Ventilatory Drive Withdrawal Rather Than Reduced Genioglossus Compensation as a Mechanism of Obstructive Sleep Apnea in REM Sleep

被引:37
作者
Messineo, Ludovico [1 ,2 ,3 ,4 ]
Eckert, Danny J. [1 ]
Taranto-Montemurro, Luigi [2 ,3 ,4 ]
Vena, Daniel [2 ,3 ,4 ]
Azarbarzin, Ali [2 ,3 ,4 ]
Hess, Lauren B. [2 ,3 ,4 ]
Calianese, Nicole [2 ,3 ,4 ]
White, David P. [2 ,3 ,4 ]
Wellman, Andrew [2 ,3 ,4 ]
Gell, Laura [2 ,3 ,4 ]
Sands, Scott A. [2 ,3 ,4 ,5 ,6 ]
机构
[1] Flinders Univ S Australia, Adelaide Inst Sleep Hlth, Bedford Pk, Adelaide, SA, Australia
[2] Harvard Univ, Brigham & Womens Hosp, Dept Med, Div Sleep & Circadian Disorders, Boston, MA 02115 USA
[3] Harvard Univ, Brigham & Womens Hosp, Dept Neurol, Div Sleep & Circadian Disorders, Boston, MA 02115 USA
[4] Harvard Univ, Harvard Med Sch, Boston, MA 02115 USA
[5] The Alfred, Cent Clin Sch, Dept Allergy Immunol & Resp Med, Melbourne, Vic, Australia
[6] Monash Univ, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
REM sleep pathogenesis; drive withdrawal; pharyngeal muscle responsiveness; REM sleep hypotonia; phasic and tonic REM sleep; DILATOR MUSCLE-ACTIVITY; UPPER-AIRWAY; NEGATIVE-PRESSURE; COLLAPSIBILITY; IDENTIFICATION; ASSOCIATION; DIAPHRAGM; SEVERITY; STATE;
D O I
10.1164/rccm.202101-0237OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: REM sleep is associated with reduced ventilation and greater obstructive sleep apnea (OSA) severity than non-REM (nREM) sleep for reasons that have not been fully elucidated. Objectives: Here, we use direct physiological measurements to determine whether the pharyngeal compromise in REM sleep OSA is most consistent with 1) withdrawal of neural ventilatory drive or 2) deficits in pharyngeal pathophysiology per se (i.e., increased collapsibility and decreased muscle responsiveness). Methods: Sixty-three participants with OSA completed sleep studies with gold standard measurements of ventilatory "drive" (calibrated intraesophageal diaphragm EMG), ventilation (oronasal "ventilation"), and genioglossus EMG activity. Drive withdrawal was assessed by examining these measurements at nadir drive (first decile of drive within a stage). Pharyngeal physiology was assessed by examining collapsibility (lowered ventilation at eupneic drive) and responsiveness (ventilation-drive slope). Mixed-model analysis compared REM sleep with nREM sleep; sensitivity analysis examined phasic REM sleep. Measurements and Main Results: REM sleep (>= 10 min) was obtained in 25 patients. Compared with drive in nREM sleep, drive in REM sleep dipped to markedly lower nadir values (first decile, estimate [95% confidence interval], -21.8% [-31.2% to -12.4%] of eupnea; P < 0.0001), with an accompanying reduction in ventilation (-25.8% [-31.8% to -19.8%] of eupnea; P< 0.0001). However, there was no effect of REM sleep on collapsibility (ventilation at eupneic drive), baseline genioglossus EMG activity, or responsiveness. REM sleep was associated with increased OSA severity (+10.1 [1.8 to 19.8] events/h), but this association was not present after adjusting for nadir drive (+4.3 [-4.2 to 14.6] events/h). Drive withdrawal was exacerbated in phasic REM sleep. Conclusions: In patients with OSA, the pharyngeal compromise characteristic of REM sleep appears to be predominantly explained by ventilatory drive withdrawal rather than by preferential decrements in muscle activity or responsiveness. Preventing drive withdrawal may be the leading target for REM sleep OSA.
引用
收藏
页码:219 / +
页数:23
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