Journal of Lipid Research (Jun 2009)

Association of the novel cardiovascular risk factors paraoxonase 1 and cystatin C in type 2 diabetes*[S]

  • Philip W. Connelly,
  • Bernard Zinman,
  • Graham F. Maguire,
  • Mary Mamakeesick,
  • Stewart B. Harris,
  • Robert A. Hegele,
  • Ravi Retnakaran,
  • Anthony J.G. Hanley

Journal volume & issue
Vol. 50, no. 6
pp. 1216 – 1222

Abstract

Read online

Paraoxonase 1 (PON1) has been reported to be associated with proteinuria in subjects with type 2 diabetes mellitus (T2DM). Plasma cystatin C is more accurate than creatinine for identifying stage 3 kidney disease in T2DM. We tested the hypothesis that PON1 and cystatin C would be associated in T2DM subjects from an Aboriginal Canadian community, who are at high risk for the development of nephropathy. PON1 A(-162)G and PON2 Ala148Gly genotypes, cystatin C, HbA1c, high density lipoprotein cholesterol (HDLC), waist circumference (waist), and duration of diabetes were included in the regression analysis with loge (ln) of PON1 mass as the dependent variable. A regression model including PON2 Ala148Gly genotype, HDLC, and ln cystatin C explained 25.8% of the variance in PON1 mass. Conversely, waist, age, ln HbA1c, ln duration of diabetes, and ln PON1 mass, but not PON2 genotype, explained 38% of the variance in cystatin C. Subjects with cystatin C estimated glomerular filtration rate (eGFR) 60 ml/min per 1.73 m2. The lower mass of PON1, an anti-inflammatory HDL-associated enzyme, in T2DM with cystatin C-eGFR <60 ml/min per 1.73 m2 may contribute to their increased risk for cardiovascular disease.

Keywords