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Published on: October 12, 2017
Reduced paraoxonase 1 activity as a marker for severe coronary artery disease
Chiyan Zhou1, Jia Cao, Liang Shang
1Department of Biochemistry and Molecular Biology, Wuhan University School of Medicine, Wuhan, Hubei 430071, China.
Insights
Plasma paraoxonase-1 (PON1) activity is lower in patients with coronary artery disease (CAD). Lower PON1 levels correlate with increased atherosclerosis severity, suggesting PON1 may serve as a biomarker for CAD progression.
Area of Science:
- Biochemistry
- Cardiovascular Medicine
- Immunology
Background:
- Paraoxonase-1 (PON1) is an HDL-associated enzyme with potential anti-atherogenic properties.
- Atherosclerosis is a chronic inflammatory disease characterized by plaque buildup in arteries.
Purpose of the Study:
- To investigate the relationship between plasma PON1 activity and the progression of atherosclerosis and coronary artery disease (CAD).
Main Methods:
- Collected fasting blood samples from female apolipoprotein E-deficient (apoE(-/-)) mice and 149 patients undergoing coronary angiography.
- Measured biochemical parameters, including plasma PON1 activity.
- Assessed CAD severity using the Gensini score (GSS).
Main Results:
- Aged apoE(-/-) mice exhibited lower PON1 activity, negatively correlated with atherosclerotic lesion size and inflammatory markers (IL-6, TNF-α).
- In patients, PON1 activity correlated with age, sex, HDL-cholesterol, apolipoprotein AI, and hs-CRP.
- PON1 activity was significantly lower in the CAD group and further reduced in severe CAD (GSS > 40) compared to mild/moderate CAD.
- A significant negative correlation was found between PON1 activity and GSS (r = -0.393, P < 0.001).
Conclusions:
- Plasma PON1 activity is reduced in patients with CAD and correlates negatively with disease severity.
- PON1 activity may serve as a potential biomarker for assessing the severity of coronary artery disease.
Abstract:
Paraoxonase-1 (PON1), a high-density-lipoprotein- (HDL-) associated enzyme, has the potential to protect against atherogenesis. We examine the relationships between plasma PON1 activity and the progression of atherosclerosis as well as coronary artery disease (CAD). Fasting blood samples were collected from female apolipoprotein E-deficient (apoE(-/-)) mice and 149 patients undergoing coronary angiography for the biochemical parameters measurement. The severity of CAD was defined using angiographic Gensini score (GSS). Compared to 3-month-old apoE(-/-) mice, aged mice had significantly lower PON1 activity, which is negatively correlated with the size of atherosclerotic lesion and plasma interleukin-6 (IL-6) and tumor necrosis factor α (TNF- α ) levels. In study patients, PON1 activity was correlated with age, sex, and HDL-cholesterol, apolipoprotein AI, and high-sensitivity C-reactive protein (hs-CRP) levels and was significantly lower in CAD group than that in non-CAD control group. Interestingly, PON1 activity in severe CAD group (GSS > 40) was further significantly reduced compared to those in mild and moderate subgroups (GSS ≤ 40) (P < 0.01). There is a significant correlation between PON1 activity and the severity of CAD as assessed by GSS (r = -0.393, P < 0.001). PON1 activity may be a potential biomarker for the severity of CAD.
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