A method for measuring and modeling the physiological traits causing obstructive sleep apnea

被引:197
作者
Wellman, Andrew [1 ]
Eckert, Danny J. [1 ]
Jordan, Amy S. [1 ]
Edwards, Bradley A. [1 ]
Passaglia, Chris L. [2 ]
Jackson, Andrew C. [2 ]
Gautam, Shiva [3 ]
Owens, Robert L. [1 ]
Malhotra, Atul [1 ]
White, David P. [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Sleep Med, Boston, MA 02115 USA
[2] Boston Univ, Dept Engn, Boston, MA 02215 USA
[3] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Biostat, Boston, MA 02115 USA
基金
澳大利亚国家健康与医学研究理事会;
关键词
pathophysiology of sleep apnea; loop gain; pharyngeal closing pressure; upper airway; arousal threshold; UPPER AIRWAY COLLAPSIBILITY; VENTILATORY STABILITY; LUNG-VOLUME; ACETAZOLAMIDE; MECHANISMS; AROUSAL; OXYGEN; HYPEROXIA; ANATOMY;
D O I
10.1152/japplphysiol.00972.2010
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
There is not a clinically available technique for measuring the physiological traits causing obstructive sleep apnea (OSA). Therefore, it is often difficult to determine why an individual has OSA or to what extent the various traits contribute to the development of OSA. In this study, we present a noninvasive method for measuring four important physiological traits causing OSA: 1) pharyngeal anatomy/collapsibility, 2) ventilatory control system gain (loop gain), 3) the ability of the upper airway to dilate/stiffen in response to an increase in ventilatory drive, and 4) arousal threshold. These variables are measured using a single maneuver in which continuous positive airway pressure (CPAP) is dropped from an optimum to various suboptimum pressures for 3- to 5-min intervals during sleep. Each individual's set of traits is entered into a physiological model of OSA that graphically illustrates the relative importance of each trait in that individual. Results from 14 subjects (10 with OSA) are described. Repeatability measurements from separate nights are also presented for four subjects. The measurements and model illustrate the multifactorial nature of OSA pathogenesis and how, in some individuals, small adjustments of one or another trait (which might be achievable with non-CPAP agents) could potentially treat OSA. This technique could conceivably be used clinically to define a patient's physiology and guide therapy based on the traits.
引用
收藏
页码:1627 / 1637
页数:11
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