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Table 1 Demographic, clinical, and serological characteristics of the study population

From: Subclinical systolic and diastolic myocardial dysfunction in polyphasic polymyositis/dermatomyositis: a 2-year longitudinal study

 

IIM baseline; n=28

IIM 2 years; n=28

Control; n=26

Demography, organ involvements

 Mean age at onset, years, Mean ± SEM

41.9 ± 1.6

NA

43.7 ± 0.7

 Sex (female/male) n

25/3 (89/11%)

25/3 (89/11%)

23/3 (88/12%)

 Diagnosis (PM/DM)

21/7 (77%/23%)

21/7 (77%/23%)

NA

 Interstitial lung disease

35.7%

35.7%

NA

 Raynaud sign

32.1%

32.1%

NA

 Dysphagia

14.2%

14.2%

NA

 Arthritis

71.4%

71.4%

NA

 SBP, mmHg

120 ± 2

130 ±1

122 ±2

 DBP, mmHg

76 ± 1

78±1

73±1

 HR, beat/min

85 ± 1

79±2

76±3

Antibodies

Myositis profile 3 Blot Strip

Euroline Myositis Antigen Profile4

NA

 Anti-Jo1

6

6

NA

 Anti-PL7

0

0

NA

 Anti-PL12

0

0

NA

 Anti-EJ

0

0

NA

 Anti-OJ

0

0

NA

 Anti-SRP

0

0

NA

 Anti-Mi2

0

1

NA

 Anti-NXP2

0

2

NA

 Anti-MDA5

0

0

NA

 Anti-TIF1gamma

0

1

NA

 Anti-Pm/scl-100

1

1

NA

 Anti-Pm/scl-75

3

3

NA

 Anti-Ku

0

0

NA

 Anti-Ro52

6

6

NA

 Anti-DNS

0

0

NA

Immunsupressive therapy

 Corticosteroid

28

28

0

 Cyclosporin-A

4

4

0

 Methotrexate

0

5

0

 Cyclophosphamid

0

2

0

 Rituximab

0

2

0

Disease course

 Monophasic (without relapse) n

NA

16

NA

 Polyphasic (with relapse) n

NA

12

NA

  1. PM polymyositis (including necrotizing myopathy), DM dermatomyositis, SBP systolic blood pressure, DBP diastolic blood pressure, HR heart rate, NA not applicable