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Pathophysiology Underlying Demographic and Obesity Determinants of Sleep Apnea Severity.人口统计学和肥胖决定睡眠呼吸暂停严重程度的病理生理学基础。
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Variability in the response to atomoxetine and oxybutynin for OSA: Highlighting the need for personalized medicine.对于阻塞性睡眠呼吸暂停(OSA),托莫西汀和奥昔布宁反应的变异性:凸显个性化医疗的必要性。
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阻塞性睡眠呼吸暂停患者中肥胖和睡眠相关通气不足的内型特征

Endotypic Traits Characterizing Obesity and Sleep-related Hypoventilation in Patients with Obstructive Sleep Apnea.

作者信息

Hang Liang-Wen, Liang Shinn-Jye, Finnsson Eysteinn, Ágústsson Jón S, Sands Scott A, Cheng Wan-Ju

机构信息

College of Medicine and.

Sleep Medicine Center, Department of Pulmonary and Critical Care Medicine, and.

出版信息

Ann Am Thorac Soc. 2025 May;22(5):749-756. doi: 10.1513/AnnalsATS.202407-752OC.

DOI:10.1513/AnnalsATS.202407-752OC
PMID:39626220
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12051927/
Abstract

Sleep-related hypoventilation disorder (SHD) is common among obese patients with obstructive sleep apnea (OSA), but the pathological endotypes associated with obesity and SHD remain unclear. To investigate the relationship between endotypes with body mass index (BMI) among patients with OSA and to explore endotypic traits of patients with comorbid SHD. We prospectively collected polysomnographic studies of 1,364 patients with OSA and overnight transcutaneous CO measurements among 420 obese patients. Endotypic traits were estimated using polysomnographic signals. SHD was determined using transcutaneous CO > 55 mm Hg for ⩾10 minutes. We illustrated the nonlinear relationship between BMI and endotypic traits. Differences in endotypic traits between nonobese patients with OSA, obese patients with simple OSA, and obese patients with comorbid OSA and SHD were examined using Kruskal-Wallis tests and multiple regression analysis. A unit increase in BMI was associated with a 1.02%eupnea increase in arousal threshold, 1.16%eupnea increase in collapsibility, 0.01 increase in loop gain, and 0.48%eupnea increase in compensation, with a ceiling effect. SHD was observed in 18-36% of obese patients with OSA, depending on the criteria. Among obese patients with OSA, those with SHD exhibited a 0.06 higher loop gain than those with simple OSA, after adjusting for BMI. A ceiling effect of upper airway compensation function coupled with worse collapsibility and high loop gain characterizes pathological endotypes of obese patients with OSA. Patients with SHD exhibited a more sensitive respiratory pattern, indicated by increased loop gain.

摘要

睡眠相关通气不足障碍(SHD)在患有阻塞性睡眠呼吸暂停(OSA)的肥胖患者中很常见,但与肥胖和SHD相关的病理内型仍不清楚。为了研究OSA患者内型与体重指数(BMI)之间的关系,并探索合并SHD患者的内型特征。我们前瞻性地收集了1364例OSA患者的多导睡眠图研究数据以及420例肥胖患者的夜间经皮二氧化碳测量数据。使用多导睡眠图信号估计内型特征。当经皮二氧化碳≥55 mmHg持续≥10分钟时确定为SHD。我们阐述了BMI与内型特征之间的非线性关系。使用Kruskal-Wallis检验和多元回归分析检查非肥胖OSA患者、单纯肥胖OSA患者以及合并OSA和SHD的肥胖患者在内型特征上的差异。BMI每增加一个单位,觉醒阈值的平静呼吸增加1.02%,塌陷性的平静呼吸增加1.16%,环路增益增加0.01,代偿的平静呼吸增加0.48%,存在天花板效应。根据标准,在18%至36%的肥胖OSA患者中观察到SHD。在肥胖OSA患者中,校正BMI后,合并SHD的患者比单纯OSA患者的环路增益高0.06。上气道代偿功能的天花板效应、更差的塌陷性和高环路增益是肥胖OSA患者病理内型的特征。合并SHD的患者表现出更敏感的呼吸模式,表现为环路增益增加。