Table 4.
Parameters | TCZ group (n = 20) | TNFI group (n = 40) | p‐value* |
---|---|---|---|
Δ GI | −0.21 ± 0.19 | −0.11 ± 0.12 | 0.03 * |
Δ % sites with plaque | −4.2 ± 20.6 | −6.9 ± 16.5 | 0.81 |
Δ % sites with BOP | −6.3 ± 8.9 | −3.7 ± 9.3 | 0.32 |
Δ PD (mm) | −0.12 ± 0.17 | −0.14 ± 0.13 | 0.38 |
Δ % sites with PD ≥4 mm | −5.8 ± 13.4 | −0.1 ± 17.4 | 0.82 |
Δ CAL (mm) | −0.07 ± 0.14 | −0.02 ± 0.20 | 0.96 |
Δ % sites with CAL ≥4 mm | −2.9 ± 14.0 | +2.8 ± 17.4 | 0.90 |
RA, rheumatoid arthritis; GI, gingival index; BOP, bleeding on probing; PD, probing depth; CAL, clinical attachment level; TCZ, tocilizumab; TNFI, tumor necrosis factor inhibitor; n, number.
Values represent the mean ± standard deviation changes from baseline to 6 months after medication (−: decrease and +: increase), and the bold values show the statistical significance.
Significantly different between the groups, as assessed by Mann–Whitney U‐test (p < 0.05).