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Table 1 Patient demographics and clinical data. We analysed the demographic and clinical data of 22 patients with a histologically confirmed IPF diagnosis. 11 of the patients underwent VATS and had mild-to-moderate fibrotic changes in the lung. Another 11 IPF patients underwent lung transplantation because of severe or end-stage fibrosis. There was no significant difference between the patient groups’ age, smoking status and body mass index (BMI). The lung function parameters Forced Expiratory Volume in 1 s (FEV1), Forced Vital Capacity (FVC), Total Lung Capacity (TLC) and Transfer factor for carbon monoxide in the lung (TLCO) were significantly higher in the patient group with mild-to-moderate fibrotic changes compared to those with severe or end-stage fibrosis (p < 0.01 using Students unequal variance t-test)

From: Role of CD248 as a potential severity marker in idiopathic pulmonary fibrosis

 

Patients with mild-to-moderate fibrosis (VATS biopsy patients)

Patients with severe or end-stage fibrosis (Lung transplant patients)

p-value (Students t-test)

Demographic and clinical data

N

11

11

-

Sex

4 males, 7 females

9 males, 2 females

-

Median age (range)

66 (39–76)

58 (44–61)

0.126

Smoking in history (percent)

7 (63 %)

7 (63 %)

0.482

Pack years (mean ± SEM)

28.37 ± 11.97

21.93 ± 6.61

0.784

BMI (mean ± SEM)

28.87 ± 1.37

27.67 ± 1.87

0.636

Lung function

FEV1 (mean ± SEM)

2.51 ± 0.19

1.59 ± 0.20

0.0009

FVC (mean ± SEM)

3.21 ± 0.32

1.92 ± 0.23

0.0006

TLC (mean ± SEM)

4.77 ± 0.54

3.04 ± 0.34

0.0014

TLCO (mean ± SEM)

3.69 ± 0.36

2.09 ± 0.30

0.0099

Medication (given only after biopsy)

Prednisolone

6 (54.5 %)

8 (72.7 %)

-

Azathioprine

3 (27.2 %)

4 (36.3 %)

-

N-acetylcysteine

4 (36.3 %)

2 (18.1 %)

-