Key result
Factor V Leiden prevalence was significantly higher in patients with DVT (33.3%) than in patients with PTE (12.5%), with no significant difference between DVT alone and combined DVT/PTE.
Why the study?
Does the prevalence of factor V Leiden and prothrombin 20210 A mutation differ between patients with DVT, PTE, and combined DVT/PTE?
Case-Control (n=228)
Does the prevalence of factor V Leiden and prothrombin 20210 A mutation differ between patients with DVT, PTE, and combined DVT/PTE?
Factor V Leiden is significantly more frequent in patients with DVT than in those with isolated PTE, but patients with DVT who carry the mutation are not at lower risk for pulmonary embolism.
Factor V Leiden was associated with DVT over isolated PTE; hypothesis-generating for differential embolism risk in carriers.
Factor V Leiden mutation and prothrombin variant 20210 A are well-known risk factors for venous thrombosis (DVT). Recent papers have reported a lower prevalence of factor V Leiden in patients with pulmonary thromboembolism (PTE) than in patients with deep venous thrombosis. The aim of the present study was to compare the prevalence of factor V Leiden and the prothrombin 20210 G <-- A mutation in patients with DVT and in patients with PTE. We studied 128 consecutive patients (45 with DVT, 40 with PTE, and 43 with DVT and PTE) for factor V Leiden and prothrombin 20210 A. One hundred healthy persons matched by age and sex were used as controls. Factor V Leiden was present in five of the patients with PTE [12.5%; 95% confidence interval (CI), 1.5-23.5%; not significant], 15 of the patients with DVT (33.3%; 95% CI, 9.6-38.7%; P < 0.001), and 12 of the patients with DVT and PTE (27.9%; 95% CI, 4.8-33%; P = 0.001). Results for the prothrombin 20210 A mutation were as follows: four of 40 patients with PTE (10%; 95% CI, 0-13.3%; P = 0.46), nine of 45 (20%) of the patients with DVT (95% CI, 0.5-25.5%; P < 0.05) and eight of 43 with DVT and PTE were heterozygous (18.6%; 95% CI, 0-23.9%; P = 0.02). In conclusion, there is a significantly higher frequency of factor V Leiden among patients with DVT than in patients with PTE. However, there is no significant difference of factor V Leiden or 20210 A prothrombin mutation in patients with DVT than in patients with combined DVT/PTE, therefore patients with DVT, carriers of the mutations, do not appear to be at lower risk for pulmonary embolism.
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Boyanovsky et al. (2001) conducted a case-control in Pulmonary thromboembolism and deep venous thrombosis (n=228). Factor V Leiden and prothrombin 20210 A variant vs. Healthy controls and cross-group comparisons was evaluated on Prevalence of factor V Leiden and prothrombin 20210 A mutation. Factor V Leiden prevalence was significantly higher in patients with DVT (33.3%) than in patients with PTE (12.5%), with no significant difference between DVT alone and combined DVT/PTE.
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