Laboratory values | RA | IRD (n = 56) | HI (n = 51) | Sensitivity (n = 50) | Specificity | PPV | NPV | AUC (ROC) (95%) CI |
---|
RF IgM (%) | 43 | 3 (6) | 4 (8) | 77 | 93 | 86 | 88 | 0.85 (0.79 to 0.91) |
RF IgA (%) | 47 | 8 (16) | 0 (0) | 84 | 92 | 85 | 91 | 0.88 (0.82 to 0.94) |
Anti-CCP2 (%) | 46 | 1 (2) | 1 (2) | 82 | 98 | 96 | 91 | 0.90 (0.85 to 0.96) |
Anti-CCP3 (%) | 43 | 4 (8) | 1 (2) | 77 | 95 | 90 | 88 | 0.86 (0.80 to 0.92) |
SE 1 or 2 copies (%) | 17 | 7 (14) | 5 (10) | 30 | 88 | 59 | 70 | 0.59 (0.52 to 0.66) |
- SE 1 copy (%) | 15 | 7 (14) | 5 (10) | 27 | 88 | 56 | 68 | 0.57 (0.51 to 0.64) |
- SE 2 copies (%) | 2 | 0 (0) | 0 (0) | 4 | 100 | 100 | 65 | 0.52 (0.49 to 0.54) |
- Anti-CCP, anti-cyclic citrullinated peptides; AUC, area under the curve in the ROC analysis; HI, healthy individuals; IRD, inflammatory rheumatic diseases; RA, rheumatoid arthritis; RF, rheumatoid factor; Sensitivity, the percentage of RA patients who would be identified as having RA by the laboratory tests (positive test results); Specificity, the percentage of control patients (IRD and HI together) who would be identified as not having RA by the laboratory tests (negative test results); PPV, positive predictive value or the proportion of RA patients with positive test results who are correctly diagnosed as having RA; NPV, negative predictive value or the proportion of control patients with negative test results who are correctly diagnosed as not having RA; SE, shared epitope