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Table 1 Clinical characteristics of participants with Juvenile idiopathic arthritis (JIA) in relation to temporomandibular disorder (TMD)

From: Prevalence of temporomandibular disorder in children and adolescents with juvenile idiopathic arthritis – a Norwegian cross- sectional multicentre study

 

Total cohort

TMD

No TMD

n = 221

n = 88

n = 133

Value

Value

Value

Girls, n (%)

132 (59.7)

61 (69.3)

71 (53.4)

Age at onset, median (IQR)

6.1 (8.1, 2.3–10.4)

6.8 (8.4, 0.7–14.2)

5.2 (7.2, 0.9–14.7)

Age at visit by paediatric rheumatologists at the hospital, median (IQR)

12.7 (5.3, 9.4–14.7)

13.1 (3.3, 5.2–16.1)

11.7 (6.5, 4.8–16.5)

Disease duration, median (IQR)

4.6 (5.7, 2.6–8.3)

4.6 (6.0, 0.2–14.2)

4.6 (5.5, 0.2–14.7)

JIA categories, n (%)

 Oligoarthritis persistent

77 (34.8)

27 (30.7)

50 (37.6)

 Oligoarthritis extended

21 (9.5)

11 (12.5)

10 (7.5)

 Systemic arthritis

7 (3.2)

2 (2.3)

5 (3.8)

 RF negative polyarthritis

49 (22.2)

17 (19.3)

32 (24.1)

 RF positive polyarthritis

4 (1.8)

2 (2.3)

2 (1.5)

 Psoriatic arthritis

9 (4.1)

6 (6.8)

3 (2.3)

 Enthesitis-related arthritis

23 (10.4)

9 (10.2)

14 (10.5)

 Undifferentiated JIA

31 (14.0)

14 (15.9)

17 (12.8)

Ongoing medication, n (%)

 No DMARDs

75 (33.9)

26 (11.8)

49 (22.2)

 sDMARDs*

 60 (27.1) 

23 (10.4)

37 (16.7)

 bDMARDs**

 86 (38.9)

39 (17.6)

47 (21.3)

  1. JIA Juvenile idiopathic arthritis, TMD Temporomandibular disorder
  2. *sDMARDs = Synthetic disease-modifying antirheumatic- drugs; methotrexate, mykofenolatmofetil, **bDMARDs = Biologic disease-modifying antirheumatic-drugs; etanercept, infliximab, adalimumab, tocilizumab, abatacept, certolizumab, golimumab