Skip to main content

Table 1 Patient group data summary and total Wnt7B area reactivity

From: WNT7B in fibroblastic foci of idiopathic pulmonary fibrosis

Patient ID

Area Total μm2/mm2

Path Diagnosis FVC > 80%

Patient ID

Area Total μm2/mm2

Path Diagnosis FVC > 50% < 80%

Patient ID

Area Total μm2/mm2

Path Diagnosis FVC < 50%

34/1

0

Normal

22/29

0.22660864

Mild IF

53/13

0.308239253

Mild IF

50/8

0

Normal

52/59

0.46500093

Mild IF

40/11

0.318122907

Mild IF

60/9

0

Normal

9/55

0.702668072

IPF

51/7

0.421600843

IPF/UIP

29/25

0

Normal

46/51

0.792223807

IPF

32/28

0.543860737

IPF/UIP

27/26

0

Normal

3/50

0.853712645

Severe IF

11/12

0.609837285

IPF/UIP

43/16

0

Normal

39/43

0.898132637

IPF/UIP

2/38

0.689568308

IPF/UIP

33/23

0

Normal

30/17

0.984128952

IPF/UIP

38/35

0.870788258

IPF/UIP

13/39

0

Mild emphysema

58/15

1.02457832

Mild IF

19/47

1.07500215

Mild IF

47/44

0

Normal

54/34

1.124896765

IPF/UIP

23/31

1.246080924

Inf/Honeycombing

31/45

0

Normal

12/19

1.127274982

Severe IF

48/53

1.332033914

Mild IF

20/46

0

Normal

55/5

1.135880134

Mild IF

35/10

1.451763467

IPF/UIP

28/49

0

Mild emphysema

15/4

1.19162088

Mild IF

16/21

1.506947458

IPF/UIP

5/52

0

Septal thickening

42/32

1.257089128

IPF/UIP

49/20

1.597695503

Mild IF

1/57

0

Normal

45/18

1.470515762

IPF/UIP

4/41

1.698264266

IPF/UIP

7/60

0

Normal

36/33

1.5500031

IPF/UIP

10/22

2.0666708

Mild IF

57/36

0

Mild emphysema

24/42

1.667114445

IPF/UIP

25/40

2.214.290

IPF/UIP

14/3

0.077500155

A telectasis/thickening

37/30

2.258029207

IPF/UIP

21/37

2.188697845

Mild IF

8/27

0.116043013

Normal

18/2

2.294004588

DIFFUSEIF

56/24

2.279055942

IPF/UIP

41/14

0.41333416

Normal

44/56

2.679444431

IPF/UIP

17/48

2.605680887

IPF/UIP

   

59/58

3.620364384

IPF/UIP

   

avg

0.031940912

 

avg

1.366149591

 

avg

1.267217264

 

stdev

0.097448895

 

stdev

0.808903868

 

stdev

0.71592836

 
  1. Legend: IF – interstitial fibrosis; IPF – idiopathic pulmonary fibrosis; UIP – usual interstitial pneumonia.