Fischler Manuel, Maggiorini Marco, Dorschner Lorenz, Debrunner Johann, Bernheim Alain, Kiencke Stephanie, Mairbäurl Heimo, Bloch Konrad E, Naeije Robert, Brunner-La Rocca Hans Peter
Intensive Care Unit, Department of Internal Medicine, University Hospital Zürich, Raemistrasse 100, CH-8091 Zürich, Switzerland.
Am J Respir Crit Care Med. 2009 Aug 15;180(4):346-52. doi: 10.1164/rccm.200808-1348OC. Epub 2009 Jun 11.
Whether pulmonary hypertension at high altitude limits exercise capacity remains uncertain.
To gain further insight into the pathophysiology of hypoxia induced pulmonary hypertension and the resulting reduction in exercise capacity, we investigated if the reduction in hypoxic pulmonary vasoconstrictive response with corticosteroids or phosphodiesterase-5 inhibition improves exercise capacity.
A cardiopulmonary exercise test and echocardiography to estimate systolic pulmonary artery pressure were performed in 23 subjects with previous history of high altitude pulmonary edema, known to be associated with enhanced hypoxic vasoconstriction. Subjects were randomized to dexamethasone 8 mg twice a day, tadalafil 10 mg twice a day, or placebo (double-blinded), starting the day before ascent.
Measurements were performed at low and high (i.e., 4,559 m) altitude. Altitude exposure decreased maximum oxygen uptake and oxygen saturation, increased pulmonary artery pressure, and altered oxygen uptake kinetics. Compared with placebo, dexamethasone improved maximum oxygen uptake (% predicted 74 +/- 13%; tadalafil 63 +/- 13%, placebo 61 +/- 11%; P < 0.05), oxygen kinetics (mean response time 41 +/- 13 s; tadalafil 46 +/- 6 s, placebo 45 +/- 10 s; P < 0.05), and reduced the ventilatory equivalent for CO(2) (42 +/- 4; tadalafil 49 +/- 4, placebo 50 +/- 5; P < 0.01). Peak oxygen saturation did not differ significantly between the three groups (dexamethasone 66 +/- 7%, placebo 62 +/- 7%, tadalafil 69 +/- 5%; P = 0.08). During echocardiography at low-intensity exercise (40% of peak power), dexamethasone compared with placebo resulted in lower pulmonary artery pressure (47 +/- 9 mm Hg; tadalafil 57 +/- 11 mm Hg, placebo 68 +/- 23 mm Hg; P = 0.05) and higher oxygen saturation (74 +/- 7%; tadalafil 67 +/- 3%, placebo 61 +/- 20; P < 0.02).
Corticosteroids, but not phosphodiesterase-5 inhibition, partially prevented the limitation of exercise capacity in subjects with intense hypoxic pulmonary vasoconstriction at high altitude.
高原地区的肺动脉高压是否会限制运动能力仍不明确。
为了进一步深入了解缺氧诱导的肺动脉高压的病理生理学以及由此导致的运动能力下降,我们研究了使用皮质类固醇或磷酸二酯酶-5抑制剂降低缺氧性肺血管收缩反应是否能提高运动能力。
对23名有高原肺水肿病史且已知与增强的缺氧性血管收缩有关的受试者进行了心肺运动试验和超声心动图检查以评估收缩期肺动脉压。受试者被随机分为每日两次服用8毫克地塞米松组、每日两次服用10毫克他达拉非组或安慰剂组(双盲),在登山前一天开始用药。
在低海拔和高海拔(即4559米)进行测量。暴露于高原环境会降低最大摄氧量和血氧饱和度,增加肺动脉压,并改变摄氧动力学。与安慰剂相比,地塞米松提高了最大摄氧量(预测值的74±13%;他达拉非为63±13%,安慰剂为61±11%;P<0.05)、改善了氧动力学(平均反应时间41±13秒;他达拉非为46±6秒,安慰剂为45±10秒;P<0.05),并降低了二氧化碳通气当量(42±4;他达拉非为49±4,安慰剂为50±5;P<0.01)。三组之间的峰值血氧饱和度无显著差异(地塞米松为66±7%,安慰剂为62±7%,他达拉非为69±5%;P = 0.08)。在低强度运动(峰值功率的40%)时进行超声心动图检查,与安慰剂相比,地塞米松导致肺动脉压更低(47±9毫米汞柱;他达拉非为57±11毫米汞柱,安慰剂为68±23毫米汞柱;P = 0.05),血氧饱和度更高(74±7%;他达拉非为67±3%,安慰剂为61±20;P<0.02)。
在高原地区,对于有强烈缺氧性肺血管收缩的受试者,皮质类固醇而非磷酸二酯酶-5抑制剂能部分预防运动能力受限。