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Myeloid-related protein 8/14 levels in children with obstructive sleep apnoea
J Kim1, R Bhattacharjee, A B Snow
1Dept of Paediatrics, University of Chicago, Chicago, IL 60637, USA.
Insights
Myeloid-related protein (MRP) 8/14 levels are elevated in children with obstructive sleep apnoea (OSA). Higher MRP8/14 levels correlate with OSA severity and endothelial dysfunction, indicating potential cardiovascular risks.
Area of Science:
- Pediatric Sleep Medicine
- Cardiovascular Research
- Inflammatory Biomarkers
Background:
- Obstructive sleep apnoea (OSA) is prevalent in children, causing significant end-organ damage.
- Myeloid-related protein (MRP) 8/14 is implicated in atherosclerosis and endothelial dysfunction.
Purpose of the Study:
- To investigate the association between MRP8/14 levels and obstructive sleep apnoea (OSA) in children.
- To explore the relationship between MRP8/14, OSA severity, and endothelial function.
Main Methods:
- 255 children underwent sleep studies and provided morning blood samples.
- Plasma MRP8/14, interleukin-6, and C-reactive protein levels were measured.
- Endothelial function was assessed via brachial artery hyperemic response.
Main Results:
- Plasma MRP8/14 levels increased in a dose-dependent manner with the apnoea/hypopnoea index (AHI), irrespective of obesity.
- MRP8/14 levels correlated significantly with AHI and impaired endothelial function.
- Children with the highest MRP8/14 levels had significantly increased odds of mild to severe OSA.
Conclusions:
- Elevated plasma MRP8/14 levels are associated with paediatric OSA.
- MRP8/14 may serve as a biomarker for increased cardiovascular morbidity risk in children with OSA.
- Further research is needed to define the long-term cardiovascular impact of elevated MRP8/14 in paediatric OSA.
Abstract:
Obstructive sleep apnoea (OSA) is common in children and leads to multiple end-organ morbidities. Myeloid-related protein (MRP) 8/14 plays an important pathophysiological role in atherosclerosis, and plasma levels correlate with endothelial cell dysfunction. We hypothesised that MRP8/14 levels would be altered in children with OSA. 255 children (aged 7.6+/-1.5 yrs) were included after a sleep study and a morning blood sample. MRP8/14 and interleukin-6 plasma levels were assayed using ELISA and C-reactive protein by immunoturbidometry. Endothelial function was assessed as the hyperaemic response after occlusion of the brachial artery. Plasma log MRP8/14 levels showed apnoea/hypopnoea index (AHI) dose-dependent increases regardless of obesity. Moreover, log MRP8/14 levels correlated with log AHI (r = 0.340, p<0.001) after controlling for age and body mass index Z-score, and with endothelial function. Children with the highest MRP levels (>1.34 ug x mL(-1)) had 2.4- and 5.4-fold increased odds of mild OSA and moderate-to-severe OSA, respectively, after adjusting for confounding variables. Plasma MRP8/14 levels are associated with paediatric OSA and may reflect increased risk for cardiovascular morbidity. The short- and long-term consequences of elevated MRP8/14 on cardiovascular function in the context of paediatric OSA remain to be defined.
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