Free fatty acid depletion acutely decreases cardiac work and efficiency in cardiomyopathic heart failure

被引:201
作者
Tuunanen, Helena
Engblom, Erik
Naum, Alexandru
Nagren, Kjell
Hesse, Birger
Airaksinen, Juhani
Nuutila, Pirjo
Iozzo, Patricia
Ukkonen, Heikki
Opie, Lionel H.
Knuuti, Juhani
机构
[1] Turku Univ, Cent Hosp, Turku PET Ctr, FIN-20520 Turku, Finland
[2] Turku Univ, Cent Hosp, Dept Med, FIN-20520 Turku, Finland
[3] Univ Cape Town, Dept Med, Hatter Heart Res Inst, ZA-7925 Cape Town, South Africa
[4] Copenhagen Univ Hosp, Dept Clin Physiol & Nucl Med, Copenhagen, Denmark
[5] CNR, Inst Clin Physiol, Pisa, Italy
关键词
cardiomyopathy; fatty acids; heart failure; metabolism;
D O I
10.1161/CIRCULATIONAHA.106.645184
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - Metabolic modulators that enhance myocardial glucose metabolism by inhibiting free fatty acid (FFA) metabolism may improve cardiac function in heart failure patients. We studied the effect of acute FFA withdrawal on cardiac function in patients with heart failure caused by idiopathic dilated cardiomyopathy (IDCM). Methods and Results - Eighteen fasting nondiabetic patients with IDCM (14 men, 4 women, aged 58.8 +/- 8.0 years, ejection fraction 33 +/- 8.8%) and 8 matched healthy controls underwent examination of myocardial perfusion and oxidative and FFA metabolism, before and after acute reduction of serum FFA concentrations by acipimox, an inhibitor of lipolysis. Metabolism was monitored by positron emission tomography and [O-15]H2O, [C-11]acetate, and [C-11]palmitate. Left ventricular function and myocardial work were echocardiographically measured, and efficiency of forward work was calculated. Acipimox decreased myocardial FFA uptake by > 80% in both groups. Rate - pressure product and myocardial perfusion remained unchanged, whereas stroke volume decreased similarly in both groups. In the healthy controls, reduced cardiac work was accompanied by decreased oxidative metabolism (from 0.071 +/- 0.019 to 0.055 +/- 0.016 min(-1), P < 0.01). In IDCM patients, cardiac work fell, whereas oxidative metabolism remained unchanged and efficiency fell (from 35.4 +/- 12.6 to 31.6 +/- 13.3 mm Hg (.) L (.) g(-1), P < 0.05). Conclusions - Acutely decreased serum FFA depresses cardiac work. In healthy hearts, this is accompanied by parallel decrease in oxidative metabolism, and myocardial efficiency is preserved. In failing hearts, FFA depletion did not downregulate oxidative metabolism, and myocardial efficiency deteriorated. Thus, failing hearts are unexpectedly more dependent than healthy hearts on FFA availability. We propose that both glucose and fatty acid oxidation are required for optimal function of the failing heart.
引用
收藏
页码:2130 / 2137
页数:8
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