Petersen J R, Drabaek H, Gleerup G, Mehlsen J, Petersen L J, Winther K
Department of Clinical Physiology, Frederiksberg Hospital, Frederiksberg, Denmark.
Angiology. 1996 Mar;47(3):233-40. doi: 10.1177/000331979604700303.
The effects of the ACE inhibitor spirapril and of hydrochlorothiazide on left ventricular diastolic function were studied. Thirteen patients with mild to moderate essential hypertension completed this randomized, double-blinded, placebo-controlled, crossover study. After a three-week run-in period the patients entered three periods lasting four weeks each, wherein they were treated with placebo, spirapril, or hydrochlorothiazide. Blood pressure, hemodynamic variables (stroke volume, heart rate, cardiac output, index of contractility, and systemic vascular resistance), echocardiography (left ventricular mass), and Doppler-derived atrial to early (A/E)-ratio velocity time integrals (VTI) were measured at the end of each of the four periods. Spirapril lowered the A/E-ratio VTIs (0.57, 0.12-1.00) (P < 0.02) as compared with both placebo (0.80, 0.50-2.67) and hydrochlorothiazide (0.83, 0.44-1.25), and the drug normalized the A/E-ratio VTI in those patients with elevated values. The hemodynamic variables, left ventricular mass, and end-systolic wall stress were unchanged during all three treatments. There were no significant changes in mean blood pressure during the treatment periods. These results indicate that spirapril lowers A/E ratio within four weeks in patients with mild to moderate essential hypertension. It thereby seems able to improve left ventricular diastolic function. The effect is not dependent upon changes in hemodynamic variables, blood pressure, left ventricular mass, or end-systolic wall stress.
研究了血管紧张素转换酶(ACE)抑制剂螺普利和氢氯噻嗪对左心室舒张功能的影响。13例轻至中度原发性高血压患者完成了这项随机、双盲、安慰剂对照的交叉研究。经过为期3周的导入期后,患者进入3个为期4周的阶段,分别接受安慰剂、螺普利或氢氯噻嗪治疗。在每个4周阶段结束时,测量血压、血流动力学变量(每搏输出量、心率、心输出量、收缩性指数和全身血管阻力)、超声心动图(左心室质量)以及多普勒衍生的心房与早期(A/E)比值速度时间积分(VTI)。与安慰剂(0.80,0.50 - 2.67)和氢氯噻嗪(0.83,0.44 - 1.25)相比,螺普利降低了A/E比值VTI(0.57,0.12 - 1.00)(P < 0.02),并且该药物使A/E比值VTI在那些值升高的患者中恢复正常。在所有三种治疗期间,血流动力学变量、左心室质量和收缩末期壁应力均未改变。治疗期间平均血压无显著变化。这些结果表明,螺普利在4周内可降低轻至中度原发性高血压患者的A/E比值。因此,它似乎能够改善左心室舒张功能。该作用不依赖于血流动力学变量、血压、左心室质量或收缩末期壁应力的变化。