The major goal of this project is to determine the extent to which changes in plasma levels of specific lipoproteins, lipoprotein subspecies, and apolipoproteins are associated with quantitative changes in coronary atherosclerosis during the course of a controlled three year coronary risk factor intervention program.
A second aim i s to identify those lipoprotein variables that are related at baseline to extent of coronary atherosclerosis before initiation of treatment. Lipoprotein analyses will be carried out in 300 patients admitted to Stanford University Medical Center for management of coronary artery disease (coronary artery bypass surgery, transluminal percutaneous coronary angioplasty, or medical treatment). Initial lipoprotein analyses will be performed three weeks after surgery and after medical stabilization (1-3 weeks) in other patients. Subfractions of plasma very low density, low density, and high density lipoproteins (VLDL, LDL, HDL) will be measured by analytic ultracentrifugation with a computer-based quantitation procedure. LDL and HDL subspecies will also be measured by high-resolution polyacrylamide gradient gel electrophoresis. Apolipoproteins AI, AII and B will be measured by enzyme-linked immunosorption assay. Coronary angiography will be performed and computerized quantitation of non-bypassed or non-dilated coronary artery segments will be carried out as part of an existing protocol at Stanford University before initial treatment and at three years following medical management (all subjects) and intensive multiple risk factor intervention (one-half of the subjects, randomly assigned). The special intervention program at Stanford includes improved nutrition, weight reduction, increased aerobic exercise, stress management, and individualized treatment including elimination of cigarette use, reduction of hypertension, and LDL reduction. Lipoprotein studies will be repeated after one, two and three years of follow-up in all subjects. Analyses of lipid and lipoprotein measurements in relation to changes in coronary atherosclerosis will make it possible to identify those lipoprotein parameters most closely involved in this disease process. The results will also indicate whether detailed measurements of specific lipoprotein subclasses and apolipoproteins are more informative than conventional lipid measurements in predicting the extent of coronary artery disease, and in assessing the effects of strategies directed at its prevention and treatment.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL033577-03
Application #
3345594
Study Section
Clinical Trials Review Committee (CLTR)
Project Start
1984-12-01
Project End
1988-11-30
Budget Start
1986-12-01
Budget End
1987-11-30
Support Year
3
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Lawrence Berkeley National Laboratory
Department
Type
Organized Research Units
DUNS #
078576738
City
Berkeley
State
CA
Country
United States
Zip Code
94720
Badzioch, Michael D; Igo Jr, Robert P; Gagnon, France et al. (2004) Low-density lipoprotein particle size loci in familial combined hyperlipidemia: evidence for multiple loci from a genome scan. Arterioscler Thromb Vasc Biol 24:1942-50
Paganini-Hill, A; Dworsky, R; Krauss, R M (1996) Hormone replacement therapy, hormone levels, and lipoprotein cholesterol concentrations in elderly women. Am J Obstet Gynecol 174:897-902
Miller, B D; Alderman, E L; Haskell, W L et al. (1996) Predominance of dense low-density lipoprotein particles predicts angiographic benefit of therapy in the Stanford Coronary Risk Intervention Project. Circulation 94:2146-53
Campos, H; Roederer, G O; Lussier-Cacan, S et al. (1995) Predominance of large LDL and reduced HDL2 cholesterol in normolipidemic men with coronary artery disease. Arterioscler Thromb Vasc Biol 15:1043-8
Superko, H R; Myll, J; DiRicco, C et al. (1994) Effects of cessation of caffeinated-coffee consumption on ambulatory and resting blood pressure in men. Am J Cardiol 73:780-4
Tribble, D L; Krauss, R M (1993) HDL and coronary artery disease. Adv Intern Med 38:1-29
Superko, H R; Haskell, W L; Krauss, R M (1993) Association of lipoprotein subclass distribution with use of selective and non-selective beta-blocker medications in patients with coronary heart disease. Atherosclerosis 101:1-8
Vega, G L; Grundy, S M (1992) Occurrence of species of low-density lipoprotein with defective clearance in patients with primary moderate hypercholesterolaemia. J Intern Med 232:405-13
Vega, G L; Krauss, R M; Grundy, S M (1990) Pravastatin therapy in primary moderate hypercholesterolaemia: changes in metabolism of apolipoprotein B-containing lipoproteins. J Intern Med 227:81-94
Williams, P T; Krauss, R M; Vranizan, K M et al. (1989) Effects of exercise-induced weight loss on low density lipoprotein subfractions in healthy men. Arteriosclerosis 9:623-32

Showing the most recent 10 out of 13 publications