Nh. Buus et al., Reduced vasodilator capacity in syndrome X related to structure and function of resistance arteries, AM J CARD, 83(2), 1999, pp. 149-154
Citations number
28
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
The combination of angina pectoris, angiographically normal epicardial coro
nary arteries, and a positive exercise test is referred to as syndrome X. P
revious studies have demonstrated an impaired coronary flow reserve and a p
eripheral vascular dysfunction, suggesting that vascular abnormalities in s
yndrome X may not be confined to the heart. The aim of this study was to in
vestigate whether any vascular disorder of syndrome X is due to intrinsic s
tructural or functional disturbances in resistance arteries. We compared 16
patients with syndrome X (56.6 +/- 1.2 years, 3 men) with 15 matched contr
ol subjects. Myocardial blood flow was measured with N-13-ammonia positron
emission tomography. Forearm blood flow was measured in the brachial artery
with high-resolution ultrasound. Gluteal subcutaneous resistance arteries
were dissected and mounted on a myograph for measurement of active tension
development, lumen diameter, and media thickness. Baseline myocardial blood
flow was similar in patients and controls, but dipyridamole-induced hypere
mia was decreased in patients (1.67 +/- 0.13 vs 2.31 +/- 0.12 ml/min/g, p <
0.01). Patients and controls had similar baseline forearm blood flow, but h
yperemic flow after transient occlusion of the brachial artery was impaired
in patients (198 +/- 20 vs 273 +/- 32 ml/min, p < 0.05). isolated resistan
ce arteries showed no differences in constriction to noradrenaline, or rela
xation to acetylcholine, dipyridamole, or nitroglycerin. Furthermore, the r
atio between media thickness and lumen diameter were similar in syndrome X
patients and controls. Our data show that when compared with a well-matched
control group, syndrome X patients have a decreased coronary and periphera
l vasodilator capacity. However, this is not reflected by functional abnorm
alities or structural changes as evaluated in subcutaneous resistance arter
ies. We conclude that syndrome X is not a generalized intrinsic abnormality
of the resistance circulation. (C) 1999 by Excerpta Medico, Inc.