Cell Biochemistry and Biophysics

, Volume 61, Issue 2, pp 461–466 | Cite as

Plasma Paraoxonase-1, Oxidized Low-Density Lipoprotein and Lipid Peroxidation Levels in Gout Patients

  • Xing-Liang Jiang
  • Min Li
  • Jing-Guo Zhou
  • Qi-Bin Yang
  • Li-Jun Du
  • Juan Du
Translational Biomedical Research


Gout patients have a high incidence of atherosclerotic coronary heart disease. Low serum paraoxonase (PON) activity is considered a risk factor for atherosclerosis. The relationships among paraoxonase-1 (PON1) activity, oxidative stress parameters, and atherosclerosis in gout is not known. Therefore, we determined the plasma levels of malondialdehyde (MDA), oxidized low-density lipoprotein (Ox-LDL), and activities of PON1/superoxide dismutase (SOD) activities in 49 gout patients (mean age 44.2 ± 7.0 years) and 42 healthy, age-matched controls (mean age 45.0 ± 9.3 years). PON1 was measured spectrophotometrically, MDA by thiobarbituric acid method, SOD by Griess reaction, and Ox-LDL by sandwich ELISA. Lipid and other biochemical parameters were determined by routine laboratory methods. In gout patients, PON1/SOD activities and MDA/Ox-LDL levels were 131.3 ± 25.3/75.3 ± 28.9 kU l−1 and 6.12 ± 1.67 nmol ml−1/690.1 ± 180.2 μg l−1, respectively. In controls, these were 172.5 ± 27.8/94.0 ± 26.3 kU l−1 and 4.10 ± 1.25 nmol ml−1/452.3 ± 152.1 μg l−1, respectively. Thus, in gout patients, there was a significant decrease in PON1 (P < 0.01) and SOD (P < 0.05) activities, and an increase in MDA (P < 0.01) and Ox-LDL (P < 0.01) levels compared with controls. PON1 activity correlated positively with SOD (P < 0.05), and negatively with MDA (P < 0.01) and Ox-LDL (P < 0.01). These results suggest that gout patients were in a state of oxidative stress and the protective effects of HDL against atherosclerosis maybe dependent on PON1 activity. These findings may explain in part the reported increase in cardiovascular mortality in gout patients.


Gout Paraoxonase-1 Oxidized low-density lipoprotein Lipid peroxidation 



The authors thank the Department of Health of Sichuan Province for the financial support (Grant #20090143), for this study.


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Copyright information

© Springer Science+Business Media, LLC 2011

Authors and Affiliations

  • Xing-Liang Jiang
    • 1
  • Min Li
    • 2
  • Jing-Guo Zhou
    • 2
  • Qi-Bin Yang
    • 2
  • Li-Jun Du
    • 2
  • Juan Du
    • 1
  1. 1.Department of Medical Laboratory ScienceAffiliated Hospital of North Sichuan Medical CollegeNanchongChina
  2. 2.Institute of Rheumatology and ImmunologyAffiliated Hospital of North Sichuan Medical CollegeNanchongChina

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