Cardiovascular Diseases Clinical Trial
To determine the effect of the method of hyperglycemic management on pro- thrombotic potential in diabetic subjects.
BACKGROUND:
Cardiovascular disease is the leading cause of death in patients with diabetes. The BARI 2D
study is designed to determine the potential value of specific treatment regimens for those
with diabetes and will test the hypothesis that "with a target HbA1C of less than 7.5%, a
strategy of hyperglycemic management directed at insulin sensitization results in lower 5
year mortality compared to a strategy of insulin provision." This ancillary study is
designed to provide mechanistic insight into potential benefits derived from two different
treatment strategies employed by characterizing the thrombotic potential in those patients
assigned to the aggressive medical management strategy and long-range goal is to demonstrate
that treatment of diabetes with regimens that reduce thrombotic potential decreases
cardiovascular risk. The results of this ancillary study should help to define the extent to
which specific regimens diminish the pro-thrombotic state.
The study is in response to an initiative on Ancillary Studies in Heart, Lung, and Blood
Disease Trials released in June, 2000.
DESIGN NARRATIVE:
Thrombotic potential will be assessed by determination of both platelet reactivity and
thrombin generation and activity. Preliminary studies have found that patients with diabetes
have increased coronary intervention. Further, thrombin generation and activity is increased
in diabetic subjects. Preliminary evidence suggests that treatment with an
insulin-sensitizing regimen reduces platelet reactivity, thrombin generation and thrombin
activity. The BARI 2D study is ideally suited for determination of the effect of the method
of glycemic control on pro-thrombotic potential. In aim 1 the investigators will determine
platelet reactivity before and during the first year of treatment in patients randomized to
medical treatment and randomized also to either an insulin-sensitizing regimen or an
insulin-providing regimen. They will use a flow cytometry-based assay of platelet function
that they have developed and validated. In aim 2 they will determine the effect of treatment
on thrombin generation and activity in the same group of patients. Thrombin generation will
be determined by measuring the concentration in blood of a cleavage fragment (prothrombin
fragment 1+2). Thrombin activity will be determined by measuring the concentration in blood
of a second cleavage fragment (fibrinopeptide A). The results of the studies will determine
the effect of the method of hyperglycemic management on pro-thrombotic potential. Further,
these results will define the importance of prothrombotic potential in diabetic subjects
while potentially identifying new therapeutic targets in patients with diabetes and other
insulin resistant states.
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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