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. 2018 Oct 14;194(3):391–399. doi: 10.1111/cei.13206

Table 1.

Baseline patient characteristics (n = 231) and treatment regimen started at the inclusion visit

Women, n (%) 162 (70·1)
Mean age (years ± s.d.) 57·4 ± 13·0
Rheumatoid factor‐positive, n (%) 150 (64·9)
IgG anti‐CCP‐positive, n (%) 172 (74·4)
DAS28 (mean ± s.d.)a 5·1 ± 1·2
HAQ (mean ± s.d.)b 1·0 ± 0·6
Mean IgG anti‐CCP level (U/ml ± s.e.m.)c 180·2 ± 9·7
Mean IgA anti‐CCP level (µg/ml ± s.e.m.)d 7·5 ± 0·9
Mean IgM anti‐CCP level (AU/ml ± s.e.m.)e 9950·2 ± 1262
Mean SIgA anti‐CCP level (AU/ml ± s.e.m.)f 3929·4 ± 389·7
Oral corticosteroids, n (%)h 138 (59·7)
csDMARD single therapy, n (%) 196 (84·8)
csDMARD combination therapy, n (%) 20 (8·7)
bDMARD therapy, n (%) 1 (0·4)

DAS28 = disease activity score 28; HAQ = health assessment questionnaire; csDMARD = conventional synthetic disease‐modifying anti‐rheumatic drug (single therapy including methotrexate (MTX), salazopyrin (SSZ), anti‐malaria or leflunomide. Combination therapy including different combinations of MTX, SSZ, anti‐malarial and imurel) and bDMARD = biological disease‐modifying anti‐rheumatic drug; s.e.m. = standard error of the mean.

a

Data available from 215 patients;

b

data available from 206 patients;

c

cut‐off: ACPA IgG 7U/ml;

d

anti‐citrullinated protein antibodies (ACPA) immunoglobulin (Ig)A 2 µg/l;

e

ACPA IgM 6032 AU/ml;

f

ACPA SIgA 3089 AU/ml;

data available from 230 patients.