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Published on: December 6, 2016
Obstructive sleep apnoea in children with Down syndrome
1Department of Paediatrics, Kwong Wah Hospital, Waterloo Road, Kowloon, Hong Kong. dkkng@ha.org.hk
Insights
Children with Down syndrome (DS) have a high prevalence of obstructive sleep apnoea (OSA), affecting 59%. Many DS children with OSA do not snore, highlighting the need for screening.
Area of Science:
- Pediatric Pulmonology
- Sleep Medicine
- Genetics
Background:
- Children with Down syndrome (DS) exhibit anatomical predispositions to obstructive sleep apnoea (OSA), including smaller airways and hypotonia.
- OSA is a significant concern in DS, necessitating comparative studies to understand its prevalence.
Purpose of the Study:
- To compare the prevalence of OSA in children with Down syndrome (DS) against a matched control group of children with snoring.
- To investigate the occurrence of OSA in DS children, irrespective of habitual snoring.
Main Methods:
- Prospective recruitment of DS children from the Hong Kong Down Syndrome Association.
- Polysomnography (PSG) was conducted on 22 DS children and 22 gender-, age-, and weight-for-height matched controls.
- Obstructive sleep apnoea (OSA) was defined by an apnoea-hypopnoea index (AHI) > 1.5.
Main Results:
- The prevalence of OSA was 59% in DS children versus 32% in snoring controls.
- DS children demonstrated significantly higher median AHI (1.80) compared to controls (0.50, p=0.041).
- Approximately 61.5% of DS children with OSA did not report habitual snoring.
Conclusions:
- Children with Down syndrome have a significantly higher prevalence of OSA compared to their peers.
- A substantial proportion of DS children with OSA may not present with typical snoring, underscoring the importance of PSG screening.
Introduction:
Children with Down syndrome (DS) are prone to develop obstructive sleep apnoea (OSA) for a combination of reasons, including small upper airway, midfacial hypoplasia, micrognathia and muscular hypotonia. The objective of this study was to compare the prevalence of OSA in DS children, with or without snoring, with snoring children matched for gender, age and weight for height.
Methods:
DS children were prospectively recruited from the Hong Kong Down Syndrome Association. All recruited DS children underwent a sleep polysomnography (PSG) in our sleep laboratory. The same number of patients without DS who underwent sleep PSG in the same period were enrolled as controls after they were matched for gender, age and weight for height. OSA was defined as apnoea-hypopnoea index (AHI) greater than 1.5.
Results:
22 DS patients and 22 snoring controls completed the overnight PSG. The mean age of DS children and snoring controls was 10.82 +/- 5.93 and 10.27 +/- 5.68 years, respectively. The prevalence of OSA was 59 percent in DS children and 32 percent in snoring controls. Median and interquartile range (IQR) of AHI of DS children (median 1.80, IQR is 0.40 to 7.10) were significantly higher than those of controls (median 0.50, IQR is 0.00 to 2.03, p-value equals 0.041). Out of 13 DS children with OSA, eight of them (61.5 percent) had no habitual snoring.
Conclusion:
59 percent of DS children in the current series were found to have OSA and they were more likely to develop OSA than controls. Nearly 40 percent of DS children with OSA did not have habitual snoring.
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