Key result
Elevated long-chain acylcarnitines are linked to adverse outcomes in systolic HF and decrease post-LVAD.
Why the study?
The reversibility and prognostic value of circulating metabolomic markers associated with energy homeostasis perturbations in heart failure remain unclear.
Are circulating long-chain acylcarnitine levels associated with adverse clinical outcomes in chronic heart failure and do they decrease after mechanical circulatory support?
Cohort (n=494)
randomized
Are circulating long-chain acylcarnitine levels associated with adverse clinical outcomes in chronic heart failure and do they decrease after mechanical circulatory support?
Elevated long-chain acylcarnitines are associated with adverse outcomes in chronic systolic heart failure and are partially reversible with mechanical circulatory support.
BACKGROUND: Heart failure (HF) is characterized by perturbations in energy homeostasis and metabolism. The reversibility and prognostic value of circulating markers associated with these changes remain unclear. OBJECTIVES: This study sought to describe the metabolomic profiles of patients along the spectrum of systolic HF, determine their association with adverse outcomes in a clinical trial of HF, and evaluate whether identified metabolites change with treatment for end-stage systolic HF. METHODS: To assess association of metabolites with clinical outcomes, we evaluated a population of 453 chronic systolic HF patients who had been randomized to exercise training versus usual care. To assess change in metabolites with mechanical circulatory support, 41 patients with end-stage HF who underwent left ventricular assist device (LVAD) placement were studied. Targeted, quantitative profiling of 60 metabolites using tandem flow injection mass spectrometry was performed on frozen plasma samples obtained prior to randomization, as well as prior to and ≥90 days post-placement in the LVAD group. Principal components analysis was used for data reduction. RESULTS: Five principal components analysis-derived factors were significantly associated with peak Vo2 levels at baseline in fully adjusted models. Of these, factor 5 (composed of long-chain acylcarnitines) was associated with increased risk of all 3 pre-specified clinical trial outcomes: all-cause mortality/all-cause hospitalization, all cause-hospitalization, and cardiovascular death or cardiovascular hospitalization. Individual components of factor 5 were significantly higher in patients with end-stage HF prior to LVAD placement and decreased significantly post-implantation. CONCLUSIONS: In chronic HF patients, circulating long-chain acylcarnitine metabolite levels were independently associated with adverse clinical outcomes and decreased after long-term mechanical circulatory support. These metabolites may serve as potential targets for new diagnostics or therapeutic interventions. (Exercise Training Program to Improve Clinical Outcomes in Individuals With Congestive Heart Failure; NCT00047437).
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Ahmad et al. (2016) conducted a cohort in Heart failure (n=494). Circulating long-chain acylcarnitines was evaluated on All-cause mortality/all-cause hospitalization, all cause-hospitalization, and cardiovascular death or cardiovascular hospitalization. Circulating long-chain acylcarnitines were independently associated with increased risk of adverse clinical outcomes in chronic systolic heart failure and decreased after LVAD placement.
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