Table 1

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

CharacteristicIPF with emphysema (n=29)IPF alone
(n=33)
P value
Age, years74±676±80.20
Male, n (%)28 (97%)20 (60%)
Body mass index21.9±3.2 (n=25)22.7±4.3 (n=29)0.40
Smoking status
 Smokers, n (%)29 (100%)14 (42%)<0.001
 Pack-years59±6812±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 functionsn=20n=17
 FVC (L)2.26±0.681.54±0.610.045
 FVC, %predicted69.4±20.356.8±22.40.002
 FEV1 (L)1.9±0.51.3±0.40.001
 FEV1/FVC (%)85.9±7.689.3±9.20.11
Thoracic CT
 CT pattern (2018 IPF guideline)
 Definite/probable/
 indeterminate/alternative
21/7/0/114/19/0/00.08
 Low-attenuation area score5.8±2.00.0±0.0< 0.001
Treatment, n (%)
 Prednisolone7 (24%)8 (24%)0.99
 Antifibrotic agents6 (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.