Skip to main content

Table 1 Demographic, clinical, radiological, and laboratory characteristics of the study population and comparison of the survived and dead patients

From: Elevations in NLR at the first year of pirfenidone treatment may be associated with worse prognosis in patients with idiopathic pulmonary fibrosis

Characteristics

Total study population (n =  125)

Survived(n =  53)

Non-survived(n =  72)

p

Age, mean ± SD

67.9 ± 7.27

67.5 ± 7.27

68.2 ± 7.31

0.55

Sex, male, n (%)

100 (80)

42 (79.2)

58 (80.6)

1.00

Smoking, n (%)

84 (67.2)

32 (61.5)

52 (72.2)

0.25

Smoking packet-years, mean ± SD

39.8 ± 35.0

34.6 ± 21.7

42.9 ± 40.8

0.32

Family history of IPF, n(%)

8 (6.4)

2 (3.8)

6 (8.3)

0.47

Comorbidities, n(%)

70 (56)

26 (49.1)

44 (61.1)

0.21

Diabetes mellitus, n(%)

27 (21.6)

8 (15.1)

19 (26.4)

0.19

Hypertension, n(%)

28 (22.4)

12 (22.2)

16 (22.6)

1.00

Cardiovascular disease, n(%)

39 (31.2)

14 (26.4)

25 (34.7)

0.34

COPD, n(%)

15 (12)

4 (7.5)

11 (15.3)

0.27

Lung cancer, n(%)

6 (4.8)

0

6 (8.3)

0.04

Clubbing, n (%)

26 (20.8)

8 (15.4)

18 (25)

0.26

IPF exacerbation history

8 (6.4)

0

8 (11.1)

0.02

Body mass index, kg/m2, mean ± SD

27.9 ± 3.98

28.3 (3.32)

27.6 (4.40)

0.33

FVC, lt, mean ± SD

2.35 ± 0.69

2.51 ± 0.75

2.23 ± 0.61

0.02

DLCO, mmol/kPa/min, mean ± SD

3.96 ± 1.60

4.43 (2.67)

3.11 (1.49)

 < 0.001

Laboratory

 Hemoglobin, g/dl, mean ± SD

13.94 ± 1.43

13.8 ± 1.17

14.02 ± 1.6

0.48

 Leucocytes, /mm3, median (IQR)

8300 (2600)

7950 (2975)

8700 (2450)

0.20

 Neutrophils, /mm3, median (IQR)

5250 (2050)

4900 (1950)

5550 (1950)

0.21

 Lymphocytes, /mm3, median (IQR)

2100 (1000)

2100 (775)

2150 (1200)

0.54

 Platelets, /mm3, median (IQR)

257,000 (92,500)

237,000 (95,250)

260,000 (95,500)

0.17

 CRP, mg/dl, median (IQR)

0.47 (0.62)

0.31 (0.70)

0.58 (0.53)

0.004

 NLR, median (IQR)

2.3 (1.7)

2.32 (1.30)

2.43 (1.89)

0.70

 PLR, median (IQR)

119.4 (64.3)

121.1 (58.2)

118.2 (75.5)

0.87

 NLR, 1st year, median (IQR)

2.5 (1.8)

2.39 (1.4)

2.75 (1.88)

0.13

 PLR, 1st year, median (IQR)

130 (70.5)

113.3 (54.0)

136.7 (82.1)

0.16

 Biopsy proven disease, n(%)

30 (24)

18 (34)

12 (16.7)

0.03

 HRCT, definite UIP pattern, n(%)

92 (73.6)

33 (62.3)

59 (81.9)

0.02

 Honeycombing, n(%)

93(74.4)

34 (64.2)

59 (81.9)

0.04

 Traction bronchiectasis, n(%)

71 (56.8)

22 (41.5)

49 (68.1)

0.004

 Emphysema, n(%)

19 (15.2)

9 (17)

10 (13.9)

0.80

 Home oxygen treatment, n(%)

23 (18.4)

1 (1.9)

22(30.6)

 < 0.001

Antifibrotic treatment

 Pirfenidon, n(%)

68 (54.4)

26 (49.1)

42 (58.3)

0.37

 Nintedanib, n(%)

57 (45.6)

27 (50.9)

30 (41.7)

0.37

 Clinical progression, n(%)

10 (8)

3 (6.3)

7 (10.1)

0.52

 Treatment cessation, n(%)

24 (19.2)

7 (14.6)

18 (26.1)

0.17

 GAP stages II or III, n(%)

75 (60)

23 (43.4)

52 (72.2)

0.002

  1. SD standard deviation, IPF idiopathic pulmonary fibrosis, COPD chronic obstructive pulmonary disease, FVC forced vital capacity, DLCO diffusion capacity of lungs, IQR interquartile range, CRP C-reactive protein, NLR neutrophil-to-lymphocyte ratio, PLR platelet-to-lymphocyte ratio, HRCT high-resolution computed tomography, UIP usual interstitial pneumonia, GAP gender-age-physiology