Park Jeong Bae, Ha Jong-Won, Jung Hae-Ok, Rhee Moo-Yong
aDivision of Cardiology/Medicine, Cheil General Hospital, Kwandong University College of Medicine bDivision of Cardiology, Severance Hospital, Yonsei University College of Medicine cDivision of Cardiology, The Catholic University of Korea, Seoul St Mary's Hospital, Seoul dCardiovascular Center, Dongguk University Ilsan Hospital, Goyang-si, Gyeonggi-do, Korea.
Blood Press Monit. 2014 Oct;19(5):294-301. doi: 10.1097/MBP.0000000000000061.
Measurement of central blood pressure provides prognostic information beyond conventional peripheral blood pressure (BP). However, few studies have directly compared the effects of antihypertensives on central hemodynamics. This study investigated the effects of a low-dose combination of nifedipine Gastrointestinal Therapeutic System (GITS) and valsartan versus high-dose monotherapy with either agent in reducing central BP in essential hypertension inadequately controlled by low-dose monotherapy.
In this prospective, open-label, randomized, active-controlled, multicenter 8-week study, patients not meeting the target BP after 4 weeks of treatment with low-dose monotherapy were randomized to receive nifedipine GITS 30 mg plus valsartan 80 mg (N30+V80), nifedipine GITS 60 mg (N60), or valsartan 160 mg (V160) for a further 4 weeks. Central hemodynamics were measured by applanation tonometry.
A total of 391 patients were enrolled. Reduction in central systolic BP from baseline to week 8, the primary efficacy variable, was significantly greater in the N30+V80 group (-27.2±14.7 mmHg) and the N60 group (-27.1±16.5 mmHg) compared with V160 group (-14.4±16.6 mmHg). Decrease in the augmentation index in the N60 group was significantly greater compared with V160 alone, without differences between combination therapy and either high-dose monotherapy. Decreases in brachial systolic BP were significantly greater in the N30+V80 and N60 groups than in the V160 group. By multiple regression analysis, most differences in drug effects on central hemodynamics disappeared after controlling for changes in peripheral BP. A low rate of adverse events occurred in all treatment groups.
A low-dose combination of nifedipine GITS plus valsartan or high-dose nifedipine was more effective in improving central hemodynamics than high-dose valsartan in patients with hypertension, mostly because of the improvement in peripheral (brachial) hemodynamics.
测量中心血压可提供超越传统外周血压(BP)的预后信息。然而,很少有研究直接比较抗高血压药物对中心血流动力学的影响。本研究调查了硝苯地平胃肠道治疗系统(GITS)与缬沙坦低剂量联合用药与高剂量单药治疗对原发性高血压患者中心血压的影响,这些患者在低剂量单药治疗下血压控制不佳。
在这项前瞻性、开放标签、随机、活性对照、多中心8周研究中,低剂量单药治疗4周后未达到目标血压的患者被随机分组,接受硝苯地平GITS 30mg加缬沙坦80mg(N30+V80)、硝苯地平GITS 60mg(N60)或缬沙坦160mg(V160),再治疗4周。通过压平式眼压测量法测量中心血流动力学。
共纳入391例患者。从基线到第8周中心收缩压的降低作为主要疗效变量,N30+V80组(-27.2±14.7mmHg)和N60组(-27.1±16.5mmHg)显著大于V160组(-14.4±16.6mmHg)。N60组的增强指数降低显著大于单独使用V160组,联合治疗与高剂量单药治疗之间无差异。N30+V80组和N60组肱动脉收缩压的降低显著大于V160组。通过多元回归分析,在控制外周血压变化后,药物对中心血流动力学影响的大多数差异消失。所有治疗组不良事件发生率较低。
硝苯地平GITS加缬沙坦低剂量联合用药或高剂量硝苯地平在改善高血压患者中心血流动力学方面比高剂量缬沙坦更有效,主要是因为外周(肱动脉)血流动力学得到改善。