Effect of spironolactone on blood pressure in subjects with resistant hypertension

被引:477
作者
Chapman, Neil
Dobson, Joanna
Wilson, Sarah
Dahlof, Bjorn
Sever, Peter S.
Wedel, Hans
Poulter, Neil R.
机构
[1] Imperial Coll Sch Med, Int Ctr Circulatory, London W2 1PG, England
[2] Sahlgrens Univ Hosp, S-41345 Gothenburg, Sweden
[3] Nord Sch Publ Hlth, Gothenburg, Sweden
关键词
blood pressure; hypertension; clinical trial; antihypertensive agents; aldosterone antagonists; spironolactone; PRIMARY HYPERALDOSTERONISM; PRIMARY ALDOSTERONISM; EFFICACY; PREVALENCE; THERAPY; AGENTS; RATES; RATIO;
D O I
10.1161/01.HYP.0000259805.18468.8c
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Spironolactone is recommended as fourth-line therapy for essential hypertension despite few supporting data for this indication. We evaluated the effect among 1411 participants in the Anglo-Scandinavian Cardiac Outcomes Trial-Blood Pressure Lowering Arm who received spironolactone mainly as a fourth-line antihypertensive agent for uncontrolled blood pressure and who had valid BP measurements before and during spironolactone treatment. Among those who received spironolactone, the mean age was 63 years (SD: +/- 8 years), 77% were men, and 40% had diabetes. Spironolactone was initiated a median of 3.2 years (interquartile range: 2.0 to 4.4 years) after randomization and added to a mean of 2.9 (SD: +/- 0.9) other antihypertensive drugs. The median duration of spironolactone treatment was 1.3 years (interquartile range: 0.6 to 2.6 years). The median dose of spironolactone was 25 mg (interquartile range: 25 to 50 mg) at both the start and end of the observation period. During spironolactone therapy, mean blood pressure fell from 156.9/85.3 mm Hg (SD: +/- 18.0/11.5 mm Hg) by 21.9/9.5 mm Hg (95% CI: 20.8 to 23.0/9.0 to 10.1 mm Hg; P < 0.001); the BP reduction was largely unaffected by age, sex, smoking, and diabetic status. Spironolactone was generally well tolerated; 6% of participants discontinued the drug because of adverse effects. The most frequent adverse events were gynecomastia or breast discomfort and biochemical abnormalities (principally hyperkaliemia), which were recorded as adverse events in 6% and 2% of participants, respectively. In conclusion, spironolactone effectively lowers blood pressure in patients with hypertension uncontrolled by a mean of approximate to 3 other drugs. Although nonrandomized and not placebo controlled, these data support the use of spironolactone in uncontrolled hypertension.
引用
收藏
页码:839 / 845
页数:7
相关论文
共 32 条
[1]   COMPARISON OF SURGERY AND PROLONGED SPIRONOLACTONE THERAPY IN PATIENTS WITH HYPERTENSION, ALDOSTERONE EXCESS, AND LOW PLASMA-RENIN [J].
BROWN, JJ ;
ROBERTSON, JI ;
HAYWOOD, E ;
LEVER, AF ;
FERRISS, JB ;
FRASER, R ;
DAVIES, DL .
BMJ-BRITISH MEDICAL JOURNAL, 1972, 2 (5816) :729-+
[2]   Hyperaldosteronism among with resistant black and white subjects hypertension [J].
Calhoun, DA ;
Nishizaka, MK ;
Zaman, MA ;
Thakkar, RB ;
Weissmann, P .
HYPERTENSION, 2002, 40 (06) :892-896
[3]   EFFECT OF SPIRONOLACTONE IN HYPERTENSIVE PATIENTS [J].
CRANE, MG ;
HARRIS, JJ .
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1970, 260 (06) :311-+
[4]   Prevention of cardiovascular events with an antihypertensive regimen of amlodipine adding perindopril as required versus atenolol adding bendroflumethiazide as required, in the Anglo-Scandinavian Cardiac Outcomes Trial-Blood Pressure Lowering Arm (ASCOT-BPLA):: a multicentre randomised controlled trial [J].
Dahlöf, B ;
Sever, PS ;
Poulter, NR ;
Wedel, H ;
Beevers, DG ;
Caulfield, M ;
Collins, R ;
Kjeldsen, SE ;
Kristinsson, A ;
McInnes, GT ;
Mehlsen, J ;
Nieminen, M ;
O'Brien, E ;
Östergren, J .
LANCET, 2005, 366 (9489) :895-906
[5]  
FALCH DK, 1983, ACTA MED SCAND, V213, P27
[6]   Primary hyperaldosteronism in essential hypertensives:: Prevalence, biochemical profile, and molecular biology [J].
Fardella, CE ;
Mosso, L ;
Gómez-Sánchez, C ;
Cortés, P ;
Soto, J ;
Gómez, L ;
Pinto, M ;
Huete, A ;
Oestreicher, E ;
Foradori, A ;
Montero, J .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (05) :1863-1867
[7]   TREATMENT OF LOW-RENIN (PRIMARY) HYPER-ALDOSTERONISM [J].
FERRISS, JB ;
BEEVERS, DG ;
BODDY, K ;
BROWN, JJ ;
DAVIES, DL ;
FRASER, R ;
KREMER, D ;
LEVER, AF ;
ROBERTSON, JIS .
AMERICAN HEART JOURNAL, 1978, 96 (01) :97-109
[8]   HIGH-INCIDENCE OF PRIMARY ALDOSTERONISM IN 199 PATIENTS REFERRED WITH HYPERTENSION [J].
GORDON, RD ;
STOWASSER, M ;
TUNNY, TJ ;
KLEMM, SA ;
RUTHERFORD, JC .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 1994, 21 (04) :315-318
[9]   Prevalence of primary hyperaldosteronism assessed by aldosterone/renin ratio and spironolactone testing [J].
Hood, S ;
Cannon, J ;
Foo, R ;
Brown, M .
CLINICAL MEDICINE, 2005, 5 (01) :55-60
[10]   EFFICACY AND TOLERANCE OF SPIRONOLACTONE IN ESSENTIAL-HYPERTENSION [J].
JEUNEMAITRE, X ;
CHATELLIER, G ;
KREFTJAIS, C ;
CHARRU, A ;
DEVRIES, C ;
PLOUIN, PF ;
CORVOL, P ;
MENARD, J .
AMERICAN JOURNAL OF CARDIOLOGY, 1987, 60 (10) :820-825