Relation of Disease Pathogenesis and Risk Factors to Heart Failure With Preserved or Reduced Ejection Fraction Insights From the Framingham Heart Study of the National Heart, Lung, and Blood Institute

被引:533
作者
Lee, Douglas S. [2 ,3 ]
Gona, Philimon [1 ,4 ]
Vasan, Ramachandran S. [1 ,5 ,6 ]
Larson, Martin G. [1 ,4 ]
Benjamin, Emelia J. [1 ,5 ,6 ]
Wang, Thomas J. [1 ,7 ]
Tu, Jack V. [2 ,8 ]
Levy, Daniel [1 ,9 ]
机构
[1] NHLBI, Framingham Heart Study, Framingham, MA 01702 USA
[2] Inst Clin Evaluat Sci, Toronto, ON, Canada
[3] Univ Toronto, Univ Hlth Network, Toronto, ON, Canada
[4] Boston Univ, Dept Math & Stat, Boston, MA 02215 USA
[5] Boston Univ, Sch Med, Cardiol Sect, Boston, MA 02118 USA
[6] Boston Univ, Sch Med, Dept Prevent Med & Epidemiol, Boston, MA 02118 USA
[7] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Div Cardiol, Boston, MA USA
[8] Univ Toronto, Sunnybrook Hlth Sci Ctr, Toronto, ON, Canada
[9] NHLBI, Ctr Populat Studies, Bethesda, MD 20892 USA
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
coronary disease; epidemiology; heart diseases; heart failure; hypertension; mortality; ventricles; CLINICAL DETERMINANTS; QRS DURATION; MORTALITY; DYSFUNCTION; PREVALENCE; SPECTRUM; OUTCOMES; GENDER;
D O I
10.1161/CIRCULATIONAHA.108.815944
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-The contributions of risk factors and disease pathogenesis to heart failure with preserved ejection fraction (HFPEF) versus heart failure with reduced ejection fraction (HFREF) have not been fully explored. Methods and Results-We examined clinical characteristics and risk factors at time of heart failure onset and long-term survival in Framingham Heart Study participants according to left ventricular ejection fraction <= 45% (n = 314; 59%) versus >45% (n = 220; 41%) and hierarchical causal classification. Heart failure was attributed to coronary heart disease in 278 participants (52%), valvular heart disease in 42 (8%), hypertension in 140 (26%), or other/unknown causes in 74 (14%). Multivariable predictors of HFPEF (versus HFREF) included elevated systolic blood pressure (odds ratio [OR] = 1.13 per 10 mm Hg; 95% confidence interval [CI], 1.04 to 1.22), atrial fibrillation (OR = 4.23; 95% CI, 2.38 to 7.52), and female sex (OR = 2.29; 95% CI, 1.35 to 3.90). Conversely, prior myocardial infarction (OR = 0.32; 95% CI, 0.19 to 0.53) and left bundle-branch block QRS morphology (OR = 0.21; 95% CI, 0.10 to 0.46) reduced the odds of HFPEF. Long-term prognosis was grim, with a median survival of 2.1 years (5-year mortality rate, 74%), and was equally poor in men and women with HFREF or HFPEF. Conclusions-Among community patients with new-onset heart failure, there are differences in causes and time-of-onset clinical characteristics between those with HFPEF versus HFREF. In people with HFREF, mortality is increased when coronary heart disease is the underlying cause. These findings suggest that heart failure with reduced left ventricular systolic function and heart failure with preserved left ventricular systolic function are partially distinct entities, with potentially different approaches to early detection and prevention. (Circulation. 2009; 119: 3070-3077.)
引用
收藏
页码:3070 / 3077
页数:8
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