Urinary Metabolomic Markers of Protein Glycation, Oxidation, and Nitration in Early-Stage Decline in Metabolic, Vascular, and Renal Health

Oxid Med Cell Longev. 2019 Nov 19:2019:4851323. doi: 10.1155/2019/4851323. eCollection 2019.

Abstract

Glycation, oxidation, nitration, and crosslinking of proteins are implicated in the pathogenic mechanisms of type 2 diabetes, cardiovascular disease, and chronic kidney disease. Related modified amino acids formed by proteolysis are excreted in urine. We quantified urinary levels of these metabolites and branched-chain amino acids (BCAAs) in healthy subjects and assessed changes in early-stage decline in metabolic, vascular, and renal health and explored their diagnostic utility for a noninvasive health screen. We recruited 200 human subjects with early-stage health decline and healthy controls. Urinary amino acid metabolites were determined by stable isotopic dilution analysis liquid chromatography-tandem mass spectrometry. Machine learning was applied to optimise and validate algorithms to discriminate between study groups for potential diagnostic utility. Urinary analyte changes were as follows: impaired metabolic health-increased N ε -carboxymethyl-lysine, glucosepane, glutamic semialdehyde, and pyrraline; impaired vascular health-increased glucosepane; and impaired renal health-increased BCAAs and decreased N ε -(γ-glutamyl)lysine. Algorithms combining subject age, BMI, and BCAAs discriminated between healthy controls and impaired metabolic, vascular, and renal health study groups with accuracy of 84%, 72%, and 90%, respectively. In 2-step analysis, algorithms combining subject age, BMI, and urinary N ε -fructosyl-lysine and valine discriminated between healthy controls and impaired health (any type), accuracy of 78%, and then between types of health impairment with accuracy of 69%-78% (cf. random selection 33%). From likelihood ratios, this provided small, moderate, and conclusive evidence of early-stage cardiovascular, metabolic, and renal disease with diagnostic odds ratios of 6 - 7, 26 - 28, and 34 - 79, respectively. We conclude that measurement of urinary glycated, oxidized, crosslinked, and branched-chain amino acids provides the basis for a noninvasive health screen for early-stage health decline in metabolic, vascular, and renal health.

MeSH terms

  • Adult
  • Algorithms
  • Amino Acids, Branched-Chain / metabolism
  • Amino Acids, Branched-Chain / urine
  • Biomarkers / urine*
  • Body Mass Index
  • Case-Control Studies
  • Chromatography, High Pressure Liquid
  • Female
  • Glycation End Products, Advanced / urine
  • Glycosylation
  • Humans
  • Kidney / metabolism*
  • Lysine / analogs & derivatives
  • Lysine / urine
  • Male
  • Metabolic Diseases / metabolism
  • Metabolic Diseases / pathology*
  • Oxidation-Reduction
  • Severity of Illness Index
  • Tandem Mass Spectrometry
  • Tyrosine / analogs & derivatives
  • Tyrosine / urine
  • Vascular Diseases / metabolism
  • Vascular Diseases / pathology*

Substances

  • Amino Acids, Branched-Chain
  • Biomarkers
  • Glycation End Products, Advanced
  • 3-nitrotyrosine
  • Tyrosine
  • glucosepane
  • N(6)-carboxymethyllysine
  • Lysine