Quantifying the Arousal Threshold Using Polysomnography in Obstructive Sleep Apnea

被引:127
|
作者
Sands, Scott A. [1 ,2 ,3 ,4 ]
Terrill, Philip I. [5 ]
Edwards, Bradley A. [1 ,2 ,6 ,7 ,8 ]
Montemurro, Luigi Taranto [1 ,2 ]
Azarbarzin, Ali [1 ,2 ]
Marques, Melania [1 ,2 ,9 ]
de Melo, Camila M. [1 ,2 ]
Loring, Stephen H. [2 ,10 ]
Butler, James P. [1 ,2 ]
White, David P. [1 ,2 ]
Wellman, Andrew [1 ,2 ]
机构
[1] Brigham & Womens Hosp, Div Sleep & Circadian Disorders, Boston, MA USA
[2] Harvard Med Sch, Boston, MA USA
[3] Alfred & Monash Univ, Dept Allergy Immunol & Resp Med, Melbourne, Vic, Australia
[4] Alfred & Monash Univ, Cent Clin Sch, Melbourne, Vic, Australia
[5] Univ Queensland, Sch Informat Technol & Elect Engn, Brisbane, Qld, Australia
[6] Monash Univ, Dept Physiol, Sleep & Circadian Med Lab, Melbourne, Vic, Australia
[7] Monash Univ, Sch Psychol Sci, Melbourne, Vic, Australia
[8] Monash Univ, Monash Inst Cognit & Clin Neurosci, Melbourne, Vic, Australia
[9] Univ Sao Paulo, Hosp Clin, Sch Med, Heart Inst InCor,Pulm Div, Sao Paulo, Brazil
[10] Beth Israel Deaconess Med Ctr, Dept Anesthesia & Crit Care, Boston, MA 02215 USA
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
arousability; pathophysiology; personalized medicine; endotype; PHYSIOLOGICAL TRAITS; SLOW-WAVE; VENTILATORY INSTABILITY; MUSCLE RESPONSIVENESS; GENIOGLOSSUS ACTIVITY; RESPIRATORY EFFORT; LUNG-VOLUME; AIRWAY; PRESSURE; EVENTS;
D O I
10.1093/sleep/zsx183
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study Objectives: Precision medicine for obstructive sleep apnea (OSA) requires noninvasive estimates of each patient's pathophysiological "traits." Here, we provide the first automated technique to quantify the respiratory arousal threshold-defined as the level of ventilatory drive triggering arousal from sleep-using diagnostic polysomnographic signals in patients with OSA. Methods: Ventilatory drive preceding clinically scored arousals was estimated from polysomnographic studies by fitting a respiratory control model (Terrill et al.) to the pattern of ventilation during spontaneous respiratory events. Conceptually, the magnitude of the airflow signal immediately after arousal onset reveals information on the underlying ventilatory drive that triggered the arousal. Polysomnographic arousal threshold measures were compared with gold standard values taken from esophageal pressure and intraoesophageal diaphragm electromyography recorded simultaneously (N = 29). Comparisons were also made to arousal threshold measures using continuous positive airway pressure (CPAP) dial-downs (N = 28). The validity of using (linearized) nasal pressure rather than pneumotachograph ventilation was also assessed (N = 11). Results: Polysomnographic arousal threshold values were correlated with those measured using esophageal pressure and diaphragm EMG (R = 0.79, p < .0001; R = 0.73, p = .0001), as well as CPAP manipulation (R = 0.73, p < .0001). Arousal threshold estimates were similar using nasal pressure and pneumotachograph ventilation (R = 0.96, p < .0001). Conclusions: The arousal threshold in patients with OSA can be estimated using polysomnographic signals and may enable more personalized therapeutic interventions for patients with a low arousal threshold.
引用
收藏
页数:9
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