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Published on: December 6, 2016
Cardioventilatory Control in Preterm-born Children and the Risk of Obstructive Sleep Apnea
Keren Armoni Domany1,2, Md Monir Hossain3, Leonardo Nava-Guerra4
11 Division of Pulmonary Medicine.
Insights
Ventilatory control phenotypes in preterm-born children predict obstructive sleep apnea (OSA) risk. Identifying these patterns can help personalize care for children susceptible to OSA.
Area of Science:
- Pediatric Pulmonology
- Sleep Medicine
- Neurodevelopmental Pediatrics
Background:
- Obstructive sleep apnea (OSA) is a significant concern in preterm-born children, yet the role of ventilatory control in its pathogenesis remains unclear.
- Understanding ventilatory control mechanisms is crucial for identifying children at higher risk of developing OSA.
Purpose of the Study:
- To characterize distinct phenotypes of ventilatory control associated with OSA in early childhood among preterm-born children.
- To identify specific ventilatory control parameters that can stratify OSA risk in this population.
Main Methods:
- Children born preterm and at term without comorbidities were enrolled and categorized into OSA and non-OSA groups based on polysomnography.
- Ventilatory instability (loop gain, controller gain, plant gain) and brainstem maturation (cardiorespiratory coupling) were assessed.
- Cluster analysis identified phenotypes based on controller gain, plant gain, cardiorespiratory coupling, and gestational age.
Main Results:
- Three distinct ventilatory control phenotypes were identified, with OSA risks of 8%, 47%, and 77%.
- A stepwise decrease in controller gain and increase in plant gain were observed across clusters, correlating with increased OSA risk.
- Higher cardiorespiratory coupling and gestational age were associated with lower OSA risk phenotypes.
Conclusions:
- Ventilatory control parameters, including controller gain, plant gain, cardiorespiratory coupling, and gestational age, can effectively stratify OSA risk in preterm-born children.
- These findings support the development of personalized care strategies for children at risk of obstructive sleep apnea.
Rationale:
The contribution of ventilatory control to the pathogenesis of obstructive sleep apnea (OSA) in preterm-born children is unknown.
Objectives:
To characterize phenotypes of ventilatory control that are associated with the presence of OSA in preterm-born children during early childhood.
Methods:
Preterm- and term-born children without comorbid conditions were enrolled. They were categorized into an OSA group and a non-OSA group on the basis of polysomnography.
Measurements And Main Results:
Loop gain, controller gain, and plant gain, reflecting ventilatory instability, chemoreceptor sensitivity, and blood gas response to a change in ventilation, respectively, were estimated from spontaneous sighs identified during polysomnography. Cardiorespiratory coupling, a measure of brainstem maturation, was estimated by measuring the interval between inspiration and the preceding electrocardiogram R-wave. Cluster analysis was performed to develop phenotypes based on controller gain, plant gain, cardiorespiratory coupling, and gestational age. The study included 92 children, 63 of whom were born preterm (41% OSA) and 29 of whom were born at term (48% OSA). Three phenotypes of ventilatory control were derived with risks for OSA being 8%, 47%, and 77% in clusters 1, 2, and 3, respectively. There was a stepwise decrease in controller gain and an increase in plant gain from clusters 1 to 3. Children in cluster 1 had significantly higher cardiorespiratory coupling and gestational age than clusters 2 and 3. No difference in loop gain was found between clusters.
Conclusions:
The risk for OSA could be stratified according to controller gain, plant gain, cardiorespiratory coupling, and gestational age. These findings could guide personalized care for children at risk for OSA.
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