Serum lipids, lipoproteins and apolipoproteins in black patients with angiographically defined coronary artery disease
Document Type
Article
Publication Date
1-1-1990
Abstract
The association between angiographically defined coronary artery disease (CAD) and serum lipids, lipoproteins, and apolipoproteins was evaluated in 151 black men and 245 black women. Patients with 70% or greater narrowing of at least one coronary artery or ≥50% stenosis of the left main coronary artery (n = 179) were compared to those with lesions of < 50% stenosis (n = 217) for total cholesterol (TC), low density lipoprotein-cholesterol (LDL-C), high density lipoprotein-cholesterol (HDL-C), LDL-C/HDL-C, triglycerides, apolipoprotein A-I, apolipoprotein B, and apolipoprotein A-I/B. A consistently more atherogenic pattern of lipids, lipoproteins, and apolipoproteins occurred only among the women. Using stepwise selection multiple logistic regression analysis, the ratio of apolipoprotein A-I/B (odds ratio= 0.38, 95% confidence limits 0.24-0.61) was the only statistically significant association of CAD in women, after adjusting for the effects of age, body mass index, and histories of smoking, hypercholesterolemia, hypertension, and diabetes. When stratified by median of total cholesterol, the ratio of apolipoprotein A-I/B was the most strongly associated with the presence of CAD in the lower half of the total cholesterol distribution ( < 208 mg/dl), whereas in the upper half of the total cholesterol distribution the total cholesterol/HDL-C ratio was more strongly associated with CAD. None of the variables studied was associated with CAD in men. These results support other studies suggesting that apolipoproteins may be better predictors of CAD. © 1990.
Publication Source (Journal or Book title)
Journal of Clinical Epidemiology
First Page
425
Last Page
432
Recommended Citation
Ford, E., Cooper, R., Simmons, B., & Castaner, A. (1990). Serum lipids, lipoproteins and apolipoproteins in black patients with angiographically defined coronary artery disease. Journal of Clinical Epidemiology, 43 (5), 425-432. https://doi.org/10.1016/0895-4356(90)90130-H