General data of the participants in the developmental and clinical validation cohorts
. | Developmental cohorts . | Clinical 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 cohorts . | Clinical 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) |