Reversal of peripheral microvascular dysfunction during long-term treatment with the angiotensin-converting enzyme inhibitor fosinopril in congestiveheart failure
S. Galatius et al., Reversal of peripheral microvascular dysfunction during long-term treatment with the angiotensin-converting enzyme inhibitor fosinopril in congestiveheart failure, J CARD FAIL, 5(1), 1999, pp. 17-24
Background: Treatment with angiotensin-converting enzyme (ACE) inhibitors i
n congestive heart failure (CHF) improves cardiac and peripheral hemodynami
c function and exercise performance. However, studies on the effects of lon
g-term treatment with an ACE inhibitor on the neurogenic and nonneurogenic
regulation and structural microangiopathy of the peripheral microvasculatur
e in CHF are lacking.
Methods and Results: We investigated the effect of 12 weeks of treatment wi
th the ACE inhibitor fosinopril on peripheral microvascular function in a d
ouble-blind, placebo-controlled study of 12 patients treated with fosinopri
l and 10 patients treated with placebo. All had moderate CHF, Microvascular
blood flow and resistance were calculated after application of the local i
sotope washout method in relaxed and nonrelaxed calf vascular beds in the s
upine position and during head-up tilt. Skeletal muscle vascular resistance
was reduced in the fosinopril group (46 +/- 6 to 30 +/- 1 mm Hg.mL(-1) 100
g.min +/- standard error; P < .05) and differed compared with the effect o
f placebo (P < .05) where no change was seen (37 +/- 11 to 55 +/- 13 mm Hg.
mL(-1) 100 g.min; not significant [NS]). Also, skin minimal vascular resist
ance was reduced during fosinopril treatment (13 +/- 0.6 to 11 +/- 0.7 mm H
g-mL(-1).100 g, min; P < .05) and differed compared with the effect of plac
ebo (P < .05) with absence of change (12 +/- 1.6 to 14 +/- 1.4 mm Hg.mL(-1)
100 g min; NS).
Conclusions: These results suggest that long-term ACE inhibitor treatment w
ith fosinopril in patients with CHF improves hemodynamic status to as far a
s the peripheral microvascular level in both the relaxed and nonrelaxed mic
rocirculation of the lower leg.