To assess the antihypertensive efficacy of the angiotensin-converting enzym
e (ACE)-inhibitor, perindopril, in the elderly, patients >65 years of age w
ith supine diastolic blood pressure (BP) greater than or equal to 90 and le
ss than or equal to 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-biind, parallel group design. Of the 191 patients enter
ed, 183 completed 8 weeks of double-blind therapy. Average age was 72-73 ye
ars. Supine and standing BP at the end of the placebo run-in period were 17
3/96 vs 168/96 mm Hg. BPs were measured in the morning, 20-25 h after the p
revious day's dose tie, at the end of the dosing interval). In the placebo
group, supine and standing diastolic BP decreased by 3-4 mmHg, and systolic
BP by 6-7 mm Hg. In the perindopril-group, diastolic BP decreased by 6-7 m
m 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 olde
r hypertensives and indicate the importance of a parallel placebo-group to
assess the extent of the actual drug's effect. Perindopril caused additiona
l 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 hype
rtensives.