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Table 1 Baseline characteristics of patients with disease relapse (“relapsers”) or stable disease activity (“nonrelapsers”) during 1 year of follow-up

From: Calprotectin strongly and independently predicts relapse in rheumatoid arthritis and polyarticular psoriatic arthritis patients treated with tumor necrosis factor inhibitors: a 1-year prospective cohort study

Characteristic

Total (n = 95)

Nonrelapsers (n = 83)

Relapsers (n = 12)

p value

Age (years)

57 (50–66)

57 (50–66)

57 (48–63.5)

0.614

Female, n (%)

61 (64.2%)

53 (63.9%)

8 (66.7%)

1.000

Disease duration (years)

15 (9–21)

15 (9–21)

14.5 (7.5–24.5)

0.831

Diagnosis, n (%)

   

0.215

 Psoriatic arthritis

51 (53,7%)

47 (56.6%)

4 (33.3%)

 

 Rheumatoid arthritis

44 (46.3%)

36 (43,4%)

8 (66.7%)

 

Time to csDMARD (months)

25.6 (5.1–62.2)

24.4 (5.5–62.2)

32.6 (5.1–92.3)

0.911

Time to bDMARD (months)

98.5 (36.9–165.9)

98.5 (38.8–160.9)

95.9 (33.6225.9)

0.823

Time-to-remission/LDA (months)

3.27 (2.13–4.3)

3.07 (1.9–3.97)

20.4 (16.8–24.3)

< 0.001

Time-in-remission/LDA (months)

58.7 (26.7–86.6)

60.1 (27.6–88.0)

25.0 (9.4–59.3)

0.027

Calprotectin (μg/mL)

1.66 (0.69–2.68)

1.44 (0.62–2.34)

6.01 (5.01–6.44)

< 0.001

CRP (mg/dL)

0.10 (0.04–0.26)

0.09 (0.03–0.22)

0.17 (0.04–0.52)

0.388

ESR (mm)

10 (7–18)

10 (7–16)

14.5 (8–21.5)

0.225

Albumin (g/L)

42 (31–48)

43 (31–48)

31 (31–47)

0.210

Biologic treatment, n (%)

   

0.843

 Adalimumab

34 (35.8%)

30 (36.1%)

4 (33.3%)

 

 Etanercept

44 (46.3%)

39 (47.0%)

5 (41.7%)

 

 Infliximab

17 (17.9%)

14 (16.9%)

3 (25.0%)

 

Biological treatment duration (months)

61.6 (30.8–91.4)

63.2 (31.8–92.7)

39.9 (25.1–61.2)

0.136

Reduced dose of biologicsa, n (%)

45 (47.4%)

40 (48.2%)

5 (41.7%)

0.672

Monotherapy, n (%)

45 (47.4%)

42 (50.6%)

3 (25.0%)

0.127

Concomitant steroids, n (%)

18 (18.9%)

13 (15.7%)

5 (41.7%)

0.047

Global TNFi trough serum levels (μg/mL)

2.20 (1.07–6.26)

2.70 (1.18–6.83)

1.14 (0.73–1.52)

0.001

Adalimumab (μg/mL)

7.04 (2.69–9.40)

7.19 (5.78–9.88)

1.28 (0.73–1.59)

0.009

Etanercept (μg/mL)

1.45 (1.00–2.25)

1.52 (0.92–2.32)

1.24 (1.20–1.54)

0.698

Infliximab (μg/mL)

2.94 (0.86–3.26)

3.16 (1.92–4.84)

0 (0–1.05)

0.023

DAS28-ESR

2.03 (1.68–2.6)

1.99 (1.67–2.52)

2.43 (1.89–2.74)

0.145

Remission, n (%)

72 (75.8%)

65 (78.3%)

7 (58.3%)

0.175

Low disease activity, n (%)

23 (24.2%)

18 (21.7%)

5 (41.7%)

0.127

SDAI

6.03 (2.2–6.26)

6.02 (2.11–6.22)

6.18 (4.53–6.96)

0.087

CDAI

6 (2–6)

6 (2–6)

6 (4–6.5)

0.220

Global ultrasound score

8 (3–13)

8 (3–13)

17.5 (9.5–31)

0.041

PD score

1 (0–2)

1 (0–2)

5.5 (2.5–10)

< 0.001

SH score

7 (3–11)

6 (3–10)

8.5 (5–12)

0.210

PDUS, n (%)

50 (52.6%)

38 (45.8%)

8 (66.6%)

< 0.001

Number of joints with PDUS

1 (0–2)

1 (0–2)

3.5 (2.5–5)

< 0.001

UdAS, n (%)

29 (30.5%)

17 (20.5%)

7 (58.3%)

< 0.001

  1. Values are shown as median (interquartile range) unless otherwise stated
  2. Significant p values are shown in bold typeface
  3. bDMARD biologic disease-modifying antirheumatic drug, CDAI Clinical Disease Activity Index, CRP C-reactive protein, csDMARD conventional synthetic disease-modifying antirheumatic drug, DAS28 28-joint Disease Activity Score, ESR erythrocyte sedimentation rate, LDA low disease activity, PD power Doppler, PDUS power Doppler ultrasound synovitis, SH synovial hypertrophy, SDAI Simplified Disease Activity Index, TNFi tumor necrosis factor inhibitors, UdAS ultrasound-defined active synovitis
  4. aTreatment regimen with a lower amount of the drug or longer intervals of administration than those recommended in the package insert for each product