Cells (May 2022)

Metabolomic Profiling in Patients with Heart Failure and Exercise Intolerance: Kynurenine as a Potential Biomarker

  • Tarek Bekfani,
  • Mohamed Bekhite,
  • Sophie Neugebauer,
  • Steffen Derlien,
  • Ali Hamadanchi,
  • Jenny Nisser,
  • Marion S. Hilse,
  • Daniela Haase,
  • Tom Kretzschmar,
  • Mei-Fang Wu,
  • Michael Lichtenauer,
  • Michael Kiehntopf,
  • Stephan von Haehling,
  • Peter Schlattmann,
  • Gabriele Lehmann,
  • Marcus Franz,
  • Sven Möbius-Winkler,
  • Christian Schulze

DOI
https://doi.org/10.3390/cells11101674
Journal volume & issue
Vol. 11, no. 10
p. 1674

Abstract

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Aims: Metabolic and structural perturbations in skeletal muscle have been found in patients with heart failure (HF) both with preserved (HFpEF) and reduced (HFrEF) ejection fraction in association with reduced muscle endurance (RME). We aimed in the current study to create phenotypes for patients with RME and HFpEF compared to RME HFrEF according to their metabolomic profiles and to test the potential of Kynurenine (Kyn) as a marker for RME. Methods: Altogether, 18 HFrEF, 17 HFpEF, and 20 healthy controls (HC) were prospectively included in the current study. The following tests were performed on all participants: isokinetic muscle function tests, echocardiography, spiroergometry, and varied blood tests. Liquid chromatography tandem mass spectrometry was used to quantify metabolites in serum. Results: Except for aromatic and branched amino acids (AA), patients with HF showed reduced AAs compared to HC. Further perturbations were elevated concentrations of Kyn and acylcarnitines (ACs) in HFpEF and HFrEF patients (p p p = 0.001). Conclusions: RME in patients with HFpEF vs. HFrEF proved to have different metabolomic profiles suggesting varied pathophysiology. Kyn might be a promising biomarker for patients with HF and RME.

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