Table 1. Crude OR and 95% CIs of the positive autoantibodies before and after treatment initiation among the studied groups of patients (A and B).
Follow-up | Patients with positive autoantibodies | ||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
aPL (ACL or anti-β2-GPI) | ACL IgG | ACL IgM | Anti-β2-GPI IgG | ANA | |||||||||||
n (%) | OR | 95% CIs | n (%) | OR | 95% CIs | n (%) | OR | 95% CIs | n (%) | OR | 95% CIs | n (%) | OR | 95% CIs | |
Group A: sodium valproate (n=30) | |||||||||||||||
Before treatment | 15 (50) | Baseline | 3 (10) | Baseline | 4 (13) | Baseline | 8 (24) | Baseline | 9 (30) | Baseline | |||||
6 m | 7 (23)* | 0.30* | 0.10–0.92* | 2 (7) | 0.64 | 0.10–4.15 | 0 (0) | - | - | 5 (17) | 0.55 | 0.16–1.93 | 5 (17) | 0.47 | 0.14–1.61 |
12 m | 11 (36) | 0.58 | 0.21–1.62 | 2 (7) | 0.64 | 0.10–4.15 | 2 (7) | 0.46 | 0.08–2.75 | 7 (23) | 0.84 | 0.26–2.70 | 6 (20) | 0.58 | 0.18–1.91 |
24 m | 13 (43) | 0.76 | 0.28–2.11 | 3 (10) | 1.00 | 0.19–5.40 | 3 (10) | 0.72 | 0.15–3.54 | 7 (23) | 0.84 | 0.26–2.70 | 9 (30) | 1.00 | 0.33–3.02 |
Group B: carbamazepine (n=20) | |||||||||||||||
Before treatment | 7 (35) | Baseline | 1 (5) | Baseline | 3 (15) | Baseline | 3 (15) | Baseline | 3 (15) | Baseline | |||||
6 m | 5 (25) | 0.62 | 0.16–2.43 | 0 (0) | - | - | 2 (10) | 0.63 | 0.09–4.24 | 3 (15) | 1.00 | 0.18–5.67 | 1 (5) | 0.30 | 0.03–3.15 |
12 m | 9 (45) | 1.52 | 0.43–5.43 | 1 (5) | 1.00 | 0.06–17.18 | 4 (20) | 1.42 | 0.27–7.34 | 4 (20) | 1.42 | 0.27–7.34 | 1 (5) | 0.30 | 0.03–3.15 |
24 m | 8 (40) | 1.24 | 0.34–4.46 | 0 (0) | - | - | 4 (20) | 1.42 | 0.27–7.34 | 4 (20) | 1.42 | 0.27–7.34 | 1 (5) | 0.30 | 0.03–3.15 |
*Statistically significant associations.
ACL: anticardiolipin antibodies, ANA: antinuclear antibodies, anti-β2-GPI: anti-β2-glycoprotein I antibodies, aPL: antiphospholipid antibodies, CI: confidence interval, Ig: immunoglobulin, m: months, OR: odds ratios.