TY - JOUR
T1 - Coronary endothelial dysfunction is associated with a reduction in coronary artery compliance and an increase in wall shear stress
AU - Takumi, Takuro
AU - Yang, Eric H.
AU - Mathew, Verghese
AU - Rihal, Charanjit S.
AU - Gulati, Rajiv
AU - Lerman, Lilach O.
AU - Lerman, Amir
N1 - Copyright:
Copyright 2011 Elsevier B.V., All rights reserved.
PY - 2010/5
Y1 - 2010/5
N2 - Objective: Endothelial dysfunction is associated with arterial stiffness in large arteries. The purpose of this study was to investigate the association between coronary endothelial dysfunction, coronary artery compliance and wall shear stress in patients with early atherosclerosis. Methods: Coronary endothelial function was assessed according to responses to intracoronary acetylcholine in 120 patients without significant coronary stenosis. Acceleration of peak velocity (ACC), which is inversely related to coronary artery compliance, was derived from coronary flow velocity spectra, and wall shear rate (WSR) was calculated. Measurements were performed at baseline and after intracoronary nitroglycerin in order to eliminate the contribution of vascular smooth muscle tone to coronary artery compliance. Results: In all patients, heart rate significantly increased (72±1 to 77±1 bpm, p<0.01) and mean arterial pressure decreased (97±2 to 93±1 mm Hg, p<0.01) after nitroglycerin. Coronary blood flow (CBF) and resistance were not significantly changed, but the diastolic to systolic velocity ratio increased significantly (2.15±0.08 to 5.36±0.61, p<0.01). Patients with abnormal endothelial function (n=70) had a higher WSR at baseline (559±41 vs 440±26 s-1, p<0.05) and after nitroglycerin (457±41 vs 339±29 s-1, p<0.05), and a higher ACC after nitroglycerin (3.9±0.4 vs 2.8±0.4 m/s 2, p<0.05) than patients with normal function (n=50). Conclusions: The current study demonstrates that intracoronary nitroglycerin does not contribute to an increase of CBF but alters the phasic coronary flow pattern. Furthermore, early coronary atherosclerosis characterised by endothelial dysfunction is associated with a decrease in coronary artery compliance and an increase in wall shear stress. Therefore, coronary wall properties are affected early in the atherosclerosis process.
AB - Objective: Endothelial dysfunction is associated with arterial stiffness in large arteries. The purpose of this study was to investigate the association between coronary endothelial dysfunction, coronary artery compliance and wall shear stress in patients with early atherosclerosis. Methods: Coronary endothelial function was assessed according to responses to intracoronary acetylcholine in 120 patients without significant coronary stenosis. Acceleration of peak velocity (ACC), which is inversely related to coronary artery compliance, was derived from coronary flow velocity spectra, and wall shear rate (WSR) was calculated. Measurements were performed at baseline and after intracoronary nitroglycerin in order to eliminate the contribution of vascular smooth muscle tone to coronary artery compliance. Results: In all patients, heart rate significantly increased (72±1 to 77±1 bpm, p<0.01) and mean arterial pressure decreased (97±2 to 93±1 mm Hg, p<0.01) after nitroglycerin. Coronary blood flow (CBF) and resistance were not significantly changed, but the diastolic to systolic velocity ratio increased significantly (2.15±0.08 to 5.36±0.61, p<0.01). Patients with abnormal endothelial function (n=70) had a higher WSR at baseline (559±41 vs 440±26 s-1, p<0.05) and after nitroglycerin (457±41 vs 339±29 s-1, p<0.05), and a higher ACC after nitroglycerin (3.9±0.4 vs 2.8±0.4 m/s 2, p<0.05) than patients with normal function (n=50). Conclusions: The current study demonstrates that intracoronary nitroglycerin does not contribute to an increase of CBF but alters the phasic coronary flow pattern. Furthermore, early coronary atherosclerosis characterised by endothelial dysfunction is associated with a decrease in coronary artery compliance and an increase in wall shear stress. Therefore, coronary wall properties are affected early in the atherosclerosis process.
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U2 - 10.1136/hrt.2009.187898
DO - 10.1136/hrt.2009.187898
M3 - Article
C2 - 20448128
AN - SCOPUS:77952592133
SN - 1355-6037
VL - 96
SP - 773
EP - 778
JO - Heart
JF - Heart
IS - 10
ER -