Clinical Utility of Different Lipid Measures for Prediction of Coronary Heart Disease in Men and Women.
From: Framingham Heart Study, 73 Mount Wayte Ave, Suite 2, Framingham, MA 01702-5803. vasan@bu.edu.
JAMA : the journal of the American Medical Association
- Publish Date: Aug 2007
- ISSN: 1538-3598
- Volume: 298
- Issue: 7
- Pages: 776-85
- Medium: Internet
- Language: English
- Citation (JAMA): Ingelsson Erik, Schaefer Ernst J, Contois John H, et al. Clinical Utility of Different Lipid Measures for Prediction of Coronary Heart Disease in Men and Women.. JAMA Aug 2007;298:776-85
Abstract
CONTEXT: Evidence is conflicting regarding the performance of apolipoproteins vs traditional lipids for predicting coronary heart disease (CHD) risk. OBJECTIVES: To compare performance of different lipid measures for CHD prediction using discrimination and calibration characteristics and reclassification of risk categories; to assess incremental utility of apolipoproteins over traditional lipids for CHD prediction. DESIGN, SETTING, AND PARTICIPANTS: Population-based, prospective cohort from, Framingham, Massachusetts. We evaluated serum total cholesterol, high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), non-HDL-C, apolipoprotein (apo) A-I and apo B, and 3 lipid ratios (total cholesterol:HDL-C, LDL-C:HDL-C, and apo B:apo A-I) in 3322 middle-aged white participants who attended the fourth offspring examination cycle (1987-1991) and were without cardiovascular disease. Fifty-three percent of the participants were women. MAIN OUTCOME MEASURE: Incidence of first CHD event (recognized or unrecognized myocardial infarction, angina pectoris, coronary insufficiency, or coronary heart disease death). RESULTS: After a median follow-up of 15.0 years, 291 participants, 198 of whom were men, developed CHD. In multivariate models adjusting for nonlipid risk factors, the apo B:apo A-I ratio predicted CHD (hazard ratio [HR] per SD increment, 1.39; 95% confidence interval [CI], 1.23-1.58 in men and HR, 1.40; 95% CI, 1.16-1.67 in women), but risk ratios were similar for total cholesterol:HDL-C (HR, 1.39; 95% CI, 1.22-1.58 in men and HR, 1.39; 95% CI, 1.17-1.66 in women) and for LDL-C:HDL-C (HR, 1.35; 95% CI, 1.18-1.54 in men and HR, 1.36; 95% CI 1.14-1.63 in women). In both sexes, models using the apo B:apo A-I ratio demonstrated performance characteristics comparable with but not better than that for other lipid ratios. The apo B:apo A-I ratio did not predict CHD risk in a model containing all components of the Framingham risk score including total cholesterol:HDL-C (P = .12 in men; P = .58 in women). CONCLUSIONS: In this large, population-based cohort, the overall performance of apo B:apo A-I ratio for prediction of CHD was comparable with that of traditional lipid ratios but did not offer incremental utility over total cholesterol:HDL-C. These data do not support measurement of apo B or apo A-I in clinical practice when total cholesterol and HDL-C measurements are available.
Mesh Headings (Keywords): Apolipoprotein A-I, Apolipoproteins, Apolipoproteins B, Cholesterol, HDL, Cholesterol, LDL, Coronary Disease, Female, Humans, Likelihood Functions, Lipids, Male, Middle Aged, Proportional Hazards Models, Prospective Studies, Risk Factors
Check for Full Text / PubMed Unique Identifier (PMID): 17699011
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