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Synapse
January 1, 2016Cardiac failure review30 citationsOpen Access

Deranged cardiac metabolism and the pathogenesis of heart failure

GFGabriele Fragasso

Structured PICO

Does metabolic therapy (shifting energy substrate preference from fatty acids to glucose) improve clinical symptoms and cardiac function in patients with heart failure?

P
Population
Patients with heart failure
I
Intervention
Metabolic therapy (shifting energy substrate preference away from fatty acid metabolism towards glucose metabolism / partial inhibition of fatty acid oxidation)

Metabolic modulation, specifically shifting cardiac energy substrate preference from fatty acids to glucose, is proposed as a potential adjunctive therapy for heart failure.

Abstract

Activation of the neuro-hormonal system is a pathophysiological consequence of heart failure. Neuro-hormonal activation promotes metabolic changes, such as insulin resistance, and determines an increased use of non-carbohydrate substrates for energy production. Fasting blood ketone bodies as well as fat oxidation are increased in patients with heart failure, yielding a state of metabolic inefficiency. The net result is additional depletion of myocardial adenosine triphosphate, phosphocreatine and creatine kinase levels with further decreased efficiency of mechanical work. In this context, manipulation of cardiac energy metabolism by modification of substrate use by the failing heart has produced positive clinical results. The results of current research support the concept that shifting the energy substrate preference away from fatty acid metabolism and towards glucose metabolism could be an effective adjunctive treatment in patients with heart failure. The additional use of drugs able to partially inhibit fatty acids oxidation in patients with heart failure may therefore yield a significant protective effect for clinical symptoms and cardiac function improvement, and simultaneously ameliorate left ventricular remodelling. Certainly, to clarify the exact therapeutic role of metabolic therapy in heart failure, a large multicentre, randomised controlled trial should be performed.

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Cite This Study

Gabriele Fragasso (2016) studied this question.

synapsesocial.com/papers/6a220b2d2e065aea60493167https://doi.org/10.15420/cfr.2016:5:2
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Metabolic responses to graded exercise in chronic heart failure1993 · 16 citations
  2. 2Resting energy expenditure in chronic cardiac failure1991 · 86 citations
  3. 3A Randomized Clinical Trial of Trimetazidine, a Partial Free Fatty Acid Oxidation Inhibitor, in Patients With Heart Failure2006 · 270 citations
  4. 4Angiotensin II downregulates the fatty acid oxidation pathway in adult rat cardiomyocytes via release of tumour necrosis factor-α2009 · 61 citations
  5. 5Influence of central inhibition of sympathetic nervous activity on myocardial metabolism in chronic heart failure: acute effects of the imidazoline I1-receptor agonist moxonidine2006 · 18 citations