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. 2022 Sep 19;12(9):e062236. doi: 10.1136/bmjopen-2022-062236

Table 1.

Baseline characteristics in patients with idiopathic pulmonary fibrosis with or without concomitant pulmonary emphysema

Characteristic IPF with emphysema (n=29) IPF alone
(n=33)
P value
Age, years 74±6 76±8 0.20
Male, n (%) 28 (97%) 20 (60%)
Body mass index 21.9±3.2 (n=25) 22.7±4.3 (n=29) 0.40
Smoking status
 Smokers, n (%) 29 (100%) 14 (42%) <0.001
 Pack-years 59±68 12±20 <0.001
Comorbidity
 Lung cancer, n (%) 2 (7%) 1 (3%) 0.59
 Any cancer, n (%) 5 (17%) 3 (9%) 0.33
 Diabetes mellitus, n (%) 6 (21%) 10 (30%) 0.38
 Chronic heart failure, n (%) 6 (21%) 13 (39%) 0.11
 Chronic renal failure, n (%) 0 (0%) 2 (6%) 0.59
 Chronic respiratory infection, n (%) 1 (3%) 1 (3%) 0.93
Laboratory data
 KL-6 in serum (U/mL) 1266±697 (n=24) 1255±817 (n=26) 0.74
 Albumin in serum (g/mL) 3.7±0.5 (n=20) 3.7±0.3 (n=23) 0.64
Pulmonary functions n=20 n=17
 FVC (L) 2.26±0.68 1.54±0.61 0.045
 FVC, %predicted 69.4±20.3 56.8±22.4 0.002
 FEV1 (L) 1.9±0.5 1.3±0.4 0.001
 FEV1/FVC (%) 85.9±7.6 89.3±9.2 0.11
Thoracic CT
 CT pattern (2018 IPF guideline)
 Definite/probable/
 indeterminate/alternative
21/7/0/1 14/19/0/0 0.08
 Low-attenuation area score 5.8±2.0 0.0±0.0 < 0.001
Treatment, n (%)
 Prednisolone 7 (24%) 8 (24%) 0.99
 Antifibrotic agents 6 (20%) 3 (9%) 0.13

FEV1, forced expiratory volume in 1 s; FVC, forced vital capacity; IPF, interstitial pulmonary fibrosis; KL-6, Krebs von Lungen-6.