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Table 1 General characteristics of 91 adult patients with defined dermatomyositis

From: Clinical manifestations, outcomes, and antibody profile of Brazilian adult patients with dermatomyositis: a single-center longitudinal study

Characteristics

N = 91

Age at disease diagnosis (years)

47.3 ± 15.4

Female gender

61 (67.0)

White ethnicity

74 (81.3)

Constitutional symptoms at baseline

81 (89.0)

Gottron’s sign/papules

87 (96.7)

Heliotrope rash

79 (86.8)

“V”-neck sign

71 (78.0)

“Shawl” sign

56 (61.5)

Raynaud’s phenomenon

55 (60.4)

Vasculitis

26 (28.6)

“Mechanics’ hands”

20 (21.0)

Skin ulcers

15 (16.5)

Calcinosis

4 (4.4)

Muscle strength (MRC)

 

 Upper limbs

 

  V degree

1 (1.1)

  IV degree

61 (67.0)

  III degree

23 (25.3)

  II degree

6 (6.6)

 Lower limbs

 

  V degree

5 (5.5)

  IV degree

56 (61.6)

  III degree

24 (26.4)

  II degree

6 (6.6)

Dysphagia

67 (73.6)

Arthritis

30 (33.0)

Lung involvement

34 (37.4)

 Interstitial pneumopathy

32 (35.2)

 Ground glass opacities

12 (13.2)

 Pneumomediastinum

1 (1.1)

Maximum levels of muscle enzymes

 

 Creatine phosphokinase (U/L)

812 (177–3121)

 Aspartate aminotransferase (U/L)

62 (26–32)

 Alanine aminotransferase (U/L)

43 (21–98)

 Lactic dehydrogenase (U/L)

531 (248–904)

Antinuclear antibodies

62 (68.2)

 Myositis-specific autoantibodies (N = 74)

 

  Anti-Mi-2

10 (11.0)

  Anti-Jo-1

10 (11.0)

  Anti-MDA-5

10 (11.0)

  Anti-TIF-1γ

7 (7.7)

  Anti-SAE

6 (6.6)

  Anti-NXP-2

5 (5.5)

 Myositis-associated autoantibodies (N = 74)

 

  Anti-Ro-52

26 (28.6)

  Anti-PM/Scl 75

3 (3.3)

  Anti-SRP

1 (1.1)

  Anti-OJ, -EJ, PL-7, PL-12, -Ku

3 (3.3)

  1. Data are expressed as mean ± standard deviation, median (IQR 25th–75th), or percentage (%)