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Published on: October 12, 2017
Lipoprotein lipase and premature coronary artery disease
Zhong Chen1, Genshan Ma, Xiaoli Zhang
1Department of Cardiology, Affiliated ZhongDa Hospital of Southeast University, NO. 87 Dingjiaqiao, Hunan Road, Nanjing 210009, PR China. zhongchen7498@sina.com.cn
Insights
Low lipoprotein lipase (LPL) activity and high high-sensitivity C-reactive protein (hs-CRP) predict premature coronary artery disease (CAD) in men. LPL activity is inversely correlated with hs-CRP, indicating a link between inflammation and heart disease risk.
Area of Science:
- Cardiovascular Medicine
- Lipid Metabolism
- Inflammation Research
Background:
- Premature stable coronary artery disease (CAD) is a significant health concern in male patients.
- Chronic inflammation and altered lipid metabolism, particularly lipoprotein lipase (LPL) activity, are implicated in CAD development.
- Understanding the interplay between LPL activity, inflammation, and CAD risk is crucial for effective prevention and treatment strategies.
Purpose of the Study:
- To investigate the relationship between post-heparin plasma lipoprotein lipase (LPL) activity and chronic inflammation in male patients with premature stable coronary artery disease (CAD).
- To identify predictors of premature stable CAD in male patients.
- To explore the association between LPL activity, inflammatory markers, and the severity of coronary artery stenosis.
Main Methods:
- A case-control study involving 132 male patients (< 55 years) with documented stable CAD and 130 age-matched male controls without CAD.
- Measurement of post-heparin plasma LPL activity and high-sensitivity C-reactive protein (hs-CRP) levels.
- Statistical analysis including correlation, multivariate analysis, and assessment of predictors for premature stable CAD.
Main Results:
- Patients with premature CAD exhibited significantly higher hs-CRP levels and lower LPL activity compared to controls.
- LPL activity was inversely associated with hs-CRP and triglycerides (TG), and positively associated with HDL-C.
- Higher hs-CRP, BMI, LDL-C, and hypertension were significant predictors of premature stable CAD; higher LPL activity was protective (OR 0.87). LPL activity decreased with increased coronary stenosis.
Conclusions:
- Post-heparin plasma LPL activity and hs-CRP are significant, inversely correlated predictors of premature stable CAD in male patients.
- Reduced LPL activity and elevated hs-CRP are key indicators of increased risk for premature cardiovascular events in men.
- These findings highlight the importance of assessing LPL activity and inflammatory markers in the management of male patients at risk for early-onset CAD.
Objective:
This study investigates the relationship between post-heparin plasma lipoprotein lipase (LPL) activity, chronic inflammation and premature stable coronary artery disease (CAD) in male patients.
Methods And Results:
132 male patients (< 55 years) with documented stable CAD (cases) and 130 male subjects without CAD were enrolled. Cases had higher values of high-sensitivity C-reactive protein (hs-CRP) and lower LPL activity [(5.31 +/- 3.06) mg/l vs. (2.67 +/- 1.01) mg/l, P < 0.01; (27.39 +/- 6.71) nmol x ml(-1) x min(-1) vs. (37.06 +/- 7.22) nmol x ml(-1) x min(-1), P < 0.01, respectively]. LPL activity was inversely associated with hs-CRP and triglycerides (TG), and positively associated with HDL-C (r = -0.761, P < 0.001; r = -0.339, P < 0.001; r = 0.217, P < 0.05; respectively) in cases. In multivariate analysis, higher values of hs-CRP (OR 1.45, 95% CI: 1.083-1.951; P = 0.013), BMI, LDL-C and hypertension were significant predictors of premature stable CAD in male patients. Higher LPL activity decreases risk of premature stable CAD (OR 0.87, 95% CI: 0.809-0.933; P = 0.000). LPL activities decreased with the increased number of significantly stenosed vessels (P < 0.05).
Conclusions:
LPL activity and hs-CRP are significant predictors of premature stable CAD in male patients and are inversely correlated.
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