Table 1.

General data of the participants in the developmental and clinical validation cohorts

Developmental cohortsClinical validation cohorts
Patients with APS (n = 48)Controls (n = 64)Patients with APS (n = 33)Controls (n = 62)Thrombosis controls (n = 38)
Age, mean ± SD, y 46 ± 14 67 ± 11  47 ± 12 69 ± 11  47 ± 13  
Sex, n (% male) 18 (38) 47 (73)  9 (27) 51 (82)  16 (42)  
Primary APS, n (%) 30 (62)  33 (100)   
Secondary APS, n (%) 18 (38)  0 (0)   
LA, n (%) 39 (81)  29 (88)  0 (0) 
Anti-CL antibodies, n (%) 38 (79)  25 (76)  0 (0) 
Anti–β2-GPI antibodies, n (%) 27 (56)  34 (81)  0 (0) 
Thrombosis, n (%) 48 (100) 4 (6%)  31 (94) 7 (11)  38 (100)  
Pregnancy morbidity, n (%) 8 (17)  4 (12)  0 (0) 
INR
(treatment range21,26,27
NA
(2.0-3.0) 
2.8 ± 0.8
(2.0-3.0) 
2.5 ± 0.9
(2.0-3.0) 
3.1 ± 1.0
(2.0-3.0) 
2.1 ± 0.3 (VKA)
1.1 ± 0.3 (non-VKA)
(2.0-3.0) 
Developmental cohortsClinical validation cohorts
Patients with APS (n = 48)Controls (n = 64)Patients with APS (n = 33)Controls (n = 62)Thrombosis controls (n = 38)
Age, mean ± SD, y 46 ± 14 67 ± 11  47 ± 12 69 ± 11  47 ± 13  
Sex, n (% male) 18 (38) 47 (73)  9 (27) 51 (82)  16 (42)  
Primary APS, n (%) 30 (62)  33 (100)   
Secondary APS, n (%) 18 (38)  0 (0)   
LA, n (%) 39 (81)  29 (88)  0 (0) 
Anti-CL antibodies, n (%) 38 (79)  25 (76)  0 (0) 
Anti–β2-GPI antibodies, n (%) 27 (56)  34 (81)  0 (0) 
Thrombosis, n (%) 48 (100) 4 (6%)  31 (94) 7 (11)  38 (100)  
Pregnancy morbidity, n (%) 8 (17)  4 (12)  0 (0) 
INR
(treatment range21,26,27
NA
(2.0-3.0) 
2.8 ± 0.8
(2.0-3.0) 
2.5 ± 0.9
(2.0-3.0) 
3.1 ± 1.0
(2.0-3.0) 
2.1 ± 0.3 (VKA)
1.1 ± 0.3 (non-VKA)
(2.0-3.0) 

INR, International normalized ratio; NA, not available; SD, standard deviation.

P < .001 compared with patients with APS.

No significant difference compared with APS patients.

INR data were not available for all participants; results for a subset of the cohorts is shown.

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