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Pro-atherogenic cytokine profile of patients with suspected obstructive sleep apnea.

机译:怀疑阻塞性睡眠呼吸暂停的患者的促动脉粥样硬化细胞因子概况。

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PURPOSE: Systemic inflammation is important in the pathogenesis of cardiovascular disease (CVD). We sought to characterize the systemic inflammatory profile associated with obstructive sleep apnea (OSA). METHODS: Adult patients referred for suspected OSA at the University of British Columbia Hospital Sleep Disorders Program were recruited for our study. Patients using HMG CoA inhibitors or a history of CVD were excluded. Fasting serum samples were obtained the morning after their diagnostic polysomnograms. Samples were tested for the following circulating inflammatory mediators: interferon gamma; interleukins 1B, 6, and 8; intercellular and vascular cell adhesion molecules (sICAM-1 and sVCAM-1); and leptin using a multiplex Luminex System. RESULTS: There were 176 patients; 68% were male, mean age = 50 +/- (SD) 11 years, mean apnea/hyponea index (AHI) = 22.9 +/- 22/h, mean desaturation (i.e. % of sleep time spent below an oxyhemoglobin saturation of 90%) = 5.4% +/- 15, and mean body mass index (BMI) = 32.2 +/- 8 kg/m(2). In univariate analyses, only leptin, sVCAM-1, and sICAM-1 were significantly associated with indices of OSA severity (i.e. AHI and/or desaturation). In multivariate linear regression analyses that controlled for BMI, gender, age, and current smoking; desaturation persisted as a significant independent predictor for elevated sVCAM-1 and leptin. CONCLUSIONS: We did not find significant associations between OSA and markers of activated innate immunity (IL-1B, 6, and 8). However, OSA severity was independently associated with serum levels of sVCAM-1 and leptin; these may represent mechanisms involved in the pathogenesis of OSA-related CVD.
机译:目的:全身性炎症在心血管疾病(CVD)的发病机理中很重要。我们试图表征与阻塞性睡眠呼吸暂停(OSA)相关的全身性炎症。方法:招募了在不列颠哥伦比亚大学医院睡眠障碍计划中转诊为疑似OSA的成年患者,以进行我们的研究。排除使用HMG CoA抑制剂或有CVD史的患者。诊断多导睡眠图后的第二天早晨获得空腹血清样品。对样品进行以下循环炎症介质测试:干扰素γ;白介素1B,6和8;细胞间和血管细胞粘附分子(sICAM-1和sVCAM-1);和瘦蛋白使用多重Luminex系统。结果:176例患者。 68%是男性,平均年龄= 50 +/-(SD)11岁,平均呼吸暂停/呼吸不足指数(AHI)= 22.9 +/- 22 / h,平均不饱和度(即,在氧合血红蛋白饱和度低于90时所花费的睡眠时间百分比%)= 5.4%+/- 15,平均体重指数(BMI)= 32.2 +/- 8 kg / m(2)。在单变量分析中,只有瘦素,sVCAM-1和sICAM-1与OSA严重性指数(即AHI和/或去饱和度)显着相关。在多元线性回归分析中,该分析控制了BMI,性别,年龄和当前吸烟状况;脱饱和持续作为sVCAM-1和瘦素升高的重要独立预测因子。结论:我们没有发现OSA与激活的先天免疫标志物(IL-1B,6和8)之间的显着关联。然而,OSA的严重程度与血清sVCAM-1和瘦素水平独立相关。这些可能代表了OSA相关CVD的发病机制。

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