C. Cardillo et al., EFFECTS OF BENAZEPRIL ON STRESS-TESTING BLOOD-PRESSURE IN ESSENTIAL-HYPERTENSION, The American journal of cardiology, 73(5), 1994, pp. 368-373
The effects of different doses of the angiotensin converting enzyme in
hibitor benazepril on cardiovascular response to a set of standardized
laboratory tasks were analyzed. Eighteen patients (15 men and 3 women
) with mild-to-moderate essential hypertension were randomly allocated
to receive 10 or 20 mg of benazepril, or placebo, each administered o
nce daily for 2 weeks, according to a double-blind, 3-period design. A
t the end of each treatment period, patients were examined at resting
baseline and while performing mental arithmetic, handgrip and cycle er
gometry tests. In comparison with placebo, the average reductions in r
esting systolic blood pressure (BP) were 8.7 mm Hg (95% confidence int
ervals [CI] -15.2 to -2.1) with 10 mg of benazepril, and 7.8 mm Hg (95
% CI -14.4 to -1.3) with 20 mg; the corresponding reductions in restin
g diastolic BP were 5.1 mm Hg (95% CI -8.7 to -1.4) and 6.8 mm Hg (95%
CI -10.4 to -3.1) (all p < 0.05). During mental arithmetic, the reduc
tions in systolic BP were 10.4 mm Hg (95% CI -17.4 to -3.4) with 10 mg
of benazepril, and 13.8 mm ng (95% CI -20.8 to -6.8) with 20 md diast
olic BP was reduced by 4.5 mm Hg (95% CI -8.5 to -0.5) and 8.3 mm ng (
95% CI -13.2 to -4.3), respectively (all p < 0.05). During the handgri
p test, systolic and diastolic BP were significantly reduced after 20
mg of benazepril by 10.8 mm Hg (95% CI -20.6 to -1) and as mm Hg (95%
CI -12.7 to -1.1), respectively (both p < 0.05); the reductions in sys
tolic and diastolic BP observed after 10 mg of benazepril did not achi
eve statistical significance (9.2 mm Hg [95% CI -19.1 to 0.6] and 2.1
mm Hg [95% CI -7.9 to 3.7], respectively; both p > 0.05). During ergom
etry, no active treatment significantly affected systolic and diastoli
c BP values (all p > 0.05). During mental arithmetic and the handgrip
test, there was no treatment effect on the magnitude of BP reactivity
from baseline (all p > 0.05); during ergometry, systolic BP reactivity
was higher after both benazepril doses than after placebo (both p < 0
.05). The data suggest that benazepril, especially at higher doses, ma
y be effective in reducing BP not only at rest, but also during some c
ommonly recurring stressful situations.