Naomi S, Umeda T, Iwaoka T, Sato T
Jpn Heart J. 1987 May;28(3):357-65. doi: 10.1536/ihj.28.357.
The validity of the captopril test for primary aldosteronism (PA) was tested in patients with surgically verified PA (n = 12) or essential hypertension (EHT, n = 20) with different levels of sodium intakes. The patients were scheduled on 7 days each of three regimes of the prepared diet containing 34, 120 and 340 mEq of sodium chloride per day, and the captopril test was repeated in each period. For the test, captopril (50 mg) was administered orally at 9:00 A.M. after 1 hour of rest in a supine position, and venous blood samples were obtained before and 90 min after drug administration. Plasma aldosterone concentration (PAC; ng/dl) and plasma renin activity (PRA; ng/ml/h) were measured by radioimmunoassay. Under the three different sodium intakes, a PAC/PRA ratio greater than 20 at 90 min after captopril administration was sufficiently sensitive (0.95, 19/20) and specific (0.92, 55/60) to identify PA. Similarly, PA was associated with a PAC above 15 ng/dl 90 min after captopril. There were no complaints associated with the antihypertensive effects of the drug even when patients were sodium-restricted. These results confirmed that the captopril test is safe and useful for screening out-patients for PA, independent of individual differences in sodium intake.
在不同钠摄入量水平下,对经手术证实为原发性醛固酮增多症(PA,n = 12)或原发性高血压(EHT,n = 20)的患者进行了卡托普利试验用于PA诊断的有效性测试。患者按照三种饮食方案安排,每种方案持续7天,分别含氯化钠34、120和340 mEq/天,且在每个阶段重复进行卡托普利试验。试验时,患者于上午9:00仰卧休息1小时后口服卡托普利(50 mg),并在给药前及给药后90分钟采集静脉血样。采用放射免疫分析法测定血浆醛固酮浓度(PAC;ng/dl)和血浆肾素活性(PRA;ng/ml/h)。在三种不同钠摄入量情况下,卡托普利给药后90分钟时PAC/PRA比值大于20对PA的诊断具有足够的敏感性(0.95,19/20)和特异性(0.92,55/60)。同样,卡托普利给药后90分钟时PA患者的PAC高于15 ng/dl。即使患者处于钠限制状态,也未出现与该药物降压作用相关的不适主诉。这些结果证实,卡托普利试验对于PA门诊患者筛查是安全且有用的,与钠摄入量的个体差异无关。