Effect of high-dose atorvastatin on hospitalizations for heart failure - Subgroup analysis of the treating to new targets (TNT) study

被引:140
作者
Khush, Kiran K.
Waters, David D.
Bittner, Vera
Deedwania, Prakash C.
Kastelein, John J. P.
Lewis, Sandra J.
Wenger, Nanette K.
机构
[1] Univ Calif San Francisco, Sch Med, Div Cardiol, San Francisco, CA 94143 USA
[2] Univ Alabama, Dept Med, Div Cardiovasc Dis, Birmingham, AL 35294 USA
[3] Univ Calif San Francisco, Sch Med, Fresno, CA USA
[4] Univ Amsterdam, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
[5] Portland Cardiovasc Inst, Portland, OR USA
[6] Emory Univ, Sch Med, Atlanta, GA 30322 USA
关键词
atorvastatin; cholesterol; coronary disease; heart failure; hospitalizations; lipids; statins;
D O I
10.1161/CIRCULATIONAHA.106.625574
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - Statins reduce the rate of major cardiovascular events in high-risk patients, but their potential benefit as treatment for heart failure ( HF) is less clear. Methods and Results - Patients (n=10 001) with stable coronary disease were randomized to treatment with atorvastatin 80 or 10 mg/d and followed up for a median of 4.9 years. A history of HF was present in 7.8% of patients. A known ejection fraction < 30% and advanced HF were exclusion criteria for the study. A predefined secondary end point of the study was hospitalization for HF. The incidence of hospitalization for HF was 2.4% in the 80-mg arm and 3.3% in the 10-mg arm (hazard ratio, 0.74; 95% confidence interval, 0.59 to 0.94; P=0.0116). The treatment effect of the higher dose was more marked in patients with a history of HF: 17.3% versus 10.6% in the 10- and 80-mg arms, respectively (hazard ratio, 0.59; 95% confidence interval, 0.4 to 0.88; P=0.009). Among patients without a history of HF, the rates of hospitalization for HF were much lower: 1.8% in the 80-mg group and 2.0% in the 10-mg group (hazard ratio, 0.87; 95% confidence interval, 0.64 to 1.16; P=0.34). Only one third of patients hospitalized for HF had evidence of preceding angina or myocardial infarction during the study period. Blood pressure was almost identical during follow-up in the treatment groups. Conclusions - Compared with a lower dose, intensive treatment with atorvastatin in patients with stable coronary disease significantly reduces hospitalizations for HF. In a post hoc analysis, this benefit was observed only in patients with a history of HF. The mechanism accounting for this benefit is unlikely to be due primarily to a reduction in interim coronary events or differences in blood pressure.
引用
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页码:576 / 583
页数:8
相关论文
共 33 条
[1]  
Ashton Emma, 2003, Heart Fail Monit, V3, P82
[2]   Neutral effect on markers of heart failure, inflammation, endothelial activation and function, and vagal tone after high-dose HMG-CoA reductase inhibition in non-diabetic patients with non-ischemic cardiomyopathy and average low-density lipoprotein level [J].
Bleske, BE ;
Nicklas, JM ;
Bard, RL ;
Brook, RD ;
Gurbel, PA ;
Bliden, KP ;
Rajagopalan, S ;
Pitt, B .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2006, 47 (02) :338-341
[3]   Randomized, double-blind, placebo-controlled, pilot trial of infliximab, a chimeric monoclonal antibody to tumor necrosis factor-α, in patients with moderate-to-severe heart failure -: Results of the Anti-TNF Therapy Against Congestive Heart Failure (ATTACH) trial [J].
Chung, ES ;
Packer, M ;
Lo, KH ;
Fasanmade, AA ;
Willerson, JT .
CIRCULATION, 2003, 107 (25) :3133-3140
[4]   Drug therapy - The management of chronic heart failure [J].
Cohn, JN .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (07) :490-498
[5]   Amelioration of angiotensin II-induced cardiac injury by a 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor [J].
Dechend, R ;
Fiebeler, A ;
Park, JK ;
Muller, DN ;
Theuer, J ;
Mervaala, E ;
Bieringer, M ;
Gulba, D ;
Dietz, R ;
Luft, FC ;
Haller, H .
CIRCULATION, 2001, 104 (05) :576-581
[6]   Simvastatin inhibits the monocyte expression of proinflammatory cytokines in patients with hypercholesterolemia [J].
Ferro, D ;
Parrotto, S ;
Basili, S ;
Alessandri, C ;
Violi, F .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2000, 36 (02) :427-+
[7]   Pravastatin down-regulates inflammatory mediators in human monocytes in vitro [J].
Grip, O ;
Janciauskiene, S ;
Lindgren, S .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2000, 410 (01) :83-92
[8]   Fluvastatin, a 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor, attenuates left ventricular remodeling and failure after experimental myocardial infarction [J].
Hayashidani, S ;
Tsutsui, H ;
Shiomi, T ;
Suematsu, N ;
Kinugawa, S ;
Ide, T ;
Wen, J ;
Takeshita, A .
CIRCULATION, 2002, 105 (07) :868-873
[9]   Low serum total cholesterol is associated with marked increase in mortality in advanced heart failure [J].
Horwich, TB ;
Hamilton, MA ;
MacLellan, WR ;
Fonarow, GC .
JOURNAL OF CARDIAC FAILURE, 2002, 8 (04) :216-224
[10]   Decreased activity of the L-arginine-nitric oxide metabolic pathway in patients with congestive heart failure [J].
Katz, SD ;
Khan, T ;
Zeballos, GA ;
Mathew, L ;
Potharlanka, P ;
Knecht, M ;
Whelan, J .
CIRCULATION, 1999, 99 (16) :2113-2117