Longitudinal change in sleep, functional, and behavioural characteristics in a cohort of children with Down syndrome

Author:

Chawla Jasneek K.12ORCID,Bernard Anne3,Staton Sally4,Burgess Scott25,Heussler Helen126

Affiliation:

1. Department of Paediatric Respiratory and Sleep Medicine Queensland Children's Hospital Brisbane Queensland Australia

2. Child Health Research Centre, Faculty of Medicine University of Queensland Brisbane Queensland Australia

3. QCIF Bioinformatics, Institute for Molecular Bioscience University of Queensland Brisbane Queensland Australia

4. Queensland Brain Institute University of Queensland Brisbane Queensland Australia

5. Queensland Lung and Sleep Specialists Brisbane Queensland Australia

6. Child Development Department Queensland Children's Hospital Brisbane Queensland Australia

Abstract

SummaryThis paper describes the longitudinal change in sleep, functional, and behavioural characteristics in a cohort of children with Down syndrome, including the effect of sleep interventions in a subset. A prospective longitudinal cohort study was undertaken in children with Down syndrome aged 3–16 years comparing (1) children referred to a tertiary sleep medicine clinic who received sleep hygiene advice and an additional sleep treatment (DSref_I) with (2) children attending the same clinic who only received sleep hygiene advice (DSref_N) and (3) children recruited from the community who, were not receiving any treatment (DScomm). Data collected included demographic and medical history information, Child Sleep Habits Questionnaire‐Abbreviated (CSHQ‐A), Life‐Habits Questionnaire (Life‐H) and Child Behaviour Checklist (CBCL) at baseline and then 6‐monthly for a total of 18 months. Any sleep interventions during this time were recorded. A total of 57 children were included (DSref_I, n = 16; DSref_N, n = 25; DScomm, n = 16). At recruitment, the median CSHQ‐A total score was high (>41) in all three subgroups, but highest in the DSref_I subgroup (median [interquartile range] Dsref_I score 58 [53–66] versus DSref_N score 49 [43–53], p = 0.019). Although improved, 80% of participants in the DSref_I subgroup still had a CSHQ‐A total score >41 at the last assessment point. The median total Life‐H and total CBCL scores were not significantly different between groups at baseline and there was no significant time, group, or interaction effect seen through the study. Over an 18‐month period, sleep problems were seen to persist in children with Down syndrome. Treatment resulted in only modest improvements in sleep.

Funder

Queensland Government

Royal Australasian College of Physicians

Publisher

Wiley

Subject

Behavioral Neuroscience,Cognitive Neuroscience,General Medicine

Reference51 articles.

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