Effect of heart rate reduction by ivabradine on left ventricular remodeling in the echocardiographic substudy of BEAUTIFUL

被引:74
作者
Ceconi, C. [1 ]
Freedman, S. B. [2 ]
Tardif, J. C. [3 ]
Hildebrandt, P. [4 ]
McDonagh, T. [5 ]
Gueret, P. [6 ,7 ]
Parrinello, G. [8 ]
Robertson, M. [9 ]
Steg, P. G. [10 ]
Tendera, M. [11 ]
Ford, I. [9 ]
Fox, K. [5 ]
Ferrari, R. [1 ]
机构
[1] Univ Ferrara, S Maugeri Fdn, Lumezzane, Italy
[2] Univ Sydney, Sydney Med Sch, Concord Repatriat Gen Hosp, Sydney, NSW 2006, Australia
[3] Univ Montreal, Montreal Heart Inst, Quebec City, PQ, Canada
[4] Frederiksberg Univ Hosp, Speciallaegectr, Frederiksberg, Denmark
[5] Royal Brompton Hosp, London SW3 6LY, England
[6] Hop Henri Mondor, INSERM, U955, F-94010 Creteil, France
[7] Hop Henri Mondor, AP HP, F-94010 Creteil, France
[8] Univ Brescia, Med Stat Unit, I-25121 Brescia, Italy
[9] Univ Glasgow, Robertson Ctr Biostat, Glasgow, Lanark, Scotland
[10] Univ Paris 07, INSERM, Hop Bichat Claude Bernard, AP HP,U698, Paris, France
[11] Med Univ Silesia, Katowice, Poland
关键词
Echocardiography; Ivabradine; LV function; LV remodeling; NT-proBNP; Heart rate; ACUTE MYOCARDIAL-INFARCTION; CORONARY-ARTERY-DISEASE; I-F INHIBITOR; SYSTOLIC DYSFUNCTION; DOUBLE-BLIND; FAILURE; PERINDOPRIL; CARVEDILOL; OUTCOMES; TRIAL;
D O I
10.1016/j.ijcard.2010.10.125
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: Occlusive coronary artery disease (CAD) is associated with left ventricular (LV) remodeling, LV systolic dysfunction, and heart failure. The BEAUTIFUL Echo substudy aimed to evaluate the effects of heart rate reduction with ivabradine on LV size (primary end-point: change in LV end-systolic volume index [LVESVI]) and function and the cardiac biomarker N-terminal pro-brain natriuretic peptide (NT-proBNP). Methods and results: The substudy was carried out in 86 centers participating in the BEAUTIFUL study. 2D echocardiography was performed at baseline, and after 3 and 12 months in patients with stable CAD and LV systolic dysfunction receiving ivabradine or placebo at the same time-points. All data were read and analyzed centrally. Of 525 patients completing the study, 426 had adequate echocardiographic readings (n=220 ivabradine; n=206 placebo). Treatment with ivabradine was associated with a decrease in the primary end-point LVESVI (change from baseline to last value, -1.48 +/- 13.00 mL/m(2)) versus an increase with placebo (1.85 +/- 10.54 mL/m(2)) (P=0.018). There was an increase in LV ejection fraction with ivabradine (2.00 +/- 7.02%) versus no change with placebo (0.01 +/- 6.20%) (P=0.009). Reduction in LVESVI was related to the degree of heart rate reduction with ivabradine. There were no differences in any other echocardiographic parameters or NT-proBNP. Change in LVESVI was related to the log change in NT-proBNP in the ivabradine group only (r=0.18, P=0.006). Conclusions: Our observations suggest that ivabradine may reverse detrimental LV remodeling in patients with CAD and LV systolic dysfunction. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:408 / 414
页数:7
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