and total problems.
Conclusions:
Reduced spindle activity in children with DS may underpin the increased sleep disruption and negative effects of SDB on quality of life and behavior.
Impact:
Children with Down syndrome (DS) are at increased risk of sleep-disordered breathing (SDB), which is associated with sleep disruption affecting daytime functioning. Sleep spindles are a sensitive marker of sleep quality. We identified for the first time that children with DS had reduced sleep spindle activity compared to typically developing children matched for SDB severity. The reduced spindle activity likely underpins the more disrupted sleep and may be associated with reduced daytime functioning and quality of life and may also be an early biomarker for an increased risk of developing dementia later in life in children with DS.
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