Department of Respiratory and Sleep Medicine, Royal North Shore Hospital, St Leonards, New South Wales, Australia.
Thorax. 2012 Jul;67(7):639-44. doi: 10.1136/thoraxjnl-2011-200874. Epub 2012 Feb 14.
Obstructive sleep apnoea (OSA) is associated with increased cardiovascular risk, however the mechanisms are not well established.
This study aimed to determine whether treatment of OSA with nasal continuous positive airway pressure (CPAP) would favourably alter coagulability across the sleep-wake cycle.
In a randomised crossover trial, 28 patients received therapeutic or placebo CPAP, each for 2 months with a 1 month washout between treatments. After each treatment period, a 24 h coagulation study was conducted in the laboratory. Plasminogen activator inhibitor-1 (PAI-1), D-dimer, fibrinogen, von Willebrand Factor (vWF), factor VIII (FVIII), factor VII (FVII) and factor V (FV) were determined at seven time points over the day and night.
At baseline, patients had severe OSA (Apnoea Hypopnoea Index 37.9 ± 23.9 events/h). Treatment of OSA with CPAP compared with placebo resulted in lower 24 h levels of vWF (-3.9%, p=0.013), FVIII (-6.2%, p=0.007) and FV (-4.2%, p<0.001). The greatest difference occurred during the nocturnal and early morning periods. In contrast, fibrinogen, D-dimer, FVII and PAI-1 did not differ between treatments, however all markers displayed diurnal variability independent of treatment.
In this randomised, placebo-controlled crossover trial, treatment of OSA with CPAP reduced the early morning level of vWF, and nocturnal levels of FVIII and FV. These findings suggest that CPAP may reduce cardiovascular risk in OSA, in part through reducing risk of thrombosis.
阻塞性睡眠呼吸暂停(OSA)与心血管风险增加相关,但机制尚不清楚。
本研究旨在确定经鼻持续气道正压通气(CPAP)治疗 OSA 是否会在整个睡眠-觉醒周期中改变凝血功能。
在一项随机交叉试验中,28 名患者接受了治疗性或安慰剂 CPAP 治疗,每种治疗持续 2 个月,两种治疗之间有 1 个月的洗脱期。在每个治疗期后,在实验室中进行了 24 小时凝血研究。在白天和夜间的七个时间点测定纤溶酶原激活物抑制剂-1(PAI-1)、D-二聚体、纤维蛋白原、血管性血友病因子(vWF)、因子 VIII(FVIII)、因子 VII(FVII)和因子 V(FV)。
在基线时,患者患有严重的 OSA(呼吸暂停低通气指数 37.9±23.9 次/小时)。与安慰剂相比,CPAP 治疗 OSA 导致 vWF(-3.9%,p=0.013)、FVIII(-6.2%,p=0.007)和 FV(-4.2%,p<0.001)的 24 小时水平降低。最大的差异发生在夜间和清晨期间。相比之下,纤维蛋白原、D-二聚体、FVII 和 PAI-1在两种治疗之间没有差异,但所有标志物均表现出独立于治疗的昼夜变化。
在这项随机、安慰剂对照交叉试验中,CPAP 治疗 OSA 降低了清晨 vWF 水平和夜间 FVIII 和 FV 水平。这些发现表明,CPAP 可能通过降低血栓形成风险来降低 OSA 患者的心血管风险。