Table 2.
ACPA subtype* |
Pre-clinical RA Cases (n=255) |
Matched Controls (n=778) |
p value |
---|---|---|---|
Biglycan | 12 (4.7%) | 7 (0.9%) | <0.001 |
Clusterin | 26 (10.2%) | 13 (1.7%) | <0.001 |
Enolase | 6 (2.4%) | 4 (0.5%) | 0.02 |
Fibrinogen | 45 (17.7%) | 34 (4.4%) | <0.001 |
Histone 2A | 14 (5.5%) | 11 (1.4%) | 0.001 |
Histone 2B | 22 (8.6%) | 13 (1.7%) | <0.001 |
Vimentin | 38 (14.9%) | 16 (2.1%) | <0.001 |
| |||
≥1 ACPA | 59 (23.1%) | 59 (7.6%) | <0.001 |
≥2 ACPAs | 40 (15.7%) | 16 (2.1%) | <0.001 |
P values are from univariable conditional logistic regression models.
For each ACPA subtype, antibodies against the following number of epitopes were tested. Subjects testing positive for antibody against one or more epitope were considered positive for that ACPA subtype: biglycan (1), clusterin (2), enolase (1), fibrinogen (5), histone 2A (2), histone 2B (2), vimentin (2)