Table 1 Patient demographics and baseline clinical features.

From: Prediction of disease flare by biomarkers after discontinuing biologics in patients with rheumatoid arthritis achieving stringent remission

 

Total, n = 36

Flare ( +), n = 20

Flare (−), n = 14

p-value

Female, n (%)

29 (80.6)

16 (80.0)

12 (85.7)

1.00b

Age (years)

69 (53–75)

69 (48–76)

69 (54–75)

0.90a

Height (cm)

156 (152–160)

156 (152–160)

159 (154–160)

0.25a

Weight (kg)

50 (48–57)

50 (45–57)

51 (50–57)

0.32a

RA duration (years)

5.2 (2.3–9.8)

5.7 (2.5–9.8)

4.1 (1.6–9.7)

0.46a

RA onset to bDMARDs (years)

1.3 (0.4–7.8)

2.6 (0.5–7.1)

0.6 (0.4–5.7)

0.24a

bDMARD continuation (years)

2.1 (1.4–3.5)

1.9 (1.5–2.8)

2.7 (0.9–3.6)

0.83a

Remission duration (months)

20 (9–31)

18 (10–26)

24 (9–37)

0.42a

Failed bDMARDs, n (%)

0

26 (72.2)

14 (70.0)

10 (71.4)

 

1

8 (22.2)

5 (25.0)

3 (21.4)

0.95b

2

2 (5.6)

1 (5.0)

1 (7.1)

 

Radiographic stage I or II, n (%)

27 (75.0)

17 (85.0)

10 (71.4)

0.41b

Anti-CCP positive, n (%)

26 (76.5)

16 (84.2)

8 (61.5)

0.22b

Rheumatoid factor positive, n (%)

28 (77.8)

17 (85.0)

9 (64.3)

0.23b

Rheumatoid factor titre (IU/mL)

43.6 (15.4–110.4)

59.7 (16.2–115.1)

24.4 (6.8–62.5)

0.18a

Tender joint count of 28 joints

0 (0–0)

0 (0–0)

0 (0–0)

1.00a

Swollen joint count of 28 joints

0 (0–0)

0 (0–1)

0 (0–0)

0.19a

Patient global assessment (/100)

3 (0–6)

3 (0–8)

3 (1–6)

0.76a

Physician global assessment (/100)

0 (0–3)

1 (0–5)

0 (0–2)

0.30a

HAQ-DI

0 (0–0)

0 (0–0)

0 (0–0.2)

0.71a

CRP (mg/dL)

0.04 (0.01–0.09)

0.04 (0.01–0.1)

0.04 (0.02–0.06)

0.83a

ESR (mm/ 1 h)

16 (6–27)

20 (8–35)

9 (5–18)

0.077a

Matrix metalloproteinase-3 (ng/mL)

53.8 (22.6–89.3)

57.1 (45.2–137.9)

50.5 (44.4–68.0)

0.24a

DAS28-ESR

2.0 (1.3–2.4)

2.3 (1.4–2.8)

1.6 (1.1–2.1)

0.058a

SDAI

0.4 (0.2–1.5)

0.6 (0.3–2.1)

0.4 (0.1–1.2)

0.45a

ACR/EULAR Boolean remission, n (%)

31 (86.1)

17 (85.0)

12 (85.7)

1.00b

Ultrasound grey-scale

7 (1–10)

6 (1–12)

8 (3–10)

0.54a

Ultrasound Power Doppler

0 (0–1)

0 (0–1)

0 (0–1)

0.88a

Ultrasound total score

7 (1–12)

6 (1–13)

8 (3–11)

0.53a

Discontinued bDMARDs

TNF inhibitors, n (%)

26 (72.2)

14 (70.0)

12 (85.7)

0.42b

Adalimumab

3 (8.3)

3 (15.0)

0 (0.0)

 

Certolizumab pegol

2 (5.6)

0 (0.0)

2 (14.3)

 

Etanercept

10 (27.8)

5 (25.0)

5 (35.7)

 

Golimumab

5 (13.9)

2 (10.0)

3 (21.4)

 

Infliximab

6 (16.7)

4 (20.0)

2 (14.3)

 

Non-TNF inhibitors, n (%)

    

Abatacept

4 (11.1)

3 (15.0)

1 (7.1)

 

Tocilizumab

6 (16.7)

3 (15.0)

1 (7.1)

 

Concomitant csDMARDs, n (%)

Methotrexate

25 (69.4)

12 (60.0)

11 (78.6)

0.29b

Methotrexate dose (mg/week in users)

8 (7–10)

9 (7–10)

8 (8–10)

0.95b

Salazosulfapyridine

13 (36.1)

8 (40.0)

5 (35.7)

1.00b

Bucillamine

1 (2.8)

1 (5.0)

0 (0.0)

1.00b

Iguratimod

1 (2.8)

1 (5.0)

0 (0.0)

1.00b

Leflunomide

1 (2.8)

1 (5.0)

0 (0.0)

1.00b

Tacrolimus

1 (2.8)

1 (5.0)

0 (0.0)

1.00b

csDMARDs combination

8 (22.2)

5 (25.0)

3 (21.4)

1.00b

Concomitant glucocorticoids, n (%)

3 (8.3)

2 (10.0)

1 (7.1)

1.00b

Concomitant NSAIDs, n (%)

5 (13.9)

4 (20.0)

1 (7.1)

0.38b

  1. Values are presented as median (interquartile range [IQR]) unless otherwise specified.
  2. aMann–Whitney U test.
  3. bFisher’s exact test.
  4. RA rheumatoid arthritis, bDMARD biological disease-modifying antirheumatic drug, anti-CCP anti-cyclic citrullinated peptide antibody, HAQ-DI Health Assessment Questionnaire-disability index, CRP C-reactive protein, ESR erythrocyte sedimentation rate, DAS28 disease activity score 28, SDAI simplified disease activity index, ACR/EULAR the American College of Rheumatology/the European League Against Rheumatism, TNF tumour necrosis factor, NSAIDs nonsteroidal anti-inflammatory drugs.