Cohen J D, Drury J H, Ostdiek J, Finn J, Babu B R, Flaker G, Belew K, Donohue T, Labovitz A
Division of Cardiology, Department of Internal Medicine, Saint Louis University Health Sciences Center, MO 63104, USA.
Am Heart J. 2000 Apr;139(4):734-8. doi: 10.1016/s0002-8703(00)90057-7.
The favorable effects of lowering low-density lipoprotein (LDL)-cholesterol on reducing clinical events in patients with coronary disease have been well established. The mechanisms responsible for this benefit, however, have not been fully understood. This study examined the impact of lipid-lowering therapy on endothelium-dependent vasoreactivity in a subgroup of patients after myocardial infarction with average cholesterol levels who participated in the Cholesterol Recurrent Events (CARE) study to determine whether an effect on endothelial function is a viable mechanism for the observed reduction in clinical events.
Participants were recruited from among volunteers in the CARE trial at 2 university-based outpatient cardiology clinics. Patients were randomly assigned to pravastatin or placebo. Plasma lipids were measured at baseline and semiannually thereafter. During the final 6 months of the trial, vasoreactivity was assessed by change in ultrasound-determined brachial artery diameter in response to blood pressure cuff-induced ischemia (endothelium-dependent) and to nitroglycerin, a direct vasodilator. Differences in response were examined between the 2 randomized groups. The relation between change in LDL-cholesterol from baseline to year 5 and the magnitude of endothelium-dependent vasodilation also was examined. There was significantly greater endothelium-dependent vasodilation observed in the pravastatin group compared with the placebo group (13% vs 8%, P =.0002), with no difference between the groups in their response to the endothelium-independent vasodilator nitroglycerin. The magnitude of the endothelium-dependent vasodilation was significantly correlated with the percent change in LDL-cholesterol from baseline to final visit (r = 0.49, P =.015).
These findings indicate that the use of pravastatin in patients after myocardial infarction with average cholesterol levels is associated with greater endothelium-dependent vasodilation compared with those who received placebo. The magnitude of this vasodilatory response is correlated to the reduction in LDL-cholesterol. This improvement in endothelium-dependent vasoreactivity may be a likely mechanism, at least in part, for the reduction in recurrent clinical events observed and reported in the CARE study.
降低低密度脂蛋白(LDL)胆固醇对减少冠心病患者临床事件的有益作用已得到充分证实。然而,这种益处背后的机制尚未完全明确。本研究在参与胆固醇再发事件(CARE)研究的心肌梗死且胆固醇水平处于平均水平的患者亚组中,考察了降脂治疗对内皮依赖性血管反应性的影响,以确定对内皮功能的影响是否是观察到的临床事件减少的可行机制。
参与者从两所大学附属医院门诊心脏病诊所的CARE试验志愿者中招募。患者被随机分配至普伐他汀组或安慰剂组。在基线时及此后每半年测量血脂。在试验的最后6个月,通过超声测定肱动脉直径对血压袖带诱导的缺血(内皮依赖性)和直接血管扩张剂硝酸甘油的反应变化来评估血管反应性。检查两个随机分组之间的反应差异。还考察了从基线到第5年LDL胆固醇的变化与内皮依赖性血管舒张程度之间的关系。与安慰剂组相比,普伐他汀组观察到的内皮依赖性血管舒张明显更大(分别为13%对8%,P = 0.0002),两组对非内皮依赖性血管扩张剂硝酸甘油的反应无差异。内皮依赖性血管舒张的程度与从基线到最后一次访视时LDL胆固醇的百分比变化显著相关(r = 0.49,P = 0.015)。
这些发现表明,在心肌梗死后胆固醇水平处于平均水平的患者中,使用普伐他汀与接受安慰剂的患者相比,内皮依赖性血管舒张更大。这种血管舒张反应的程度与LDL胆固醇的降低相关。内皮依赖性血管反应性的这种改善可能至少部分是CARE研究中观察到并报道的复发性临床事件减少的可能机制。