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Sleep-Related Rhythmic Movement Disorder in Young Children with Down Syndrome: Prevalence and Clinical Features
Ceren Kose1, Izabelle Wood1, Amy Gwyther1
1School of Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
Insights
Sleep-related Rhythmic Movement Disorder (RMD) is common in children with Down syndrome (DS), affecting sleep quality. Screening for RMD in children with DS is recommended as it is treatable.
Area of Science:
- Neurology
- Pediatrics
- Sleep Medicine
Background:
- Sleep-related Rhythmic Movement Disorder (RMD) affects 1% of UK pre-schoolers.
- Limited data exists on RMD prevalence in children with Down syndrome (DS).
Purpose of the Study:
- Determine RMD prevalence in children with DS (ages 1.5-8 years).
- Compare phenotypic and sleep quality differences between DS children with and without RMD.
- Assess night-to-night variability of rhythmic movements (RMs).
Main Methods:
- Utilized a DS research registry to identify potential RMD cases.
- Confirmed RMD using home video-somnography (3 nights).
- Assessed sleep quality via actigraphy (5 nights) and explored phenotype with questionnaires.
Main Results:
- Confirmed RMD in 8 children; estimated prevalence ranged from 4.10% to 15.38%.
- Children with DS and RMD exhibited significantly lower sleep efficiency (69.1%) vs. controls (85.2%).
- No significant daytime phenotypic differences were observed between RMD cases and controls.
Conclusions:
- RMD is highly prevalent in children with DS, associated with poor sleep quality, and shows night-to-night variability.
- No significant daytime phenotypic differences were found in this small sample.
- Routine screening for RMD in children with DS is advised due to its treatable nature.
Abstract:
Sleep-related Rhythmic Movement Disorder (RMD) affects around 1% of UK pre-school children. Little is known about RMD in Down syndrome (DS). We aimed to determine: (a) the prevalence of RMD in children with DS aged 1.5-8 years; (b) phenotypic and sleep quality differences between children with DS and RMD and sex- and age-matched DS controls; and (c) night-to-night variability in rhythmic movements (RMs). Parents who previously reported RMs from a DS research registry of 202 children were contacted. If clinical history suggested RMD, home videosomnography (3 nights) was used to confirm RMs and actigraphy (5 nights) was used to assess sleep quality. Phenotype was explored by demographic, strengths and difficulties, Q-CHAT-10/social communication and life events questionnaires. Eight children had confirmed RMD. Minimal and estimated maximal prevalence were 4.10% and 15.38%, respectively. Sleep efficiency was significantly lower in RMD-cases (69.1%) versus controls (85.2%), but there were no other phenotypic differences. There was considerable intra-individual night-to-night variability in RMs. In conclusion, RMD has a high prevalence in children with DS, varies from night to night and is associated with poor sleep quality but, in this small sample, no daytime phenotypic differences were found compared to controls. Children with DS should be screened for RMD, which is amenable to treatment.
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