Cardiovascular Diseases Clinical Trial
Official title:
High Density Lipoprotein Subspecies and Coronary Disease
To investigate the relative contributions of high density lipoprotein-C (HDL-C) subspecies to risk for coronary heart disease (CHD) in two distinct existing populations (samples from the VA-HIT study and the Framingham Offspring Study [FOS]) as well as the response of these subfractions to gemfibrozil treatment.
BACKGROUND:
Coronary heart disease (CHD) continues to be a leading cause of death and disability in the
United States. Information about the contribution of different subspecies of HDL-C to
increased or decreased risk for premature CHD and the extent to which common lipoprotein
lipase (LPL) mutations affect HDL-C composition and subspecies could contribute to an
increased understanding of the role of HDL-C in determining CHD risk.
DESIGN NARRATIVE:
The following parameters will be measured in blood samples collected from the VA-HIT study
and the Framingham Offspring Study: apo A-I-containing HDL subspecies (prebeta, alpha, and
prealpha) in plasma using two-dimensional gel electrophoresis immunoblot and image analysis,
LpA-I and LpA-I/A-II in plasma using differential electroimmunoassay, and apo C-III in HDL
using immunoturbidometric assay. The study hypotheses are as follow. a) Subjects from the
placebo arm of VA-HIT will have significantly lower alpha l HDL subspecies, LpA-I, and apo
C-III in HDL, and higher HDL/alpha l and apo A-I/alpha l ratios than subjects free of
coronary heart disease from the Framingham Offspring Study. b) These parameters will also
predict prospectively risk of coronary heart disease in both groups. c) In the VA-HIT study,
treatment with gemfibrozil, which has been shown to be associated with a 22 percent
reduction in myocardial infarction and coronary heart disease death, will be associated with
increases in alpha l HDL subspecies, LpA-I, and apo C-III in HDL, as well as decreases in
HDL/alpha l and apo A-I/alpha l ratios, compared to placebo. d) The hypothesis that subjects
with specific mutations in the lipoprotein lipase gene have less beneficial changes in HDL
subspecies with gemfibrozil than subjects with no mutations will also be tested.
;
Observational Model: Case Control, Time Perspective: Cross-Sectional
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