The Fixed-Dose Combination of Olmesartan/Amlodipine Was Superior in Central Aortic Blood Pressure Reduction Compared with Perindopril/Amlodipine: A Randomized, Double-Blind Trial in Patients with Hypertension

被引:24
作者
Ruilope, Luis [1 ,2 ]
Schaefer, Angie [3 ]
机构
[1] Hosp 12 Octubre, Hypertens Unit, E-28041 Madrid, Spain
[2] Univ Autonoma Madrid, Dept Prevent Med & Publ Hlth, Madrid, Spain
[3] Dauchi Sankyo Europe GmbH, D-81379 Munich, Germany
关键词
Angiotensin-converting enzyme inhibitor; Angiotensin II receptor antagonist; Calcium channel blocker; Cardiology; Central systolic blood pressure; Fixed-dose combination; Non-invasive CV analysis system; Uncontrolled hypertension; OLMESARTAN MEDOXOMIL; CARDIOVASCULAR EVENTS; AMLODIPINE; MANAGEMENT; EFFICACY; MODERATE; OUTCOMES;
D O I
10.1007/s12325-013-0076-6
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Central blood pressure (BP), an important measure of cardiovascular risk, has been shown to be effectively reduced by calcium channel blockade with amlodipine (AML) plus renin-angiotensin system blockade by the angiotensin-converting enzyme inhibitor, perindopril (PER). The aim of the SEVITENSION study was to compare the central effects of PER/AML against renin-angiotensin system blockade with the angiotensin II receptor blocker olmesartan (OLM) plus AML. In this multicenter, parallel group, non-inferiority study, patients received AML 10 mg during a 2- to 4-week run-in before randomization to 24 weeks of double-blind treatment with the fixed-dose combination of OLM/AML 40/10 mg or PER/AML 8/10 mg. Hydrochlorothiazide was added at Weeks 4, 8, or 12 in patients with inadequate BP control. The primary efficacy variable was the absolute change in central systolic BP (CSBP) from baseline to the final examination, measured by radial artery applanation tonometry and analyzed by parametric analysis of covariance. Secondary variables included 24-h ambulatory and seated BP measurements as well as BP normalization. Of 600 patients enrolled, 486 were randomized (244 to OLM/AML 40/10 mg, 242 to PER/AML 8/10 mg). The reduction in CSBP was larger with OLM/AML (14.5 +/- A 0.83 mmHg) than with PER/AML (10.4 +/- A 0.84 mmHg). The between-group difference was -4.2 +/- A 1.18 mmHg with 95% confidence intervals (-6.48 to -1.83 mmHg) within the predefined non-inferiority margin (2 mmHg). An integrated superiority test confirmed that OLM/AML was superior to PER/AML (p < 0.0001) in reducing CSBP. The superiority of OLM/AML over PER/AML was also established for the majority of secondary efficacy variables; at the final examination, 75.6% of OLM/AML recipients achieved BP normalization (mean seated systolic BP/diastolic BP < 140/90 mmHg) compared with 57.5% of PER/AML recipients (p < 0.0001). The combination of OLM/AML was superior to PER/AML in reducing CSBP and other efficacy measures, including a significantly higher rate of BP normalization.
引用
收藏
页码:1086 / 1099
页数:14
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