Ogilvie R I, Piafsky K M, Ruedy J
Clin Pharmacol Ther. 1978 Nov;24(5):525-30. doi: 10.1002/cpt1978245525.
The antihypertensive effect of spironolactone was studied in 20 patients with essential hypertension and normal stimulated peripheral renin activity (PRA). Single-blind 8-wk treatment periods of placebo, 100, 200, and 400 mg spironolactone were used in consecutive order. Average supine and erect blood pressures were lower than placebo values at the end of each treatment. A prominent orthostatic effect was observed. Changes in blood pressure were not related to changes in body weight, PRA, or blood urea nitrogen. A larger proportion (50%) of patients had a more normal erect diastolic pressure at the end of 400 mg/day than at the end of 100 mg/day (20%), but the response to 400 mg/day could not be predicted from the responses to lower doses. Larger doses of spironolactone were predictably associated with rises in serum potassium, PRA, and aldosterone excretion. Adverse effects were absent during therapy with 100 mg/day but were frequent during 200--400 mg/day. Although there are no apparent advantages in increasing spironolactone from 100 to 200 mg/day in this group of patients with normal renin hypertension, increasing the dose to 400 mg/day resulted in better blood pressure control with more frequent adverse effects.
在20例原发性高血压且刺激外周肾素活性(PRA)正常的患者中研究了螺内酯的降压作用。采用单盲法,依次进行为期8周的安慰剂、100、200和400mg螺内酯治疗。每次治疗结束时,平均仰卧位和直立位血压均低于安慰剂组的值。观察到明显的直立位效应。血压变化与体重、PRA或血尿素氮的变化无关。与100mg/天治疗结束时相比,400mg/天治疗结束时更大比例(50%)的患者直立位舒张压更接近正常水平(20%),但无法根据低剂量的反应预测对400mg/天的反应。可以预见,更大剂量的螺内酯会导致血清钾、PRA和醛固酮排泄增加。100mg/天治疗期间无不良反应,但200 - 400mg/天治疗期间不良反应频繁。虽然在这群肾素性高血压正常的患者中,将螺内酯剂量从100mg/天增加到200mg/天没有明显优势,但将剂量增加到400mg/天可更好地控制血压,不过不良反应更频繁。