Leenen F H, Tanner J, McNally C F
University of Ottawa Heart Institute, Ottawa, Ontario, Canada.
J Hum Hypertens. 2000 May;14(5):321-5. doi: 10.1038/sj.jhh.1001004.
To assess the antihypertensive efficacy of the angiotensin-converting enzyme (ACE)-inhibitor, perindopril, in the elderly, patients >65 years of age with supine diastolic blood pressure (BP) > or =90 and < or =110 mm Hg at the end of a 4-week placebo washout period were treated with perindopril 4-8 mg/daily vs placebo using a multicentre, randomised, double-blind, parallel group design. Of the 191 patients entered, 183 completed 8 weeks of double-blind therapy. Average age was 72-73 years. Supine and standing BP at the end of the placebo run-in period were 173/96 vs 168/96 mm Hg. BPs were measured in the morning, 20-25 h after the previous day's dose (ie, at the end of the dosing interval). In the placebo group, supine and standing diastolic BP decreased by 3-4 mm Hg, and systolic BP by 6-7 mm Hg. In the perindopril-group, diastolic BP decreased by 6-7 mm Hg and systolic BP by 10-13 mm Hg (both P < 0.01 vs placebo). These data indicate a substantial placebo response of particularly systolic BP in older hypertensives and indicate the importance of a parallel placebo-group to assess the extent of the actual drug's effect. Perindopril caused additional decreases in diastolic BP by about 2 mm Hg, and in systolic BP by 4-5 mm Hg. The extent of this drug-effect may be less in older vs middle-aged hypertensives.
为评估血管紧张素转换酶(ACE)抑制剂培哚普利对老年人的降压疗效,采用多中心、随机、双盲、平行组设计,对年龄>65岁、在4周安慰剂洗脱期结束时仰卧位舒张压(BP)≥90且≤110 mmHg的患者,给予培哚普利4 - 8 mg/日或安慰剂治疗。在纳入的191例患者中,183例完成了8周的双盲治疗。平均年龄为72 - 73岁。安慰剂导入期结束时仰卧位和站立位血压分别为173/96 mmHg和168/96 mmHg。血压于早晨测量,在前一天给药后20 - 25小时(即给药间隔结束时)测量。在安慰剂组,仰卧位和站立位舒张压下降3 - 4 mmHg,收缩压下降6 - 7 mmHg。在培哚普利组,舒张压下降6 - 7 mmHg,收缩压下降10 - 13 mmHg(与安慰剂相比,P均<0.01)。这些数据表明老年高血压患者尤其是收缩压存在显著的安慰剂反应,并表明平行安慰剂组对于评估实际药物疗效程度的重要性。培哚普利使舒张压额外下降约2 mmHg,收缩压额外下降4 - 5 mmHg。与中年高血压患者相比,该药在老年患者中的疗效程度可能较低。