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

Acta Cardiologica
|July 15, 2009
PubMed

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.
Abstract

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