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Inflammation and sleep disordered breathing in children: a state-of-the-art review
1Department of Pediatrics, Soroka University Medical Center, Ben-Gurion University of the Negev, Beer-Sheva, Israel. avivgold@bgu.ac.il
Insights
Inflammation plays a key role in pediatric obstructive sleep apnea syndrome (OSAS), impacting neurobehavioral and cognitive health. Anti-inflammatory treatments show promise for mild OSAS cases, warranting further research.
Area of Science:
- Pediatric Pulmonology
- Sleep Medicine
- Immunology
Background:
- Sleep disordered breathing (SDB), including obstructive sleep apnea syndrome (OSAS), affects children's sleep and health.
- OSAS in children is linked to neurobehavioral, cognitive, and cardiovascular issues.
- Inflammation is implicated in OSAS pathophysiology and its associated morbidities.
Purpose of the Study:
- To review the role of inflammation in pediatric OSAS pathophysiology.
- To explore potential therapeutic implications of targeting inflammation in pediatric OSAS.
Main Methods:
- Review of existing literature on inflammation in pediatric OSAS.
- Analysis of studies on adenotonsillectomy and anti-inflammatory treatments for pediatric OSAS.
Main Results:
- Inflammatory changes are observed in the upper airways of children with OSAS.
- Systemic inflammation markers (e.g., hsCRP) decrease after adenotonsillectomy.
- Anti-inflammatory treatments improved symptoms and respiratory values in mild pediatric OSAS.
Conclusions:
- Inflammation is a significant factor in pediatric OSAS.
- Further research is needed to clarify the role of inflammatory markers and anti-inflammatory treatments in diagnosis and management.
Abstract:
Sleep disordered breathing (SDB) represents a spectrum of breathing disorders, ranging from snoring to obstructive sleep apnea syndrome (OSAS), that disrupt nocturnal respiration and sleep architecture. OSAS is a common disorder in children, with a prevalence of 2-3%. It is associated with neurobehavioral, cognitive, and cardiovascular morbidities. In children, adenotonsillectomy is the first choice for treatment and is reserved for moderate to severe OSAS, as defined by an overnight polysomnography. In adults, OSAS is the result of mechanical dysfunction of the upper airway, manifesting as severity-dependent nasal, oropharyngeal, and systemic inflammation that decrease after continuous positive airway pressure therapy. Inflammatory changes have been reported in upper airway samples from children with OSAS, and systemic inflammation, as indicated by high-sensitivity C-reactive protein (hsCRP) levels, has been shown to decrease in children with OSAS after adenotonsillectomy. Anti-inflammatory treatments for children with mild OSAS are associated with major improvements in symptoms, polysomnographic respiratory values, and radiologic measures of adenoid size. Inflammation is correlated to some extent with OSAS-related neurocognitive morbidity, but the role of inflammatory markers in the diagnosis and management of OSAS, and the role of anti-inflammatory treatments, remains to be clarified. This review examines the role of inflammation in the pathophysiology of sleep-disordered breathing in pediatric patients and the potential therapeutic implications.
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