Division of Respiratory Diseases, First Hospital of Jilin University, Changchun, Jilin, China.
Sleep. 2012 Sep 1;35(9):1257-67. doi: 10.5665/sleep.2082.
Abnormal ventilatory drive may contribute to the pathophysiology of the childhood obstructive sleep apnea syndrome (OSAS). Concomitant with the obesity epidemic, more adolescents are developing OSAS. However, few studies have specifically evaluated the obese adolescent group. The authors hypothesized that obese adolescents with OSAS would have a blunted hypercapnic ventilatory response (HCVR) while awake and blunted ventilatory responses to carbon dioxide (CO(2)) during sleep compared with obese and lean adolescents without OSAS.
CVR was measured during wakefulness. During nonrapid eye movement (NREM) and rapid eye movement (REM) sleep, respiratory parameters and genioglossal electromyogram were measured during CO(2) administration in comparison with room air in obese adolescents with OSAS, obese control study participants, and lean control study participants.
Sleep laboratory.
Twenty-eight obese patients with OSAS, 21 obese control study participants, and 37 lean control study participants.
The obese OSAS and obese control groups had a higher HCVR compared with the lean control group during wakefulness. During both sleep states, all 3 groups had a response to CO(2); however, the obese OSAS group had lower percentage changes in minute ventilation, inspiratory flow, inspiratory time, and tidal volume compared with the 2 control groups. There were no significance differences in genioglossal activity between groups.
HCVR during wakefulness is increased in obese adolescents. Obese adolescents with OSAS have blunted ventilatory responses to CO(2) during sleep and do not have a compensatory prolongation of inspiratory time, despite having normal CO(2) responsivity during wakefulness. Central drive may play a greater role than upper airway neuromotor tone in adapting to hypercapnia.
异常的通气驱动可能是儿童阻塞性睡眠呼吸暂停综合征(OSAS)的病理生理学基础。肥胖症的流行,使更多的青少年患有 OSAS。然而,很少有研究专门评估肥胖青少年群体。作者假设肥胖青少年 OSAS 患者在清醒时会出现高碳酸血症通气反应(HCVR)迟钝,并且与无 OSAS 的肥胖和瘦青少年相比,在睡眠期间对二氧化碳(CO2)的通气反应迟钝。
在清醒时测量 CVR。在非快速眼动(NREM)和快速眼动(REM)睡眠期间,在肥胖 OSAS 青少年、肥胖对照组参与者和瘦对照组参与者中,在给予 CO2 与吸入室内空气时,测量呼吸参数和颏舌肌肌电图。
睡眠实验室。
28 例肥胖 OSAS 患者、21 例肥胖对照组参与者和 37 例瘦对照组参与者。
在清醒时,肥胖 OSAS 和肥胖对照组的 HCVR 高于瘦对照组。在两种睡眠状态下,所有 3 组均对 CO2 有反应;然而,与 2 个对照组相比,肥胖 OSAS 组的分钟通气量、吸气流量、吸气时间和潮气量的变化百分比较低。各组颏舌肌活动无显著差异。
肥胖青少年在清醒时的 HCVR 增加。肥胖 OSAS 青少年在睡眠时对 CO2 的通气反应迟钝,尽管在清醒时对 CO2 有正常反应,但没有吸气时间的代偿延长。中枢驱动力在适应高碳酸血症方面的作用可能大于上气道神经运动张力。