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Updated: Jun 4, 2026

Measurement of Factor V Activity in Human Plasma Using a Microplate Coagulation Assay
Published on: September 9, 2012
Factor V Leiden mutation and the risks for thromboembolic disease: a clinical perspective
1Brigham and Women's Hospital, Boston, Massachusetts, USA.
Factor V Leiden mutation increases venous thromboembolism risk but screening utility is uncertain. Further trials are needed to determine optimal anticoagulation strategies for affected individuals.
Area of Science:
- Genetics
- Hematology
- Thrombosis Research
Background:
- Factor V Leiden is a common genetic mutation causing resistance to activated protein C.
- This resistance leads to a hypercoagulable state and increased risk of blood clots.
- The mutation is present in 4-6% of the U.S. population.
Purpose of the Study:
- To review clinical data on factor V Leiden mutation.
- Emphasis on prevalence and risks of thromboembolism.
- Implications for screening and management strategies.
Main Methods:
- MEDLINE search (1993-April 1997) and bibliography review.
- Inclusion of case-control, cohort studies, and original research articles.
- Review of case reports when analytic data were unavailable.
Main Results:
- Factor V Leiden mutation increases venous thromboembolism risk 3-6 fold, especially without transient risk factors.
- Risk is higher with coexisting thrombotic predispositions (e.g., oral contraceptives, deficiencies).
- No increased risk for arterial thrombosis observed; anticoagulation benefit is unknown.
Conclusions:
- Factor V Leiden mutation predisposes to venous thromboembolism.
- Screening utility remains uncertain.
- Management decisions depend on trials evaluating anticoagulation benefits versus risks.
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