Schulte K L, Meyer-Sabellek W, Liederwald K, van Gemmeren D, Lenz T, Gotzen R
Department of Medicine, Klinikum Steglitz, Free University, Berlin, Germany.
Am J Cardiol. 1992 Aug 15;70(4):468-73. doi: 10.1016/0002-9149(92)91192-7.
Casual as well as ambulatory 24-hour blood pressure (BP) and echocardiographic parameters were studied in 40 patients with untreated or insufficiently treated mild to moderate essential hypertension. Left ventricular (LV) hypertrophy was assessed before and after 24 weeks of therapy with either the converting enzyme inhibitor perindopril or the calcium antagonist nifedipine. The design was a double-blind parallel study with a placebo run-in period. Patients received a daily oral dosage of either 4 to 8 mg of perindopril or 40 to 80 mg of nifedipine in slow-release form. A diuretic (25 mg/day of hydrochlorothiazide) was added in nonresponders (greater than 90 mm Hg casual diastolic BP). Once-daily perindopril and twice-daily nifedipine comparably reduced both casual and ambulatory BP throughout 24 hours (p less than 0.01) without affecting 24-hour heart rate. Six subjects withdrew from the nifedipine group and 4 from the perindopril group. After 12 and 24 weeks of therapy, LV hypertrophy was significantly reduced by both agents. Before active treatment was begun, LV mass index was more closely correlated to 24-hour (p less than 0.001) than to casual BP. This correlation disappeared after treatment with both agents. The correlation between ambulatory systolic day-time BP and LV mass was only still present (r = 0.54; p less than 0.05) after 24 weeks of treatment with nifedipine. It is concluded that regression of LV hypertrophy during converting enzyme inhibition or calcium antagonism may be partly independent of dosage and magnitude of 24-hour BP decrease.
对40例未经治疗或治疗不充分的轻至中度原发性高血压患者进行了动态及非动态24小时血压和超声心动图参数研究。在使用转换酶抑制剂培哚普利或钙拮抗剂硝苯地平治疗24周前后评估左心室(LV)肥厚情况。设计为双盲平行研究,有安慰剂导入期。患者每日口服4至8毫克培哚普利或40至80毫克缓释硝苯地平。对无反应者(非动态舒张压大于90毫米汞柱)加用利尿剂(每日25毫克氢氯噻嗪)。每日一次的培哚普利和每日两次的硝苯地平在24小时内同等程度降低了动态及非动态血压(p小于0.01),且不影响24小时心率。硝苯地平组有6名受试者退出,培哚普利组有4名受试者退出。治疗12周和24周后,两种药物均使LV肥厚明显减轻。在开始积极治疗前,LV质量指数与24小时血压的相关性比与非动态血压的相关性更密切(p小于0.001)。两种药物治疗后这种相关性消失。硝苯地平治疗24周后,动态收缩期日间血压与LV质量之间仍存在相关性(r = 0.54;p小于0.05)。结论是,在转换酶抑制或钙拮抗治疗期间LV肥厚的消退可能部分独立于24小时血压降低的剂量和幅度。