Obstructive sleep apnea is associated with impaired insulin clearance and hepatic insulin sensitivity in paediatric
Giuseppina Rosaria Umano1, Francesca Aiello1, Giulia Rondinelli1
1Department of the Woman, the Child, and General and Specialized Surgery, University of Campania Luigi Vanvitelli, Naples, Italy.
Insights
Moderate-to-severe obstructive sleep apnea (OSA) in obese children impairs insulin clearance and hepatic insulin sensitivity, potentially explaining hyperinsulinism. This finding highlights a critical link between sleep health and metabolic dysfunction in pediatric obesity.
Area of Science:
- Pediatric Endocrinology
- Sleep Medicine
- Metabolic Disorders
Background:
- Obstructive sleep apnea (OSA) affects a significant portion of children and adolescents with obesity.
- OSA is associated with hyperinsulinism, but the underlying mechanisms are not fully understood.
- Understanding these mechanisms is crucial for managing metabolic complications in pediatric obesity.
Purpose of the Study:
- To investigate the determinants of hyperinsulinemia in pediatric patients with OSA.
- To assess insulin clearance, insulin secretion, and insulin sensitivity in children with varying degrees of OSA.
- To elucidate the relationship between OSA severity and metabolic parameters.
Main Methods:
- Seventy children with obesity and suspected OSA underwent polysomnography and a 3-hour oral glucose tolerance test (OGTT).
- Insulin secretion rate (ISR) was calculated using C-peptide deconvolution; insulin clearance and whole-body insulin sensitivity (Matsuda Index) were determined.
- Hepatic insulin resistance index (HIRI) was calculated based on early glucose and insulin levels during OGTT.
Main Results:
- Children with moderate-severe OSA exhibited reduced insulin clearance during OGTT and higher HIRI compared to those with mild OSA.
- No significant differences in basal insulin clearance, ISR, or whole-body insulin sensitivity were observed between groups.
- OSA severity correlated negatively with both fasting and OGTT insulin clearance and positively with HIRI.
Conclusions:
- Moderate-to-severe OSA in obese children is linked to impaired insulin clearance and hepatic insulin sensitivity.
- These metabolic alterations may contribute to the development of hyperinsulinism in pediatric OSA.
- The findings underscore the importance of addressing OSA in managing metabolic health in obese children.
Aims:
Obstructive sleep apnea (OSA) affects up to 40% of children and adolescents with obesity and is linked to hyperinsulinism. However, the mechanisms underpinning this association remain unclear. The study aims to assess the three key determinants of hyperinsulinemia: insulin clearance, secretion, and sensitivity in paediatric patients with OSA.
Methods:
We enrolled 70 Children with obesity and suspected OSA who performed a nocturnal polygraphy to confirm OSA diagnosis and a 3-hour OGTT to assess glucose homeostasis. Mild OSA was defined for 1 < AHI ≤ 5, moderate-severe OSA as AHI >5. Insulin secretion rate (ISR) was estimated using C-peptide deconvolution. Basal and total insulin clearance during OGTT were calculated. Whole-body insulin sensitivity was evaluated with the Matsuda Index (WBISI), while hepatic insulin resistance index (HIRI) was calculated based on the AUCs of plasma glucose and insulin during the initial 30 minutes of OGTT.
Results:
A total of 36 children had mild OSA and 34 had moderate-severe OSA. The latter group showed reduced insulin clearance during OGTT (p = 0.008) and higher HIRI (p = 0.03). Basal insulin clearance (p = 0.07), ISR (p = 0.34), beta-cell glucose sensitivity (p = 0.53), and WBISI (p = 0.56) were similar between the two groups. OSA severity negatively correlated with fasting insulin clearance (r = -0.29, p = 0.01) and OGTT insulin clearance (r = -0.32, p = 0.007) and positively correlated with HIRI (r = 0.29, p = 0.02).
Conclusion:
Moderate-severe OSA in children with obesity is associated with impaired insulin clearance and hepatic insulin sensitivity. These factors may contribute to hyperinsulinism in paediatric OSA.
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