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原发性醛固酮增多症患者中醛固酮合酶抑制与盐皮质激素受体阻断的序贯比较。

Sequential comparison of aldosterone synthase inhibition and mineralocorticoid blockade in patients with primary aldosteronism.

机构信息

Université Paris Descartes, Faculté de Médecine, Paris, France.

出版信息

J Hypertens. 2013 Mar;31(3):624-9; discussion 629. doi: 10.1097/HJH.0b013e32835d6d49.

Abstract

OBJECTIVE

We compared the effects of aldosterone synthase inhibition with LCI699 with those of mineralocorticoid receptor blockade in patients with primary aldosteronism.

METHODS

After a 2-week placebo run-in, 14 patients with primary aldosteronism received oral LCI699 (0.5 mg b.i.d.) from day 1 to 14, LCI699 (1 mg b.i.d.) from day 15 to 29, and placebo from day 29 to 36. From day 36 to day 66, patients were treated with eplerenone (50 mg b.i.d., up-titrated to 100 mg b.i.d. in 12/14 patients), in addition to their previous antihypertensive treatment, which was maintained unchanged.

RESULTS

Eplerenone significantly decreased more 24-h ambulatory SBP on day 66 than LCI699 on day 29 and the difference between the two treatment was -5.34 [95% confidence interval (CI) -10.30; -0.38)] mmHg (P = 0.027). Plasma potassium concentration achieved on eplerenone (4.30 ± 0.45 mmol/l) was significantly greater than on LCI699 (3.89 ± 0.35 mmol/l; P = 0.009). The increase in plasma renin concentration was significantly greater after eplerenone [+131% (range 61; 231)] than on LCI699 on day 29 [+39% (range 5; 86); P = 0.023]. LCI699 markedly decreased plasma aldosterone concentration by 75% (range -84;-63), whereas eplerenone markedly increased this concentration, from day 36, by 89% (range 40;154; P < 0.0001 vs. day 29).

CONCLUSION

In patients with primary aldosteronism, the effects on blood pressure and plasma potassium and renin concentrations of 4 weeks of eplerenone treatment (50-100 mg b.i.d.) were more marked than those of 4 weeks of LCI699 treatment (0.5-1 mg b.i.d.). These two drugs had opposite effects on plasma aldosterone concentration.

摘要

目的

我们比较了醛固酮合酶抑制剂 LCI699 与盐皮质激素受体阻断剂在原发性醛固酮增多症患者中的疗效。

方法

在为期 2 周的安慰剂导入期后,14 名原发性醛固酮增多症患者从第 1 天到第 14 天接受 LCI699(0.5mg 每日两次)治疗,从第 15 天到第 29 天接受 LCI699(1mg 每日两次)治疗,从第 29 天到第 36 天接受安慰剂治疗。从第 36 天到第 66 天,患者在接受之前的降压治疗的基础上,加用依普利酮(50mg 每日两次,14 名患者中的 12 名逐渐增至 100mg 每日两次)治疗,且其降压治疗不变。

结果

与第 29 天的 LCI699 相比,第 66 天依普利酮显著降低了更多的 24 小时动态收缩压(-5.34mmHg,95%置信区间[CI]为-10.30 至-0.38)(P=0.027)。依普利酮(4.30±0.45mmol/L)使血浆钾浓度显著升高,高于 LCI699(3.89±0.35mmol/L;P=0.009)。依普利酮治疗第 29 天时,血浆肾素浓度的升高幅度明显大于 LCI699(+131%[范围为 61%;231%])(P=0.023)。LCI699 可使血浆醛固酮浓度显著降低 75%(范围为-84%至-63%),而依普利酮可使血浆醛固酮浓度从第 36 天开始显著升高 89%(范围为 40%至 154%;P<0.0001 与第 29 天相比)。

结论

在原发性醛固酮增多症患者中,4 周依普利酮治疗(50-100mg 每日两次)对血压、血浆钾和肾素浓度的影响比 4 周 LCI699 治疗(0.5-1mg 每日两次)更为显著。这两种药物对血浆醛固酮浓度有相反的影响。

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