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Updated: Aug 28, 2025

Human Circadian Phenotyping and Diurnal Performance Testing in the Real World
Published on: April 7, 2020
Preserved Sleep for the Same Level of Respiratory Disturbance in Children with Prader-Willi Syndrome
Qiming Tan1,2, Xiao Tian Tim He1, Sabrina Kang1
1Department of Pediatrics, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, AB T6G 1C9, Canada.
Insights
Children with Prader-Willi syndrome (PWS) exhibit better sleep continuity but lower oxygen saturation. Recombinant human growth hormone (rhGH) treatment did not alter respiratory parameters in PWS patients.
Area of Science:
- Pediatric Endocrinology
- Sleep Medicine
- Genetics
Background:
- Prader-Willi syndrome (PWS) is a complex genetic disorder affecting multiple systems.
- Obstructive sleep apnea (OSA) is a common comorbidity in PWS.
- Recombinant human growth hormone (rhGH) is a key treatment for PWS, but its impact on sleep is debated.
Purpose of the Study:
- To compare polysomnography (PSG) findings in children with and without PWS.
- To evaluate the effect of rhGH treatment on respiratory parameters in children with PWS.
Main Methods:
- Retrospective, single-center study comparing PSG data.
- Analysis of children with PWS (n=29) versus matched controls (n=87).
- Assessment of respiratory parameters before and after rhGH initiation in a subset of PWS patients (n=11).
Main Results:
- Children with PWS showed improved sleep continuity (longer total sleep time, higher sleep efficiency, fewer arousals) compared to controls.
- Lower mean oxygen saturation was observed in PWS children.
- No significant changes in polysomnography parameters were detected after rhGH treatment in PWS patients.
Conclusions:
- Children with PWS have distinct sleep patterns, including better sleep continuity and lower oxygen saturation.
- rhGH treatment in PWS does not appear to negatively impact respiratory parameters or worsen OSA.
- Further research is needed to fully understand the complex interplay between PWS, sleep, and growth hormone therapy.
Abstract:
Debate remains as to how to balance the use of recombinant human growth hormone (rhGH) as an important treatment in Prader-Willi syndrome (PWS) with its potential role in obstructive sleep apnea. This single-center, retrospective study assessed differences in overnight polysomnography results between children with and without PWS and changes in respiratory parameters before and after the initiation of rhGH treatment in those with PWS. Compared with age-, sex-, and body-mass-index-matched controls (n = 87), children with PWS (n = 29) had longer total sleep time (434 ± 72 vs. 365 ± 116 min; p < 0.01), higher sleep efficiency (86 ± 7 vs. 78 ± 15%; p < 0.05), and lower arousal events (8.1 ± 4.5 vs. 13.0 ± 8.9 events/h; p < 0.05). Mean oxygen saturation was lower in PWS children (94.3 ± 6.0 vs. 96.0 ± 2.0%; p < 0.05), with no other differences in respiratory parameters between groups. Eleven children with PWS (38%) met the criteria for further analyses of the impact of rhGH; polysomnography parameters did not change with treatment. Compared with other children undergoing polysomnography, children with PWS had more favorable markers of sleep continuity and lower oxygen saturation for the same level of respiratory disturbance. rhGH administration was not associated with changes in respiratory parameters in PWS.
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