Diminished antioxidant activity of high-density lipoprotein-associated proteins in chronic kidney disease

J Am Heart Assoc. 2013 Apr 4;2(2):e000104. doi: 10.1161/JAHA.112.000104.

Abstract

Background: Decreased serum arylesterase activity, catalyzed by the high-density lipoprotein-associated paraoxonase (PON)-1, is associated with increased oxidant stress and atherosclerosis risk. We sought to determine the prognostic value of serum PON-1 activity, as monitored by PON or arylesterase activities, in subjects with chronic kidney disease (CKD), particularly in relation to established cardiac biomarkers.

Methods and results: Serum arylesterase and PON activities were measured in sequential subjects with CKD (n=630; estimated glomerular filtration rate [eGFR] <60 mL/min per 1.73 m(2)) and an age- and sex-matched control group of non-CKD subjects (n=315) presenting for cardiac evaluations and prospectively followed for incident (3-year) major adverse cardiac events (composite of death, nonfatal myocardial infarction, and stroke). Serum arylesterase activity in CKD subjects was lower compared with that in non-CKD control subjects [median (interquartile range) 94 (77 to 112) versus 103 (85 to 121) μmol(L·min) per mL, P<0.001]; similarly, PON activity in CKD subjects was lower compared with that in non-CKD control subjects [median (interquartile range) 474 (275 to 936) versus 586 (301 to 1118) nmol(L·min) per mL, P<0.001]. Lower serum arylesterase (hazard ratio 1.8, 95% CI 1.26 to 2.57, P<0.01) was a predictor of poorer outcomes. After adjusting for traditional risk factors and medication use, lower serum arylesterase (hazard ratio 1.55, 95% CI 1.08 to 2.23, P<0.05) still conferred an increased risk of major adverse cardiac events at 3 years.

Conclusions: In patients with CKD, decreased serum arylesterase activity, a measure of diminished antioxidant properties of PON-1, predicts higher risk of incident long-term adverse cardiovascular events (heart attack, stroke, or death) in multivariable models adjusting for established clinical and biochemical risk factors.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Antioxidants / physiology*
  • Aryldialkylphosphatase / blood*
  • Cardiovascular Diseases / enzymology*
  • Cardiovascular Diseases / mortality
  • Cardiovascular Diseases / physiopathology
  • Case-Control Studies
  • Dyslipidemias / physiopathology
  • Enzyme Assays
  • Female
  • Follow-Up Studies
  • Humans
  • Kaplan-Meier Estimate
  • Lipoproteins, HDL / physiology*
  • Male
  • Middle Aged
  • Myocardial Infarction
  • Oxidative Stress / physiology*
  • Proportional Hazards Models
  • Prospective Studies
  • Renal Insufficiency, Chronic / enzymology*
  • Renal Insufficiency, Chronic / mortality
  • Renal Insufficiency, Chronic / physiopathology
  • Stroke

Substances

  • Antioxidants
  • Lipoproteins, HDL
  • Aryldialkylphosphatase
  • PON1 protein, human