Aliskiren, Enalapril, or Aliskiren and Enalapril in Heart Failure

被引:184
作者
McMurray, John J. V. [1 ]
Krum, Henry [3 ]
Abraham, William T. [4 ]
Dickstein, Kenneth [5 ,6 ]
Kober, Lars V. [7 ]
Desai, Akshay S. [8 ]
Solomon, Scott D. [8 ]
Greenlaw, Nicola [2 ]
Ali, M. Atif [9 ]
Chiang, Yanntong [9 ]
Shao, Qing [9 ]
Tarnesby, Georgia [9 ]
Massie, Barry M. [10 ]
机构
[1] Univ Glasgow, British Heart Fdn, Cardiovasc Res Ctr, Glasgow G12 8TA, Lanark, Scotland
[2] Univ Glasgow, Robertson Ctr Biostat, Glasgow, Lanark, Scotland
[3] Monash Univ, Sch Publ Hlth & Prevent Med, Ctr Cardiovasc Res & Educ Therapeut, Melbourne, Vic 3004, Australia
[4] Ohio State Univ, Davis Heart & Lung Res Inst, Div Cardiovasc Med, Columbus, OH 43210 USA
[5] Stavanger Univ Hosp, Stavanger, Norway
[6] Univ Bergen, Inst Internal Med, Bergen, Norway
[7] Copenhagen Univ Hosp, Rigshosp, Copenhagen, Denmark
[8] Brigham & Womens Hosp, Div Cardiovasc, 75 Francis St, Boston, MA 02115 USA
[9] Novartis Pharmaceut, Basel, Switzerland
[10] Univ Calif San Francisco, San Francisco, CA 94143 USA
关键词
VENTRICULAR SYSTOLIC FUNCTION; CONVERTING-ENZYME INHIBITORS; RANDOMIZED-TRIAL; MINIMIZE OUTCOMES; RENIN INHIBITOR; ATMOSPHERE; VALSARTAN; MORTALITY; SURVIVAL; CANDESARTAN;
D O I
10.1056/NEJMoa1514859
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Among patients with chronic heart failure, angiotensin-converting-enzyme (ACE) inhibitors reduce mortality and hospitalization, but the role of a renin inhibitor in such patients is unknown. We compared the ACE inhibitor enalapril with the renin inhibitor aliskiren (to test superiority or at least noninferiority) and with the combination of the two treatments (to test superiority) in patients with heart failure and a reduced ejection fraction. METHODS After a single-blind run-in period, we assigned patients, in a double-blind fashion, to one of three groups: 2336 patients were assigned to receive enalapril at a dose of 5 or 10 mg twice daily, 2340 to receive aliskiren at a dose of 300 mg once daily, and 2340 to receive both treatments (combination therapy). The primary composite outcome was death from cardiovascular causes or hospitalization for heart failure. RESULTS After a median follow-up of 36.6 months, the primary outcome occurred in 770 patients (32.9%) in the combination-therapy group and in 808 (34.6%) in the enalapril group (hazard ratio, 0.93; 95% confidence interval [ CI], 0.85 to 1.03). The primary outcome occurred in 791 patients (33.8%) in the aliskiren group (hazard ratio vs. enalapril, 0.99; 95% CI, 0.90 to 1.10); the prespecified test for noninferiority was not met. There was a higher risk of hypotensive symptoms in the combination-therapy group than in the enalapril group (13.8% vs. 11.0%, P = 0.005), as well as higher risks of an elevated serum creatinine level (4.1% vs. 2.7%, P = 0.009) and an elevated potassium level (17.1% vs. 12.5%, P<0.001). CONCLUSIONS In patients with chronic heart failure, the addition of aliskiren to enalapril led to more adverse events without an increase in benefit. Noninferiority was not shown for aliskiren as compared with enalapril.
引用
收藏
页码:1521 / 1532
页数:12
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