Effects of drospirenone/17-β estradiol on blood pressure and potassium balance in hypertensive postmenopausal women

被引:72
作者
Preston, RA
White, WB
Pitt, B
Bakris, G
Norris, PM
Hanes, V
机构
[1] Univ Miami, Sch Med, Clin Res Ctr, Div Clin Pharmacol & Pharmacokinet, Miami, FL USA
[2] Univ Miami, Sch Med, Dept Med, Miami, FL USA
[3] Univ Connecticut, Sch Med, Div Hypertens & Clin Pharmacol, Farmington, CT USA
[4] Univ Michigan, Sch Med, Ann Arbor, MI USA
[5] Rush Univ, Rush Med Coll, Chicago, IL 60612 USA
[6] Univ Miami, Sch Med, Dept Obstet & Gynecol, Div Gynecol, Miami, FL 33101 USA
[7] Berlex Labs Inc, Montville, NJ USA
关键词
hormone therapy; drospirenone; aldosterone; aldosterone antagonists; hyperkalemia; hypertension; progesterone; chronic renal failure;
D O I
10.1016/j.amjhyper.2004.12.003
中图分类号
R6 [外科学];
学科分类号
1002 [临床医学]; 100210 [外科学];
摘要
Background: Drospirenone (DRSP) is a novel progestin with aldosterone receptor antagonist activity developed for hormone therapy as DRSP /17-beta estradiol (DRSP/E2). Because of a significant aldosterone antagonist activity, we studied the effects of DRSP/E2 on serum potassium (K) and blood pressure (BP) in hypertensive postmenopausal women with and without diabetes mellitus. Methods: This was a multicenter trial in postmenopausal women 44 to 70 years of age, either with type 2 diabetes mellitus (n = 82) or without type 2 diabetes mellitus (n = 148) and using an angiotensin-converting enzyme (ACE) inhibitor or angiotensin II receptor antagonist. Patients were randomized to 28 days of DRSP/E2 or placebo. Study endpoints were the number and percentage subjects who developed hyperkalemia (K >= 5.5 mEq/L) and changes from baseline in clinic systolic and diastolic BP. To increase the likelihood of unmasking hyperkalemia, the nondiabetic group was also administered ibuprofen for 5 days. Results: There were no statistical differences in the overall number and percentage of subjects with hyperkalemia for DRSP/E2 versus placebo. No subject had symptoms or electrocardiographic changes related to hyperkalemia. Blood pressure was reduced by -8.6/-5.8 mm Hg in patients receiving DRSP/E2 versus -3.7/-2.9 mm Hg in those receiving placebo (P <.01 for both SBP and DBP). Conclusions: In hypertensive postmenopausal women, treatment with DRSP/E2 was not associated with a greater incidence of hyperkalemia than with placebo in patients with and without type 2 diabetes mellitus and concomitant use of ACE inhibitors, angiotensin receptor antagonists, or ibuprofen. Furthermore, DRSP/E2 was found to have a significant antihypertensive effect in this high-risk population.
引用
收藏
页码:797 / 804
页数:8
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