Objectives: Although the pathophysiology of syndrome X (angina pectori
s, positive ECG test findings and normal coronary arteriogram) is uncl
ear, it is generally accepted that intracellular metabolic changes res
ulting from abnormal constriction of prearteriolar vessels due to endo
thelium-dependent vasodilation abnormalities may play a role in the pa
thogenesis. We established the effect of long-term treatment with cila
zapril, an angiotensin-converting enzyme inhibitor, which prevents the
effect of angiotensin II in the tonic control of vascular resistance.
Methods: 18 patients (15 women and 3 men, mean age 43.2 +/- 4.6 years
) with syndrome X were included in this study. A randomized double-bli
nd crossover placebo-controlled trial was done. After a 1-week washout
period, patients received either cilazapril 2 x 2.5 mg or placebo for
3 weeks, followed by 3 weeks of the other therapy. At the end of two
periods, an exercise ECG test (modified Bruce protocol) was employed.
Results: The magnitude of ST segment depression was significantly decr
eased during treatment with cilazapril compared with placebo. On the o
ther hand, total exercise time and time to 1 mm ST segment depression
were significantly prolonged by cilazapril. However, rate pressure pro
ducts were not significantly different at peak exercise at or at 1 mm
of ST segment depression during both therapies. Conclusion: Cilazapril
exerted a beneficial therapeutic effect in cases with syndrome X. The
possible mechanism of this effect may be a modulation of coronary ton
e at the microcirculation level.