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Published on: December 6, 2016
Abnormalities in autonomic function in obese boys at-risk for insulin resistance and obstructive sleep apnea
Flavia M S Oliveira1, Winston H Tran2, Daniel J Lesser3
1Department of Electrical Engineering, University of Brasilia, Brasilia, Brazil. flavia@ene.unb.br.
Insights
Obstructive sleep apnea (OSA) in obese children is linked to autonomic dysfunction and impaired glucose metabolism. Metabolic dysfunction, not OSA severity, significantly impacts vascular sympathetic activity and vagal function.
Area of Science:
- Pediatric Endocrinology
- Sleep Medicine
- Cardiovascular Physiology
Background:
- Obstructive sleep apnea (OSA) is associated with autonomic dysfunction and glucose metabolism issues in adults.
- These relationships are less understood in obese children.
Purpose of the Study:
- To investigate the associations among obstructive sleep apnea (OSA), glucose metabolism, and daytime autonomic function in obese pediatric subjects.
Main Methods:
- Overnight polysomnography was performed on 23 obese boys.
- Frequently sampled intravenous glucose tolerance tests assessed glucose metabolism.
- Cardiorespiratory data were recorded in supine and standing postures to evaluate autonomic function.
Main Results:
- Insulin resistance, elevated fasting glucose, and reduced beta-cell function correlated with blood pressure and heart rate variability reactivity, independent of OSA severity.
- Reduced baroreflex sensitivity reactivity was observed with sleep fragmentation in participants with impaired insulin sensitivity.
Conclusions:
- Metabolic dysfunction, rather than OSA severity, more significantly impacts vascular sympathetic activity in obese children.
- Blunted vagal autonomic function due to sleep fragmentation in OSA is exacerbated by co-existing metabolic dysfunction.
Study Objectives:
Current evidence in adults suggests that, independent of obesity, obstructive sleep apnea (OSA) can lead to autonomic dysfunction and impaired glucose metabolism, but these relationships are less clear in children. The purpose of this study was to investigate the associations among OSA, glucose metabolism, and daytime autonomic function in obese pediatric subjects.
Methods:
Twenty-three obese boys participated in: overnight polysomnography; a frequently sampled intravenous glucose tolerance test; and recordings of spontaneous cardiorespiratory data in both the supine (baseline) and standing (sympathetic stimulus) postures.
Results:
Baseline systolic blood pressure and reactivity of low-frequency heart rate variability to postural stress correlated with insulin resistance, increased fasting glucose, and reduced beta-cell function, but not OSA severity. Baroreflex sensitivity reactivity was reduced with sleep fragmentation, but only for subjects with low insulin sensitivity and/or low first-phase insulin response to glucose.
Conclusions:
These findings suggest that vascular sympathetic activity impairment is more strongly affected by metabolic dysfunction than by OSA severity, while blunted vagal autonomic function associated with sleep fragmentation in OSA is enhanced when metabolic dysfunction is also present.
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