Table 2.

Thrombotic risk according to the presence or absence of a PROS1 gene defect and other prothrombotic defects*

PROS1 gene abnormal (n = 57) PROS1 gene normal (n = 52)
Without other defect (n = 51) With other defect (n = 6) Without other defect (n = 45) With other defect (n = 7)
Male, n (%)  19 (37.2) 2 (33.3)  21 (46.6)  4 (57.2)  
No. (%) with thrombosis  21 (41.2)  2 (33.3) 3 (6.6)  1 (14.2)  
Total thrombotic events 41  3  4  1  
Years of follow-up  2381  288 1713  287  
Age at first thrombosis, median (range) 34.8 (17.1-69.5)  35.1  24.5 (20.4-35.7) 52.2  
Events per 1000 person-years, median (range)  17.2 (12.3-23.4)  10.4 (2.2-30.5) 2.3 (0.6-6.0)  3.4 (0.1-19.4)  
Relative risk for thrombosis (95% CI)  5.0 (1.5-16.8)  4.0 (0.7-23.7)  2.0 (0.2-19.1) 
PROS1 gene abnormal (n = 57) PROS1 gene normal (n = 52)
Without other defect (n = 51) With other defect (n = 6) Without other defect (n = 45) With other defect (n = 7)
Male, n (%)  19 (37.2) 2 (33.3)  21 (46.6)  4 (57.2)  
No. (%) with thrombosis  21 (41.2)  2 (33.3) 3 (6.6)  1 (14.2)  
Total thrombotic events 41  3  4  1  
Years of follow-up  2381  288 1713  287  
Age at first thrombosis, median (range) 34.8 (17.1-69.5)  35.1  24.5 (20.4-35.7) 52.2  
Events per 1000 person-years, median (range)  17.2 (12.3-23.4)  10.4 (2.2-30.5) 2.3 (0.6-6.0)  3.4 (0.1-19.4)  
Relative risk for thrombosis (95% CI)  5.0 (1.5-16.8)  4.0 (0.7-23.7)  2.0 (0.2-19.1) 
*

Other inherited prothrombotic defects include antithrombin deficiency, factor V Leiden, or prothrombin 20 210A allele.

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