Hasdai D, Gibbons R J, Holmes D R, Higano S T, Lerman A
Division of Internal Medicine and Cardiovascular Diseases, Mayo Clinic and Foundation, Rochester, Minn 55905, USA.
Circulation. 1997 Nov 18;96(10):3390-5. doi: 10.1161/01.cir.96.10.3390.
Coronary endothelial dysfunction may occur in patients with minimally obstructive coronary artery disease and angina, and potentially may cause myocardial ischemia.
Coronary endothelium-dependent vasodilation was examined in patients with angina and <50% coronary artery diameter (CAD) stenosis by selectively infusing acetylcholine (10(-6) mol/L to 10(-4) mol/L) into the left anterior descending coronary artery (LAD). Percent change in CAD (%deltaCAD) was measured by quantitative coronary angiography, and percent change in coronary blood flow (%deltaCBF) was calculated using intracoronary flow Doppler. Coronary endothelium-independent vasodilation was examined using intracoronary adenosine and nitroglycerin. 99mTc sestamibi was injected intravenously just prior to the infusion of the highest dose of acetylcholine. Patients were divided blindly into three groups: Perfusion defects in non-LAD territory (group 1, n=6), no perfusion defects (group 2, n=7), and perfusion defects in the LAD territory (group 3, n=7). All patients had intact endothelium-independent vasodilation. In group 1, perfusion defects outside the LAD territory reflected an increase in %deltaCAD and %deltaCBF by 24+/-5% and 241+/-46% in the LAD. In group 2, %deltaCAD decreased by 26+/-5%, but %deltaCBF increased by 54+/-17%. In group 3, perfusion defects were within the LAD territory, reflecting a decrease in %deltaCAD and %deltaCBF by 35+/-5% and 51+/-14%, respectively.
This study demonstrates that coronary endothelial dysfunction in humans may be temporally associated with myocardial perfusion defects and supports a role for the coronary epicardial and microcirculation endothelium in regulating myocardial perfusion. Myocardial ischemia may occur in humans with impaired endothelium-dependent coronary flow reserve of the coronary epicardial and microcirculation.
冠状动脉内皮功能障碍可能发生在冠状动脉疾病阻塞程度较轻且有心绞痛症状的患者中,并可能导致心肌缺血。
通过向左前降支冠状动脉(LAD)选择性注入乙酰胆碱(10⁻⁶摩尔/升至10⁻⁴摩尔/升),对有心绞痛且冠状动脉直径(CAD)狭窄<50%的患者进行冠状动脉内皮依赖性血管舒张功能检测。通过定量冠状动脉造影测量CAD的百分比变化(%ΔCAD),并使用冠状动脉内血流多普勒计算冠状动脉血流的百分比变化(%ΔCBF)。使用冠状动脉内腺苷和硝酸甘油检测冠状动脉非内皮依赖性血管舒张功能。在注入最高剂量乙酰胆碱之前,静脉注射⁹⁹ᵐTc甲氧基异丁基异腈。患者被随机分为三组:非LAD区域灌注缺损(第1组,n = 6)、无灌注缺损(第2组,n = 7)和LAD区域灌注缺损(第3组,n = 7)。所有患者的非内皮依赖性血管舒张功能均正常。在第1组中,LAD区域外的灌注缺损反映LAD的%ΔCAD和%ΔCBF分别增加了24±5%和241±46%。在第2组中,%ΔCAD下降了26±5%,但%ΔCBF增加了54±17%。在第3组中,灌注缺损位于LAD区域内,分别反映%ΔCAD和%ΔCBF下降了35±5%和51±14%。
本研究表明,人类冠状动脉内皮功能障碍可能与心肌灌注缺损在时间上相关,并支持冠状动脉心外膜和微循环内皮在调节心肌灌注中的作用。冠状动脉心外膜和微循环的内皮依赖性冠状动脉血流储备受损的人类可能会发生心肌缺血。