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Published on: December 6, 2016
Pathological Endotypic Traits of Paediatric Obstructive Sleep Apnea: Age and Sex Differences
Chien-Heng Lin1,2, Liang-Wen Hang3,4, Eysteinn Finnsson5
1Department of Pediatric Pulmonology and Critical Care Medicine, China Medical University Children's Hospital, Taichung, Taiwan.
Insights
In children with obstructive sleep apnea (OSA), poor airway compensation and collapsibility contribute to higher apnea-hypopnea index (AHI). Older children show reduced upper airway function, independent of AHI severity.
Area of Science:
- Pediatric Sleep Medicine
- Respiratory Physiology
- Otolaryngology
Background:
- Pediatric obstructive sleep apnea (OSA) has unique characteristics compared to adult OSA.
- Endotypic traits in children with OSA are not well-documented.
- Understanding age and sex variations in OSA endotypes can inform respiratory development insights.
Purpose of the Study:
- To investigate the association between age and sex with endotypic traits in pediatric OSA.
- To identify key endotypic drivers of OSA severity in children.
Main Methods:
- Prospective enrollment of 88 pediatric patients (≤18 years) with OSA (AHI ≥ 1/h).
- In-laboratory polysomnography to assess endotypic traits.
- Linear regression analysis to correlate endotypes with AHI, age, and sex.
Main Results:
- Poor compensation and worse upper airway collapsibility were linked to higher AHI.
- Compensation explained the largest variance (12.85%) in AHI.
- Older children (>12 years) had compromised upper airway function and higher loop gain, irrespective of AHI.
- No significant sex-based differences in endotypic traits were found.
Conclusions:
- Inadequate dilator muscle compensatory activity and upper airway collapsibility are significant contributors to pediatric OSA severity.
- Age-related decline in upper airway patency may involve craniofacial and airway development interactions.
Background And Objective:
Paediatric obstructive sleep apnea (OSA) has a distinct pathophysiology and management from that of adults, yet endotypic traits in this population remain underreported. Understanding how these traits vary by age and sex could provide insights into respiratory system development. This study aims to examine the association of age and sex with endotypic traits in children and adolescents with OSA.
Methods:
Between April 2020 and September 2024, we prospectively enrolled 88 patients aged ≤ 18 years who were referred to a single clinical sleep center in Taiwan for in-laboratory diagnostic polysomnography. Patients with an apnea-hypopnea index (AHI) ≥ 1 h-1 were included. Endotypic traits were estimated using polysomnographic signals. Linear regression analysis was performed to assess the associations of endotypic traits with AHI, age, and sex.
Results:
Poor compensation, worse collapsibility, and high loop gain were associated with higher AHI, with compensation explaining the largest variance (12.85%) among all endotypic traits. Patients older than 12 years exhibited a more compromised upper airway (V min: 64.3 vs. 71.4% eupnea) and higher loop gain (LG1: 0.45 vs. 0.34) than younger patients, independent of AHI. No significant sex differences in endotypic traits were observed.
Conclusions:
In addition to upper airway collapsibility, inadequate compensatory activity of the dilator muscles significantly contributed to higher AHI in paediatric patients with OSA. The age-related decrease in upper airway patency may result from the interplay between upper airway and craniofacial development.
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