Departments of Cardiology, Juntendo University School of Medicine.
Circ J. 2011;75(5):1071-9. doi: 10.1253/circj.cj-11-0141. Epub 2011 Apr 7.
A previous study reported that amlodipine retarded coronary plaque progression in patients with coronary artery disease. The goal of this multicenter study was to determine which calcium-channel blockers (CCBs) other than amlodipine attenuated the progression of plaque volume (PV) accessed by intravascular ultrasound (IVUS).
ALPS-J was a prospective, randomized open-label study conducted at 5 centers. Patients who had hypertension and were scheduled for coronary intervention were enrolled. Subjects were randomly assigned to receive 16 mg/day of azelnidipine or 5mg/day of amlodipine administered for 48 weeks. The primary endpoint was the percent change in coronary PV measured by IVUS. Between 2007 and 2009, 199 patients were enrolled; 115 had evaluable IVUS images at both baseline and after 48 weeks of treatment. Blood pressure significantly reduced to 128/68 mmHg at follow-up. The lipid profiles in the 2 groups were comparable (low-density lipoprotein cholesterol: 97 mg/dl). The %change in PV showed a significant regression of 4.67 and 4.85% in the azelnidipine and amlodipine groups, respectively. The upper limit of the 95% confidence interval of the mean difference in %change PV between the 2 groups (0.18%, 95% confidence interval 4.62 to 4.98%) did not exceed the pre-defined non-inferiority margin of 6.525%.
ALPS-J demonstrated that azelnidipine was not inferior to amlodipine for primary efficacy. In addition to standard medical therapy, dihydropyridine CCBs will retard PV progression in hypertensive patients.
先前的一项研究报告称,氨氯地平可延缓冠心病患者的冠状动脉斑块进展。本多中心研究的目的是确定除氨氯地平以外的哪些钙通道阻滞剂(CCB)可减轻血管内超声(IVUS)评估的斑块体积(PV)进展。
ALPS-J 是一项在 5 个中心进行的前瞻性、随机、开放标签研究。入选了患有高血压且计划进行冠状动脉介入治疗的患者。将受试者随机分为每日接受 16mg 阿折地平或 5mg 氨氯地平治疗 48 周。主要终点是 IVUS 测量的冠状动脉 PV 的百分比变化。2007 年至 2009 年期间,共入选 199 例患者;其中 115 例患者在基线和治疗 48 周后均有可评估的 IVUS 图像。随访时血压显著降低至 128/68mmHg。两组的血脂谱相似(低密度脂蛋白胆固醇:97mg/dl)。PV 的百分比变化显示阿折地平组和氨氯地平组分别有 4.67%和 4.85%的显著回归。两组间 %PV 变化的均值差异的 95%置信区间上限(0.18%,95%置信区间 4.62 至 4.98%)未超过预先设定的非劣效性界限 6.525%。
ALPS-J 表明阿折地平在主要疗效方面不劣于氨氯地平。除标准药物治疗外,二氢吡啶类 CCB 可延缓高血压患者的 PV 进展。