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Discriminative value of lipids and apoproteins in coronary heart disease

Atherosclerosis
|April 1, 1982
PubMed

Insights

The apolipoprotein B/A1 ratio and HDL-C levels effectively distinguish myocardial infarction survivors from healthy individuals. These lipid markers offer valuable insights for cardiovascular risk assessment.

Area of Science:

  • Cardiovascular Medicine
  • Biochemistry
  • Lipid Metabolism

Background:

  • Myocardial infarction (MI) survivors require accurate risk stratification for secondary prevention.
  • Traditional lipid profiles, including high-density lipoprotein cholesterol (HDL-C), are established cardiovascular risk factors.
  • The role of apolipoproteins in discriminating MI risk requires further elucidation.

Purpose of the Study:

  • To evaluate the discriminatory power of serum apolipoproteins and HDL-C in identifying male myocardial infarction survivors.
  • To compare the effectiveness of univariate and multivariate analyses using these biomarkers.

Main Methods:

  • Cross-sectional study involving 70 male MI survivors and 70 matched healthy controls.
  • Measurement of serum cholesterol, HDL-C, apolipoprotein A1 (Apo A1), apolipoprotein A2 (Apo A2), and apolipoprotein B (Apo B).
  • Univariate and multivariate logistic regression analyses were performed to assess discriminatory capacity.

Main Results:

  • The apolipoprotein B/Apo A1 ratio showed significant discriminatory power (72% exact classification) in univariate analysis.
  • Multivariate analysis revealed independent contributions of the Apo B/Apo A1 ratio, HDL-C, and Apo A2/Apo A1 ratio.
  • The combined markers achieved an 82% exact classification, with consistent performance across age subgroups.

Conclusions:

  • Apolipoprotein profiles, particularly the Apo B/Apo A1 ratio, provide valuable information complementary to HDL-C for discriminating MI survivors.
  • These findings support the utility of apolipoprotein determination in cardiovascular risk assessment.
  • Further prospective studies are warranted to confirm these results and their clinical implications.

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