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Table 1 Characteristics of the examined number of patients in disease-stratified groups.

From: Angiogenic activity of sera from interstitial lung disease patients in relation to pulmonary function

 

No. of subjects

Age (yr)

Female/Male

Smokers/non-smokers

Sarcoidosis

83

40 ± 12

35/48

20/63

IPF

31

61 ± 12

14/17

9/22

EAA

29

47 ± 16

13/16

8/21

CVD

16

55 ± 11

7/9

4/12

SCL

13

51 ± 12

11/2

1/12

WG

14

49 ± 18

12/2

3/11

PLH

12

37 ± 13

4/8

12/0

Silicosis

12

43 ± 9

1/11

8/4

DIPF

10

63 ± 11

3/7

1/9

COP

5

58 ± 8

3/2

1/4

Healthy volunteers

36

39 ± 11

22/14

4/32

  1. IPF - idiopathic pulmonary fibrosis, EAA - extrinsic allergic alveolitis, CVD - collagen vascular diseases, SCL - scleroderma, WG - Wegener's granulomatosis, PLH - pulmonary Langerhans cells histiocytosis, DIPF - drug-induced pulmonary fibrosis, COP - cryptogenic organizing pneumonia.