Association of plasma metabolites and cardiac mitochondrial function with heart failure progression.

Abstract

AIMS: Plasma metabolites are prognostic in heart failure with reduced ejection fraction (HFrEF), with citric acid cycle metabolites linked to ejection fraction (EF) changes. We investigated these mechanisms in a canine chronic HFrEF model. We tested associations between changes in plasma metabolites, left ventricular (LV) end-diastolic volume and cardiomyocyte mitochondrial function. METHODS: Eighteen dogs underwent microembolization to induce moderate HFrEF (target LVEF 35%-40%). Plasma metabolites, LV size and mitochondrial function were assessed over 12&#xa0;months. RESULTS: Plasma metabolite heatmap showed acylcarnitine changes, with early alterations in organic acids and amino acids predicting later adverse LV remodelling. Using either baseline or change over time, 13 metabolites correlated with 12&#xa0;month LV enlargement. This is mostly often at 3&#xa0;months (11 of 13), notably C18:2 (r&#xa0;=&#xa0;-0.58, P&#xa0;=&#xa0;0.003) and cardiac anaplerotic substrates like glutamine (r&#xa0;=&#xa0;-0.52, P&#xa0;=&#xa0;0.009) and 3-HBA (r&#xa0;=&#xa0;-0.43, P&#xa0;=&#xa0;0.035). Impaired cardiomyocyte mitochondrial function correlated with LV enlargement (max ATP synthesis 12.7 vs. 19.9&#xa0;nmol/min/mg, P&#xa0;=&#xa0;0.0036; ADP-stimulated respiration 224 vs. 308&#xa0;nAtom O/min/mg protein; P&#xa0;=&#xa0;0.0064). Plasma metabolites correlated with mitochondrial parameters at 12&#xa0;month, particularly with MAX ATP: malate (r&#xa0;=&#xa0;-0.75, P&#xa0;<&#xa0;0.001), fumarate (r&#xa0;=&#xa0;-0.6, P&#xa0;=&#xa0;0.008) and glutamine (r&#xa0;=&#xa0;0.51, P&#xa0;=&#xa0;0.031). CONCLUSIONS: In canine HFrEF, plasma acylcarnitines, citric acid cycle or anaplerotic metabolites predicted adverse LV remodelling. LV enlargement correlated with reduced cardiomyocyte mitochondrial function, which in turn was also associated with increased citric acid cycle metabolites. Together, these data suggest impaired cardiac energetic function drives plasma metabolite associations in HFrEF progression.