Sleep Disorders Center, Department of Thoracic Medicine, University of Crete, Heraklion, Greece.
Mediators Inflamm. 2017;2017:4573756. doi: 10.1155/2017/4573756. Epub 2017 Jul 31.
Systemic inflammation is important in obstructive sleep apnea (OSA) pathophysiology and its comorbidity. We aimed to assess the levels of inflammatory biomarkers in a large sample of OSA patients and to investigate any correlation between these biomarkers with clinical and polysomnographic (PSG) parameters. This was a cross-sectional study in which 2983 patients who had undergone a polysomnography for OSA diagnosis were recruited. Patients with known comorbidities were excluded. Included patients ( = 1053) were grouped according to apnea-hypopnea index (AHI) as mild, moderate, and severe. Patients with AHI < 5 served as controls. Demographics, PSG data, and levels of high-sensitivity C-reactive protein (hs-CRP), fibrinogen, erythrocyte sedimentation rate (ESR), and uric acid (UA) were measured and compared between groups. A significant difference was found between groups in hs-CRP, fibrinogen, and UA. All biomarkers were independently associated with OSA severity and gender ( < 0.05). Females had increased levels of hs-CRP, fibrinogen, and ESR ( < 0.001) compared to men. In contrast, UA levels were higher in men ( < 0.001). Our results suggest that inflammatory markers significantly increase in patients with OSA without known comorbidities and correlate with OSA severity. These findings may have important implications regarding OSA diagnosis, monitoring, treatment, and prognosis. This trial is registered with ClinicalTrials.gov number NCT03070769.
系统性炎症在阻塞性睡眠呼吸暂停(OSA)病理生理学及其合并症中很重要。我们旨在评估大量 OSA 患者的炎症生物标志物水平,并研究这些生物标志物与临床和多导睡眠图(PSG)参数之间的任何相关性。这是一项横断面研究,共招募了 2983 名接受 OSA 诊断多导睡眠图检查的患者。排除已知合并症的患者。纳入的患者(n=1053)根据呼吸暂停低通气指数(AHI)分为轻度、中度和重度。AHI<5 的患者作为对照组。测量并比较了各组之间的人口统计学、PSG 数据以及高敏 C 反应蛋白(hs-CRP)、纤维蛋白原、红细胞沉降率(ESR)和尿酸(UA)的水平。hs-CRP、纤维蛋白原和 UA 在各组之间存在显著差异。所有生物标志物均与 OSA 严重程度和性别独立相关(<0.05)。与男性相比,女性的 hs-CRP、纤维蛋白原和 ESR 水平升高(<0.001)。相比之下,男性的 UA 水平较高(<0.001)。我们的研究结果表明,在无已知合并症的 OSA 患者中,炎症标志物显著增加,并与 OSA 严重程度相关。这些发现可能对 OSA 的诊断、监测、治疗和预后具有重要意义。该试验在 ClinicalTrials.gov 注册号为 NCT03070769 处注册。