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Table 3 Characteristics of nr-axSpA patients at initiation of first TNFi treatment with available follow-up visit at 1 year (patients with co-morbid fibromyalgia excluded)

From: Differences between men and women with nonradiographic axial spondyloarthritis: clinical characteristics and treatment effectiveness in a real-life prospective cohort

Parameter

A. Nr-axSpA patients with available follow-up visit at 1 year

B. Nr-axSpA patients still on TNFi treatment at 1 year

N, 120

Men, N = 58

Women, N = 62

p

N, 83

Men, N = 45

Women, N = 38

p

Age, years

120

36.0 (10.8)

38.6 (11.4)

0.25

83

34.6 (10.3)

39.2 (13.4)

0.16

Age at onset, years

120

27.7 (8.4)

27.9 (8.2)

0.78

83

27.4 (8.0)

27.4 (7.5)

0.89

Symptom duration, years

120

8.3 (9.5)

10.7 (11.3)

0.27

83

7.2 (7.8)

11.7 (12.2)

0.12

Diagnostic delay, years

120

4.7 (8.6)

7.3 (10.1)

0.03

83

3.0 (5.3)

7.4 (10.3)

0.02

HLA-B27 positive, %

110

79.6

73.2

0.50

78

83.3

77.8

0.58

Prior sacroiliitis on MRI, %

112

67.9

67.8

1.00

77

66.7

65.7

1.00

BASDAI

108

5.4 (2.0)

6.1 (1.6)

0.05

74

5.2 (2.0)

5.9 (1.6)

0.09

Physician Global Assessment

115

5.1 (1.9)

4.8 (1.7)

0.54

81

5.3 (2.0)

4.7 (1.8)

0.28

Patient Global Assessment

109

6.6 (2.2)

6.7 (1.9)

1.00

75

6.5 (2.2)

6.4 (2.0)

0.89

ASDAS

100

3.4 (0.9)

3.4 (0.7)

0.63

69

3.4 (0.9)

3.4 (0.6)

0.90

ASDAS > 2.1, %

100

88.9

94.5

0.46

69

91.7

97.0

0.62

CRP (mg/l), median (IQR)

111

7.0 (2.0; 15.0)

7.0 (3.0; 10.0)

0.63

77

7.3 (3.0; 19.5)

7.0 (3.5; 10.5)

0.37

Elevated CRP, %

111

47.2

43.1

0.71

77

54.8

42.9

0.36

BASFI

109

3.7 (2.4)

3.5 (2.4)

0.61

75

3.5 (2.4)

3.2 (2.3)

0.53

BASMI

102

1.2 (1.1)

1.4 (1.2)

0.37

70

1.1 (1.1)

1.2 (1.3)

0.88

EQ-5D

103

53.7 (22.8)

57.6 (17.8)

0.52

70

55.6 (21.7)

59.2 (15.7)

0.65

Current periph. arthritis,%

116

47.4

47,5

1.00

82

46.7

54.0

0.66

Number of swollen joints

113

0.7 (1.2)

1.2 (2.6)

0.83

80

0.8 (1.3)

1.5 (2.9)

0.52

Current enthesitis, %

115

80.7

86.2

0.46

82

80.0

86.5

0.56

Modified MASES

114

2.4 (2.6)

3.7 (3.2)

0.02

81

2.1 (2.2)

3.4 (2.7)

0.03

Dactylitis ever, %

118

16.1

19.4

0.81

82

11.4

21.1

0.36

csDMARDs ever, %

120

31.0

40.3

0.34

83

26.7

36.8

0.35

Taking NSAIDs, %

109

94.1

86.2

0.21

76

100.0

85.7

0.02

Current smoking, %

102

28.9

15.8

0.15

68

26.5

8.8

0.11

Body mass index

120

25.9 (4.2)

24.0 (4.4)

0.002

83

25.6 (4.2)

23.6 (4.7)

0.004

Type of TNFi, %

120

  

0.69

83

  

0.38

• Adalimumab

 

34.5

43.5

  

35.6

50.0

 

• Certolizumab

 

1.7

0.0

  

2.2

0.0

 

• Etanercept

 

19.0

16.1

  

20.0

10.5

 

• Golimumab

 

22.4

24.2

  

20.0

26.3

 

• Infliximab

 

22.4

16.1

  

22.2

13.2

 
  1. A is the characteristics of patients starting TNFi included in the response/tolerance analyses: response in patients with available outcome at 1 year, patients having discontinued the first TNFi in the meantime being considered non-responders. B is the characteristics of patients starting TNFi included in the completer analyses at 1 year. Except where indicated otherwise, values are the mean (SD). Data in bold are statistically significant. Patients with co-morbid fibromyalgia were excluded from these analyses. ASDAS Ankylosing Spondylitis Disease Activity Score, BASDAI Bath Ankylosing Spondylitis Disease Activity Index, BASFI Bath Ankylosing Spondylitis Functional Index, BASMI Bath Ankylosing Spondylitis Metrology Index, CRP C-reactive protein levels, csDMARDs conventional synthetic disease-modifying anti-rheumatic drugs, EQ-5D EuroQol 5-domains, HLA-B27 human leucocyte antigen B27, MASES Maastricht Ankylosing Spondylitis Enthesitis Score, modification refers to the inclusion of the plantar fascia in the count, nr-axSpA nonradiographic axial spondyloarthritis, NSAIDs nonsteroidal anti-inflammatory drugs, TNFi tumor necrosis factor inhibitor