Cardiovascular Diseases Clinical Trial
To assess the interaction between hormone replacement therapy and the prothrombotic mutations, Factor V Leiden and the recently described prothrombin mutation (20210A) on the incidence of venous thromboembolism (VTE) in a population-based case-control study conducted at Group Health Cooperative of Puget Sound (GHC).
BACKGROUND:
Epidemiologic studies have identified Factor V Leiden as the most common cause of heritable
thrombophilia, a prothrombotic mutation associated with a 5 to 7-fold increase in the risk
of venous thromboembolism (VTE). In pre-menopausal women, the use of oral contraceptives is
associated with a 4-fold increase in VTE risk, and the joint effects of oral contraceptive
use and Factor V Leiden carriership increase the VTE risk of by a factor of 35. Recently,
the results of several observational studies and randomized clinical trials suggest that in
post-menopausal women, the use of hormone replacement therapy is associated with a 3-fold
increase in VTE risk. Whether post-menopausal women with prothrombotic mutations experience
a similar 20-fold increase in risk when they take post-menopausal hormones remains unknown.
DESIGN NARRATIVE:
In this case-control study, post-menopausal women with a first episode of objectively
confirmed venous thromboembolism, and population-based controls were identified and
recruited from the GHC enrollment files. Controls were frequency matched to the cases on age
and calendar-year. Data collection included a review of ambulatory medical record and a
telephone interview. The GHC computerized pharmacy database was used to assess exposure to
hormone replacement therapy. A venous blood specimen was obtained from consenting subjects,
processed into aliquots of white cells, plasma, and red cells, and stored at 70 degrees C
prior to laboratory analysis. DNA was extracted from white cells, and molecular genotyping
assays were conducted to assess carriership of prothrombotic mutations.
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