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. 2015 Jun 6;17(1):151. doi: 10.1186/s13075-015-0663-9

Table 1.

Demographic, disease and treatment characteristics of 201 patients at inclusion and comparison between groups according to baseline pneumococcal serology

Characteristics All (N = 201) Vaccination groupa (n = 60) Observation groupb (n = 141) p-Value
Median age (IQR), yr 53.9 (43.3–65.7) 58.6 (37.0–71.9) 53.1 (42.6–61.9) NS
Male/female, n 84/117 22/38 62/79 NS
Disease type
 Psoriasis, n (%) 52 (26) 8 (13) 44 (31) 0.03
 Rheumatoid arthritis, n (%) 41 (20) 13 (22) 28 (20) NS
 Spondylarthropathies, n (%) 15 (7) 4 (7) 11 (8) NS
 Connective tissue diseases, n (%) 31 (15)c 11 (18) 20 (14) NS
 Systemic vasculitis, n (%) 24 (12)d 12 (20) 12 (9) 0.03
 Miscellaneous inflammatory conditions, n (%) 38 (19)e 12 (20) 26 (18) NS
Disease activity according to PGA 0.019
 Inactive, n (%) 28 (14) 2 (3) 26 (18)
 Moderately active, n (%) 120 (60) 44 (73) 76 (54)
 Active, n (%) 44 (22) 12 (20) 32 (23)
 Very active, n (%) 9 (5) 2 (3) 7 (5)
Treatment
 Systemic corticosteroids, n (%) 91 (45) 41 (68) 50 (36) <0.001
 Daily prednisone dose, median (IQR), mg 10 (5–30) 10 (5–30) 10 (7.5–27.5) NS
 Prednisone ≥20 mg/day, n (%) 35 (17) 16 (27) 19 (14) 0.02
 Immunosuppressant, n (%) 181 (90)f 50 (83) 131 (93) NS
 Other DMARDs, n (%) 25 (12)g 10 (17) 15 (11) NS
 Previous rituximab treatment, n (%) 17 (9) 5 (8) 12 (9) NS
 Treatment duration, median (IQR), yr 2 (0–6) 2 (0–6) 2 (0–6) NS
Total serum IgG, median (IQR), g/L 10.8 (8.6–13.2) 9.0 (7.5–12.1) 11.2 (9–13.4) 0.003
Total serum IgA, median (IQR), g/L 2.1 (1.6–3.1) 2.1 (1.3–3.0) 2.3 (1.6–3.2) NS
Total serum IgM, median (IQR), g/L 0.9 (0.7–1.4) 0.8 (0.6–1.2) 1.0 (0.7–1.4) NS

Abbreviations: DMARD disease-modifying anti-rheumatic drug, Ig immunoglobulin, IQR interquartile range, NS not significant, PGA Physician Global Assessment. p-Values were obtained by χ 2 and Mann–Whitney U tests

aIgG ≥0.5 μg/ml for fewer than four of six serotypes

bIgG ≥0.5 μg/ml for four or more of six serotypes

cSystemic lupus erythematosus (n = 13), dermatomyositis (n = 5), mixed connective tissue disease (n = 4), polymyositis (n = 3), anti-synthetase syndrome (n = 3), undifferentiated connective tissue disease (n = 2), systemic sclerosis (n = 1)

dGiant cell arteritis (n = 7), granulomatosis with polyangiitis (n = 6), primary angiitis of the central nervous system (n = 5), microscopic polyangiitis (n = 4), Takayasu arteritis (n = 1), polyarteritis nodosa (n = 1)

ePemphigus vulgaris (n = 7), adult-onset Still disease (n = 6), bullous pemphigoid (n = 5), Behçet disease (n = 4), orbital pseudotumor (n = 3), unspecified inflammatory disorders (n = 3), autoinflammatory disorders (n = 2), cicatricial pemphigoid (n = 2), uveitis (n = 2), retroperitoneal fibrosis (n = 2), polymyalgia rheumatica (n = 1), aortitis (n = 1)

fMethotrexate (n = 60), adalimumab (n = 24), infliximab (n = 24), azathioprine (n = 23), mycophenolate mofetil (n = 22), mycophenolic acid (n = 3), tocilizumab (n = 19), leflunomide (n = 11), etanercept (n = 7), ustekinumab (n = 7), golimumab (n = 4), cyclophosphamide (n = 2), anakinra (n = 2), abatacept (n = 2), rituximab in the preceding 6 months (n = 2), chlorambucil (n = 1), ciclosporin A (n = 1), tacrolimus (n = 1), certolizumab (n = 1). More than one immunosuppressive agent was used in 37 patients (18 %)

gHydroxychloroquine (n = 16), sulfasalazine (n = 7), colchicine (n = 2), dapsone (n = 2). More than one non-immunosuppressive DMARD was used in two patients