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Table 1 Baseline characteristics of the study sample

From: Induction of sustained remission in early inflammatory arthritis with the combination of infliximab plus methotrexate: the DINORA trial

 

IFX + MTX

MTX

PL

P value

Number of patients (n)

38

36

16

0.4440

Female

26 (68.4%)

28 (77.8%)

9 (56.3%)

0.2833

Age (years), mean ± SD

52.1 ± 14.1

52.9 ± 14.0

54.4 ± 11.2

0.9170

Symptom duration (weeks)a, mean ± SD

10.3 ± 2.3

9.4 ± 2.3

9.8 ± 1.8

0.0722

Rheumatoid factor positive

13 (34.2%)

13 (36.1%)

7 (43.8%)

0.7988

Patients who used steroids prior to the study

24 (63.2%)

22 (61.1%)

9 (56.3%)

0.8931

Anti-citrullinated protein antibody positive

18 (47.4%)

16 (44.4%)

7 (43.8%)

0.9563

Patients who meet the ACR/EULAR 2010 classification criteria for RA, 2010 [25]

26 (68%)

19 (53%)

12 (75%)

0.2135

Patients who meet the 1987 ARA classification criteria for RA [35]

22 (58%)

19 (53%)

9 (56%)

0.9049

Health Assessment Questionnaire (0–3)

0.9 ± 0.7

0.9 ± 0.6

0.7 ± 0.7

0.2903

Disease Activity Score 28 (DAS28; based on ESR)

5.0 ± 1.4

4.8 ± 1.3

4.7 ± 1.1

0.8464

Simplified Disease Activity Index (SDAI)

34.3 ± 23.8

31.1 ± 14.4

27.5 ± 20.0

0.4771

Clinical Disease Activity Index (CDAI)

25.1 ± 14.7

26.2 ± 13.9

23.5 ± 11.9

0.8951

Swollen joint count (0–28)

7.2 ± 5.7

6.50 ± 5.1

7.4 ± 4.6

0.7048

Tender joint count (0–28)

9.2 ± 7.3

10.3 ± 7.2

7.8 ± 5.6

0.5263

Visual analogue scale pain (mm)

44.0 ± 29.3

44.2 ± 24.3

44.6 ± 22.7

0.9595

Patient global assessment (mm)

48.6 ± 29.0

47.8 ± 24.7

39.6 ± 21.0

0.5274

Evaluator/physician global assessment (mm)

38.6 ± 18.3

46.3 ± 22.3

44.6 ± 20.7

0.3627

C-reactive protein (mg/dl)

1.71 ± 2.40

1.18 ± 1.88

0.98 ± 1.28

0.5567

Erythrocyte sedimentation rate (ESR; mm/h)

23.2 ± 20.3

20.3 ± 21.2

20.4 ± 12.6

0.8129

Total Sharp-van-der-Heide score

2.8 ± 5.4

3 ± 3.8

4.6 ± 8.6

0.4816

Erosion score

1.2 ± 1.8

1.6 ± 2.2

2.2 ± 4.2

0.6019

Joint space narrowing score

1.6 ± 3.8

1.4 ± 2.2

2.4 ± 4.4

0.5658

  1. Data are shown as mean ± standard deviation or n (%) as appropriate
  2. The parameters showed no significant differences between the three groups at baseline
  3. Tables with additional data on baseline characteristics as well as 1-year data for the patients who were in remission at 1 year are provided in Additional file 2 (Tables SC and SD)
  4. ACR American College of Rheumatology, ARA American Rheumatism Association, EULAR European League Against Rheumatism, IFX infliximab, MTX methotrexate, PL placebo, RA rheumatoid arthritis
  5. aSymptom duration refers to the first visit when the patients presented themselves at the centres. At the baseline visit, symptom duration of all patients was 12 weeks because baseline visits were scheduled at this time to ensure persistent arthritis for 12 weeks. Patients who had no residual arthritis at the baseline visit were excluded