Cardioventilatory Control in Preterm-born Children and the Risk of Obstructive Sleep Apnea

被引:25
|
作者
Domany, Keren Armoni [1 ,4 ]
Hossain, Md Monir [2 ]
Nava-Guerra, Leonardo [5 ]
Khoo, Michael C. [5 ]
McConnell, Keith [1 ]
Carroll, John L. [6 ]
Xu, Yuanfang [2 ]
DiFrancesco, Mark [3 ]
Amin, Raouf S. [1 ]
机构
[1] Univ Cincinnati, Cincinnati Childrens Hosp Med Ctr, Dept Radiol, Div Pulm Med, Cincinnati, OH USA
[2] Univ Cincinnati, Cincinnati Childrens Hosp Med Ctr, Dept Radiol, Div Biostat & Epidemiol, Cincinnati, OH USA
[3] Univ Cincinnati, Cincinnati Childrens Hosp Med Ctr, Dept Radiol, Pediat Neuroimaging Res Consortium, Cincinnati, OH USA
[4] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
[5] Univ Southern Calif, Dept Biomed Engn, Los Angeles, CA 90089 USA
[6] Univ Arkansas Med Sci, Div Pediat Pulm & Sleep Med, Little Rock, AR 72205 USA
关键词
obstructive sleep apnea; loop gain; cardiorespiratory coupling; neonatal prematurity; cluster analysis; HYPOXIC VENTILATORY RESPONSE; LOOP GAIN; DEVELOPMENTAL PLASTICITY; INTERMITTENT HYPOXIA; HYPEROXIA ALTERS; NEONATAL-RATS; CAROTID-BODY; CHEMORECEPTOR; BARORECEPTOR; INFANTS;
D O I
10.1164/rccm.201708-1700OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
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.
引用
收藏
页码:1596 / 1603
页数:8
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