Borker Priya V, Reid Michelle, Sofer Tamar, Butler Matthew P, Azarbarzin Ali, Wang Heming, Wellman Andrew, Sands Scott A, Redline Susan
Department of Pulmonary, Allergy, and Critical Care Medicine and.
Center for Sleep and Cardiovascular Outcomes Research, University of Pittsburgh, Pittsburgh, Pennsylvania.
Am J Respir Crit Care Med. 2021 May 1;203(9):1173-1182. doi: 10.1164/rccm.202005-1808OC.
Symptoms and morbidities associated with obstructive sleep apnea (OSA) vary across individuals and are not predicted by the apnea-hypopnea index (AHI). Respiratory event duration is a heritable trait associated with mortality that may further characterize OSA. We evaluated how hypopnea and apnea durations in non-REM (NREM) sleep vary across demographic groups and quantified their associations with physiological traits (loop gain, arousal threshold, circulatory delay, and pharyngeal collapsibility). Data were analyzed from 1,546 participants from the Multi-Ethnic Study of Atherosclerosis with an AHI ≥5. Physiological traits were derived using a validated model fit to the polysomnographic airflow signal. Multiple linear regression models were used to evaluate associations of event duration with demographic and physiological factors. Participants had a mean age ± SD of 68.9 ± 9.2 years, mean NREM hypopnea duration of 21.73 ± 5.60, and mean NREM apnea duration of 23.87 ± 7.44 seconds. In adjusted analyses, shorter events were associated with younger age, female sex, higher body mass index ( < 0.01, all), and Black race ( < 0.05). Longer events were associated with Asian race ( < 0.01). Shorter event durations were associated with lower circulatory delay (2.53 ± 0.13 s, < 0.01), lower arousal threshold (1.39 ± 0.15 s, < 0.01), reduced collapsibility (-0.71 ± 0.16 s, < 0.01), and higher loop gain (-0.27 ± 0.11 s, < 0.05) per SD change. Adjustment for physiological traits attenuated age, sex, and obesity associations and eliminated racial differences in event duration. Average event duration varies across population groups and provides information on ventilatory features and airway collapsibility not captured by the AHI.
与阻塞性睡眠呼吸暂停(OSA)相关的症状和发病率因人而异,且无法通过呼吸暂停低通气指数(AHI)预测。呼吸事件持续时间是一种与死亡率相关的可遗传特征,可能进一步描述OSA的特征。我们评估了非快速眼动(NREM)睡眠中的低通气和呼吸暂停持续时间在不同人口统计学群体中的差异,并量化了它们与生理特征(环路增益、唤醒阈值、循环延迟和咽部可塌陷性)的关联。对来自动脉粥样硬化多民族研究的1546名AHI≥5的参与者的数据进行了分析。生理特征通过拟合多导睡眠图气流信号的经过验证的模型得出。使用多元线性回归模型评估事件持续时间与人口统计学和生理因素的关联。参与者的平均年龄±标准差为68.9±9.2岁,平均NREM低通气持续时间为21.73±5.60秒,平均NREM呼吸暂停持续时间为23.87±7.44秒。在调整分析中,较短的事件与较年轻的年龄、女性、较高的体重指数(均<0.01)和黑人种族(<0.05)相关。较长的事件与亚洲种族相关(<0.01)。每标准差变化,较短的事件持续时间与较低的循环延迟(2.53±0.13秒,<0.01)、较低的唤醒阈值(1.39±0.15秒,<0.01)、降低的可塌陷性(-0.71±0.16秒,<0.01)和较高的环路增益(-0.27±0.11秒,<0.05)相关。对生理特征进行调整后,年龄、性别和肥胖关联减弱,事件持续时间的种族差异消除。平均事件持续时间在不同人群中有所不同,并提供了AHI未捕捉到的通气特征和气道可塌陷性信息。