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Table 2 Patient characteristics in 31 children with idiopathic inflammatory myositisa

From: Myositis autoantibodies in a racially diverse population of children with idiopathic inflammatory myopathies

 

White (n = 8)

Black/Hispanic (n = 23)

p-value

Age at diagnosis (years)

8.5 [3,11]

4 [3,9]

0.31

Female sex

8 (100%)

17 (73.9%)

0.30

Diagnosis

 JDM

8 (100%)

20 (87%)

0.55

 Overlap/JPM

0

3 (13%)

Disease duration (months)

48 [18,102]

27 [15,73]

0.22

Weakness

 None/mild

6 (71.4%)

14 (70%)

> 0.99

 Moderate/severe

2 (28.6%)

5 (30%)

Skin rash

 None

0

5 (25%)

0.48

 Typical

6 (85.7%)

11 (55%)

 Atypical

1 (14.3%)

4 (20%)

MSA/MAA

 Antibody negative

2 (25%)

0

0.04

 Anti-MDA5

0

8 (34.8%)

 Anti-p155/140

3 (37.5%)

4 (17.4%)

 Anti-MJ

3 (37.5%)

3 (13%)

 Anti-Mi2

0

1 (4.4%)

 Anti-synthetase (PL-12)

0

1 (4.4%)

 Anti-Ro

0

4 (17.4%)

 Anti-RNP

0

1 (4.4%)

 Anti-PM-Scl

0

1 (4.4%)

Disease features

 Ulceration

0

7 (33.3%)

0.14

 Calcinosis

2 (28.6%)

7 (33.3%)

> 0.99

 Lipodystrophy

0

3 (14.3%)

0.55

 Gastrointestinal

1 (14.3%)

8 (38.1%)

0.37

 Cardiac

0

3 (13.6%)

> 0.99

 Pulmonary

0

11 (50%)

0.03

Disease Course

 Hospitalizationsb

0

7 (38.1%)

0.08

 Death

0

1 (4%)

> 0.99

  1. Abbreviations: JDM Juvenile Dermatomyositis, JPM Juvenile Polymyositis, MSA Myositis-specific autoantibody, MAA Myositis-associated autoantibody
  2. aVariables are expressed as median (interquartile range) and frequency (percentages)
  3. bRepresents the number of patients requiring hospitalization during their disease course