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Table 1 Clinical and paraclinical data as well as therapeutic details for jDM and aDM patients

From: Differential roles of hypoxia and innate immunity in juvenile and adult dermatomyositis

Age (mean ± SD)

 

juvenile (n = 15)

adult (n = 21)

NC (n = 10)

8 +/4 years

57 +/15 years

7 +/6 years and 45 +/11 years

Gender

female

47 % (7)

67 % (14)

30 % (3)

male

53 % (8)

33 % (7)

70 % (7)

Biopsy location

M. deltoideus

 

57 % (12)

50 % (5)

M. quadriceps

87 % (13)

5 % (1)

 

unknown

13 % (2)

38 % (8)

50 % (5)

CK

normal

20 % (3)

14 % (3)

100 % (10)

>1-fold

60 % (9)

29 % (6)

 

>10-fold

13 % (2)

38 % (8)

unknown

7 % (1)

19 % (4)

Symptoms

typical skin rash

73 % (11)

52 % (11)

 

dysphagia

20 % (3)

10 % (2)

20 % (2)a

muscle weakness

73 % (11)

67 % (14)

20 % (2)a

muscle pain

60 % (9)

52 % (11)

50 % (5)a

others

27 % (4)

38 % (8)

 

unknown

13 % (2)

5 % (1)

Duration of

in months

5 +/4 (11)

3 +/3 (10)

7 +/1 (4)

symptoms

>1 years

7 % (1)

5 % (1)

20 % (2)

unknown

20 % (3)

48 % (10)

19 % (4)

Tubuloreticular formations (EM)

positive

53 % (8)

76 % (16)

n.d.

unknown

47 % (7)

24 % (5)

 

MSAs

positive

7 % (1)

19 % (4)

n.d.

negative

67 % (10)

33 % (7)

 

unknown

26 % (4)

48 % (10)

Clinical outcome

remission

53 % (8)

29 % (6)

 

improvement

20 % (3)

10 % (2)

remitting-relapsing

27 % (4)

10 % (2)

no improvement

0 % (0)

5 % (1)

 

unknown

0 % (0)

48 % (10)

100 % (10)

  1. asubjective complaints which could not be substantiated by clinical or ancillary exams, n.d. not done