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Published on: December 6, 2016
Circulating branched-chain amino acids in children with obstructive sleep apnea
Antonia Barceló1,2,3, Josep Miquel Bauça1,2, José Antonio Peña-Zarza4
1Servei Anàlisis Clíniques, Hospital Universitari Son Espases, Palma de Mallorca, Spain.
Insights
Obstructive sleep apnea (OSA) in children is linked to higher branched-chain amino acid (BCAA) levels, suggesting BCAAs may indicate insulin resistance. This highlights a new connection between sleep apnea and metabolic health.
Area of Science:
- Pediatric Endocrinology
- Sleep Medicine
- Metabolic Research
Background:
- Obstructive sleep apnea (OSA) effects on children's metabolic systems are unclear.
- Branched-chain amino acids (BCAAs) may modulate insulin action and link glucose and amino acid pathways.
Purpose of the Study:
- To investigate plasma BCAA levels as potential biomarkers for insulin resistance and metabolic dysfunction in children with OSA.
- To explore the relationship between OSA, sleep fragmentation, and BCAA metabolism in pediatric populations.
Main Methods:
- Polysomnography used for OSA diagnosis in 90 snoring children.
- Collected anthropometric, clinical, and blood samples for glucose, insulin, HbA1c, and amino acid measurements.
Main Results:
- Children with OSA exhibited significantly higher BCAA levels (leucine, isoleucine, total BCAAs) compared to controls.
- Positive correlations found between insulin levels and leucine/isoleucine.
- OSA presence associated with BCAA concentrations; arousal index linked to leucine, valine, and total BCAAs.
Conclusions:
- OSA and sleep fragmentation may alter BCAA metabolism in children, independent of obesity.
- Findings suggest a novel mechanism linking OSA to glucose homeostasis in children.
Introduction:
The effects of obstructive sleep apnea (OSA) on the metabolic system are not well understood, especially in children. Recent studies have provided evidence of the modulation of insulin action by branched-chain amino acids (BCAAs) and suggested novel mechanistic relationships between glucose and amino acid metabolic pathways. We hypothesized that plasma BCAA levels may serve as biomarkers of insulin resistance and metabolic dysfunction in children with OSA.
Methods:
A polysomnography was conducted for the diagnosis of OSA in 90 snoring children, in a tertiary hospital. Anthropometric and clinical data were measured and venous blood samples were collected for the measurement of plasma glucose, insulin, HbA1c, and amino acids.
Results:
Children with OSA had significantly higher levels of BCAAs (leucine, isoleucine, and total BCAAs) compared with those without OSA (P = 0.024). A positive significant correlation was observed between insulin levels and both leucine and isoleucine (r = 0.232; P < 0.05). On multivariate regression analyses, the presence of OSA was significantly associated with leucine, isoleucine, and total BCAA concentrations (P = 0.028), whereas the arousal index was associated with leucine, valine, and total BCAA levels (P = 0.037).
Conclusions:
The presence of OSA and sleep fragmentation may induce changes in branched-chain amino acid metabolism in snoring children, independently of obesity. These data may suggest a new mechanism linking OSA and glucose homeostasis.
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