Dietary cholesterol increases paraoxonase 1 enzyme activity

J Lipid Res. 2012 Nov;53(11):2450-8. doi: 10.1194/jlr.P030601. Epub 2012 Aug 15.

Abstract

HDL-associated paraoxonase 1 (PON1) activity has been consistently associated with cardiovascular and other diseases. Vitamins C and E intake have previously been positively associated with PON1 in a subset of the Carotid Lesion Epidemiology and Risk (CLEAR) cohort. The goal of this study was to replicate these findings and determine whether other nutrient intake affected PON1 activity. To predict nutrient and mineral intake values, 1,402 subjects completed a standardized food frequency survey of their dietary habits over the past year. Stepwise regression was used to evaluate dietary and covariate effects on PON1 arylesterase activity. Five dietary components, cholesterol (P < 2.0 × 10(-16)), alcohol (P = 8.51 × 10(-8)), vitamin C (P = 7.97 × 10(-5)), iron (P = 0.0026), and folic acid (0.037) were independently predictive of PON1 activity. Dietary cholesterol was positively associated and predicted 5.5% of PON1 activity, second in variance explained. This study presents a novel finding of dietary cholesterol, iron, and folic acid predicting PON1 activity in humans and confirms prior reported associations, including that with vitamin C. Identifying and understanding environmental factors that affect PON1 activity is necessary to understand its role and that of HDL in human disease.

Publication types

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

MeSH terms

  • Aged
  • Apolipoprotein A-I / blood
  • Aryldialkylphosphatase / genetics
  • Aryldialkylphosphatase / metabolism*
  • Cholesterol / blood
  • Cholesterol, Dietary / pharmacology*
  • Enzyme Activation / drug effects
  • Female
  • Genotype
  • Humans
  • Lipoproteins, HDL / blood
  • Lipoproteins, VLDL / blood
  • Male
  • Middle Aged

Substances

  • APOA1 protein, human
  • Apolipoprotein A-I
  • Cholesterol, Dietary
  • Lipoproteins, HDL
  • Lipoproteins, VLDL
  • Cholesterol
  • Aryldialkylphosphatase