Targeted metabolomic analysis of serum amino acids in the adult Fontan patient with a dominant left ventricle

Sci Rep. 2020 Jun 2;10(1):8930. doi: 10.1038/s41598-020-65852-x.

Abstract

Growing interest lies in the assessment of the metabolic status of patients with a univentricular circulation after Fontan operation, especially in changes of amino acid metabolism. Using targeted metabolomic examinations, we investigated amino acid metabolism in a homogeneous adult Fontan-patient group with a dominant left ventricle, seeking biomarker patterns that might permit better understanding of Fontan pathophysiology and early detection of subtle ventricular or circulatory dysfunction. We compared serum amino acid levels (42 analytes; AbsoluteIDQ p180 kit, Biocrates Life Sciences, Innsbruck, Austria) in 20 adult Fontan patients with a dominant left ventricle and those in age- and sex-matched biventricular controls. Serum concentrations of asymmetric dimethylarginine, methionine sulfoxide, glutamic acid, and trans-4-hydroxyproline and the methionine sulfoxide/methionine ratio (Met-SO/Met) were significantly higher and serum concentrations of asparagine, histidine, taurine, and threonine were significantly lower in patients than in controls. Met-SO/Met values exhibited a significant negative correlation with oxygen uptake during exercise. The alterations in amino acid metabolome that we found in Fontan patients suggest links between Fontan pathophysiology, altered cell energy metabolism, oxidative stress, and endothelial dysfunction like those found in biventricular patients with congestive heart failure. Studies of extended amino acid metabolism may allow better understanding of Fontan pathophysiology that will permit early detection of subtle ventricular or circulatory dysfunction in Fontan patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / blood*
  • Amino Acids / metabolism
  • Case-Control Studies
  • Coronary Circulation / physiology
  • Female
  • Fontan Procedure* / adverse effects
  • Heart Defects, Congenital / blood
  • Heart Defects, Congenital / metabolism
  • Heart Defects, Congenital / surgery
  • Humans
  • Male
  • Metabolomics
  • Oxidative Stress
  • Ventricular Dysfunction, Left / blood*
  • Ventricular Dysfunction, Left / metabolism
  • Young Adult

Substances

  • Amino Acids