Antihypertensive effect of the mineralocorticoid receptor antagonist eplerenone: a pooled analysis of patient-level data from comparative trials using regulatory-approved doses

被引:4
作者
Fernet, Mireille [1 ]
Beckerman, Bruce [2 ]
Abreu, Paula [2 ]
Lins, Katharina [3 ]
Vincent, John [2 ]
Burgess, Ellen [4 ]
机构
[1] Pfizer Canada Inc, Dept Med Affairs, Kirkland, PQ, Canada
[2] Pfizer Inc, Dept Clin Affairs, New York, NY USA
[3] Pfizer Ltd, Dept Med Affairs, Tadworth, England
[4] Univ Calgary, Dept Med, Fac Med, 1403-29th St NW, Calgary, AB T2N 2T9, Canada
关键词
hypertension; eplerenone; aldosterone; cardiovascular; selective mineralocorticoid blocker;
D O I
10.2147/VHRM.S170141
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Purpose: Several options are available for the treatment of hypertension; however, many treated patients are still not below blood pressure (BP) target. Eplerenone, a selective mineralocorticoid receptor antagonist, is an approved treatment option for the management of patients with hypertension in a number of countries. This patient-level pooled analysis was conducted to document the efficacy and safety/tolerability of eplerenone at the dosages approved for use in hypertension in comparison to placebo or other approved antihypertensive agents. Methods: Seventeen Phase III studies conducted in patients with mild-to-moderate hypertension in the Eplerenone Hypertension Clinical Program were reviewed; eleven met the selection criteria. The primary endpoint was change from baseline in seated diastolic BP and seated systolic BP measured at the end of the study. Results: A total of 2,698 patients were included in this per-protocol analysis. In patients treated for at least 6 weeks with a stable dose of eplerenone, doses of 50 mg daily and 100 mg daily were associated with greater reductions of seated systolic BP and seated diastolic BP compared with placebo (P<0.001) and active-controlled studies (P<0.033). In the analysis of covariance model testing of the contribution of four factors (age, body mass index [BMI], history of cardiovascular disease, and diabetes) on the BP lowering effects of eplerenone, only BMI and age were associated with small though statistically significant changes in BP (<0.2 mmHg). Eplerenone was well tolerated; headache was the most common adverse event for patients in any group. Severe hyperkalemia (serum potassium level >6.0 mmol/L) occurred in up to 0.4% in the eplerenone groups, 0.4% in the placebo group, and 0.1% in the active-control group. Conclusion: This patient-level pooled analysis provides robust evidence that eplerenone, at 50 mg or 100 mg daily, was effective in lowering BP in patients with mild-to-moderate hypertension and was well tolerated.
引用
收藏
页码:233 / 246
页数:14
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