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Table 2 Baseline characteristics of patients in 2 mg and 4 mg groups before and after propensity score matching

From: Efficacy and safety of baricitinib in rheumatoid arthritis patients with moderate renal impairment: a multicenter propensity score matching study

 

Before matching

After matching

2 mg

4 mg

P value

2 mg

4 mg

P value

Number of cases

53

86

 

33

33

 

Age (y)

61.3 ± 12.1

57.4 ± 15.5

0.106

59.2 ± 11.8

59.5 ± 14.6

0.934

Sex

46 women; 7 men

69 women; 17 men

0.306

26 women; 7 men

25 women; 8 men

0.769

Height (cm)

154.2 ± 9.8

153.4 ± 7.8

0.425

153.2 ± 6.7

155.2 ± 4.8

0.798

Weight (kg)

55.7 ± 9.8

56.8 ± 10.2

0.582

55.7 ± 9.4

56.2 ± 9.2

0.824

BMI (kg/m2)

22.9 ± 3.29

23.0 ± 3.40

0.84

23.2 ± 3.19

22.9 ± 2.80

0.756

Disease duration (years) (± SD)

15.4 ± 12.0

9.9 ± 8.5

0.004*

11.6 ± 8.4

11.3 ± 8.2

0.868

Tender joint count (out of 28 joints)

4.2 ± 3.5

5.0 ± 5.5

0.28

3.7 ± 2.9

3.0 ± 3.3

0.365

Swollen joint count (out of 28 joints)

2.8 ± 3.1

2.6 ± 2.4

0.77

2.3 ± 2.7

2.3 ± 2.0

0.958

CRP (mg/dl)

1.8 ± 2.2

1.4 ± 2.5

0.405

1.5 ± 1.6

1.4 ± 2.9

0.938

Physician VAS (± SD)

42.8 ± 21.7

38.5 ± 23.0

0.289

38.1 ± 20.0

32.5 ± 22.6

0.289

Patient VAS (± SD)

46.3 ± 25.7

44.3 ± 26.8

0.669

43.7 ± 26.8

36.9 ± 27.5

0.316

CDAI

15.8 ± 8.0

15.8 ± 9.6

0.98

14.2 ± 7.8

12.3 ± 7.6

0.311

SDAI

17.6 ± 9.3

17.3 ± 10.1

0.853

15.6 ± 8.3

13.7 ± 8.5

0.349

MTX Dosage (mg/week)

3.9 ± 4.0

5.8 ± 5.0

0.017*

4.4 ± 4.3

5.9 ± 4.6

0.163

PSL dosage (mg/day)

2.9 ± 2.8

2.5 ± 3.4

0.44

3.0 ± 2.8

2.4 ± 3.5

0.395

Rheumatoid factor positive rate

74.8

71.9

0.66

73.8

72.2

0.662

Anti-CCP antibody positive rate (%)

50.4

75.6

0.0453*

72.7

78.8

0.566

BIO use history: 1 drug

11

23

 

6

12

 

BIO use history: 2 drugs

10

20

 

6

9

 

BIO use history: 3 or more drugs

17

30

 

11

5

 

eGFR

46.3 ± 12.9

79.1 ± 17.2

 

43.6 ± 14.2

82.1 ± 20.4

 
  1. * P < 0.05