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Inflammatory Factors: Nonobese Pediatric Obstructive Sleep Apnea and Adenotonsillectomy
Yu-Shu Huang1, Wei-Chih Chin1, Christian Guilleminault2
1Department of Child Psychiatry and Sleep Center, Chang Gung Memorial Hospital and College of Medicine, Taoyuan, Taiwan.
Insights
Pediatric obstructive sleep apnea (OSA) involves inflammation. Adenotonsillectomy (T&A) improved OSA symptoms and inflammation markers, but persistent high IL-23 and HS-CRP indicate ongoing issues.
Area of Science:
- Pediatric pulmonology
- Sleep medicine
- Immunology
Background:
- Pediatric obstructive sleep apnea (OSA) is linked to inflammation.
- Cytokines like IL-17 and IL-23 are implicated in OSA.
- The study investigates inflammatory markers before and after adenotonsillectomy (T&A) in children with OSA.
Purpose of the Study:
- To evaluate the impact of T&A on inflammatory markers in children with OSA.
- To compare cytokine levels in children with OSA to controls.
- To identify potential biomarkers for persistent sleep-disordered breathing after T&A.
Main Methods:
- Prospective follow-up of 55 children (ages 4-12) with OSA undergoing T&A.
- Polysomnography (PSG), blood tests (HS-CRP, TNF-α, IL-1, 6, 10, 12, 17, 23), and questionnaires administered pre- and post-T&A.
- Comparison with 32 age-matched controls.
Main Results:
- T&A significantly improved OSA symptoms, AHI, and oxygen saturation.
- Children with OSA had higher baseline cytokine levels than controls.
- Post-T&A, significant reductions were observed in HS-CRP, TNF-α, IL-1β, IL-10, and IL-17.
- Persistent abnormal AHI correlated with unnormalized IL-23 and HS-CRP levels.
Conclusions:
- Sleep-disordered breathing can persist post-T&A, maintaining a negative inflammatory effect.
- High-sensitivity C-reactive protein (HS-CRP) and IL-23 may indicate persistent sleep-disordered breathing after T&A.
- Monitoring these markers could aid in managing residual OSA.
Background:
Inflammation is often considered relating to pediatric obstructive sleep apnea (OSA). We conducted a study investigating cytokines, including Il-17 and Il-23, in children with OSA before and after adenotonsillectomy (T&A), compared with controls.
Methods:
Children with OSA between age 4 and 12 receiving T&A were prospectively followed. Evaluation before and reevaluation six months after the treatment were done, including polysomnography (PSG), blood tests, and questionnaires. Blood samples were obtained to determine the values of high-sensitivity-C-reactive-protein (HS-CRP); tumor-necrosis-factor-alpha (TNF-α); and interleukin (IL)-1, 6, 10, 12, 17, and 23. We compared the results with an age-matched control group.
Results:
We included 55 OSA children and 32 controls. Children with OSA presented significant improvement after T&A in complaints, signs, apnea hypopnea index (AHI) (p < 0.001), mean oxygen desaturation index (p < 0.001), and mean oxygen saturation (p = 0.010). Upon entering this study, children with OSA had significantly higher cytokine levels than the controls and significant changes in HS-CRP (p = 0.013), TNF-α (p = 0.057), IL-1β (p = 0.022), IL-10 (p = 0.035), and IL-17 (p = 0.010) after T&A. Children with improved but persistently abnormal AHI did not have all cytokine levels normalized, particularly IL-23 and HS-CRP.
Conclusion:
Sleep-disordered breathing can persist after T&A and can continue to have a negative inflammatory effect. HS-CRP and IL-23 may serve as blood markers for the persistence of sleep-disordered breathing after T&A.
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