疑似阻塞性睡眠呼吸暂停和阻塞性肺病患者的生物标志物:多导睡眠图、人口统计学和肺活量测定参数之间的关系

Aditi S. Shah, R. Jen, I. Laher, J. Leung, A. Allen, Stephan Van Eden, N. Ayas
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引用次数: 0

摘要

目的:本研究的目的是表征疑似阻塞性睡眠呼吸暂停(OSA)和/或阻塞性气道疾病患者的炎症和氧化应激生物标志物、人口统计学、多导睡眠图和肺活量测定参数之间的相关性。方法:这是一项横断面探索性研究,研究对象是到不列颠哥伦比亚大学睡眠诊所就诊的患者,这些患者有疑似OSA的多导睡眠图诊断。所有患者均采集样本检测IL-10、IL-6、e-选择素、内皮抑素、VCAM-1、ICAM-1、PDGF、血栓反应蛋白-2、8-OHdG、8-异前列腺素和超氧化物歧化酶。使用Spearman相关和多元线性回归来确定生物标志物的预测因子。结果:共纳入63例患者:男性占65%,平均年龄53岁,体重指数(BMI) 33 kg/m2。炎症生物标志物与女性(IL-6,系数0.51,p = 0.032)、FEV1 (IL-6,系数- 0.02,p = 0.013)和BMI (VCAM-1,系数0.009,p = 0.051)相关。氧化应激标志物8-OHdG与快速眼动(REM)睡眠低氧血症相关(系数0.006,p = 0.02)。年龄和BMI均与SpO2低于90%的时间百分比独立相关。快速眼动睡眠和OSA重叠患者的快速眼动和非快速眼动(NREM)睡眠低氧血症程度高于对照组。最后,对照组、OSA、阻塞性气道疾病和重叠组之间的氧化或炎症生物标志物没有差异,尽管每组的患者数量都很小。结论:女性、FEV1较低和BMI升高是炎症生物标志物水平升高的独立预测因素。氧化应激标志物8-OHdG与REM低氧血症指数相关。有必要进行更大规模的研究,以描绘重叠条件下患者的生物标志物谱。
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Biomarkers in patients with suspected obstructive sleep apnea and obstructive lung disease: Associations among polysomnographic, demographic and spirometric parameters
Abstract PURPOSE: The purpose of this study was to characterize the associations between inflammatory and oxidative stress biomarkers, demographic, polysomnographic and spirometric parameters in patients with suspected obstructive sleep apnea (OSA) and/or obstructive airway disease. METHODS: This was a cross-sectional exploratory study of patients referred to the University of British Columbia Sleep Clinic who had a diagnostic polysomnogram for suspected OSA. All patients had samples collected for measurements of IL-10, IL-6, e-selectin, endostatin, VCAM-1, ICAM-1, PDGF, thrombospondin-2, 8-OHdG, 8-isoprostane and superoxide dismutase. Spearman correlation and multiple linear regression were used to identify predictors of biomarkers. RESULTS: A total of 63 patients were included: 65% male, mean age 53 years and body mass index (BMI) 33 kg/m2. Inflammatory biomarkers were associated with female sex (IL-6, coefficient 0.51, p = 0.032), FEV1 (IL-6, coefficient −0.02, p = 0.013) and BMI (VCAM-1, coefficient 0.009, p = 0.051). The oxidative stress marker, 8-OHdG, was associated with hypoxemia in rapid eye movement (REM) sleep (coefficient 0.006, p = 0.02). Age and BMI were both independently associated with percentage of time spent below SpO2 90%. REM sleep and patients with overlap conditions and OSA had greater degree of REM and nonrapid eye movement (NREM) sleep hypoxemia than control group. Lastly, there were no differences in oxidative or inflammatory biomarkers between control, OSA, obstructive airway disease and overlap groups though the number of patients in each group were small. CONCLUSION: Female sex, lower FEV1 and increased BMI were independent predictors of increased inflammatory biomarker levels. The oxidative stress marker 8-OHdG was associated with hypoxemia indices of REM. Larger studies are warranted to delineate biomarker profiles in patients with overlap conditions.
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12.50%
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51
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