Cardiovascular Diseases Clinical Trial
To investigate hemostatic variables in relation to cardiovascular risk in the Framingham Offspring Study cohort.
BACKGROUND:
Elevation of platelet reactivity plasminogen activator inhibitor, fibrinogen, von
Willebrand's factor, and factor VII have been reported to increase myocardial infarction
risk. Myocardial infarction and sudden cardiac death are more frequent in the morning when
platelet activity is increased and fibrinolysis is decreased. Reduction of recurrent
myocardial infarction by aspirin and coumadin suggests causal roles for platelet activity
and coagulation. Increases in viscosity and decreases in anti-thrombin III and Protein C
have been linked with increased thrombosis. Despite these findings, a coherent picture of
these disparate hemostatic indices as cardiac risk factors has yet to emerge.
DESIGN NARRATIVE:
Platelet reactivty, plasminogen activatator inhibitor, fibrinogen, von Willebrand's factor,
factor VII, and other hemostatic risk factors were measured in all 4,000 subjects of the
Framingham Offspring Study. The data were combined with the regularly collected Framingham
data to: determine the relationships between hemostatic factors and carotid atherosclerosis
as assessed by ultrasound; determine the relationship between hemostatic factors and the
traditional cardiac risk factors; and determine if hemostatic risk factors independently
predict myocardial infarction and cardiac death.
The study completion date listed in this record was obtained from the "End Date" entered in
the Protocol Registration and Results System (PRS) record.
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