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. 2023 Aug 2;13:12528. doi: 10.1038/s41598-023-39101-w

Table 1.

Patient background.

Characteristics Total patients
n = 33
N group
n = 11
No-N group
n = 22
p
Age (years) 75.91 ± 8.72 80.54 ± 5.76 73.59 ± 9.11 0.045
Sex 0.228
 Female/male 7/26 1/10 6/16
Smoking history 0.097
 No/yes 9/24 1/10 8/14
Baseline ILD 0.097
 No IPF/IPF 9/24 1/10 8/14
Baseline HRCT pattern
 UIP + probable 1.000
 UIP/fibrotic NSIP 30/3 10/1 20/2
Prior treatment (pirfenidone) 0.376
 No/yes 28/5 8/3 20/2
Prior treatment (prednisolone) 0.798
 No/yes 29/4 10/1 19/3
 %FVC (%)

71.15 ± 19.54

n = 24

76.02 ± 16.46

n = 10

67.68 ± 21.37

n = 14

0.313
 %DLco (%)

33.44 ± 13.58

n = 19

30.78 ± 6.97

n = 9

35.84 ± 17.64

n = 10

0.434
Serum markers at the diagnosis of AE-IPF
 P/F ratio 239.41 ± 102.75 236.26 ± 31.4710.30 240.98 ± 22.25 0.903
 WBC (/µL) 11,241.29 ± 3528.61 10,834.50 ± 4366.50 11,465.00 ± 799.59 0.642
 CRP (mg/dL) 9.32 ± 7.33 6.89 ± 6.30 10.65 ± 7.66 0.176
 D-dimer (µg/mL) 7.77 ± 11.65 5.80 ± 4.51 8.81 ± 14.06 0.517
 LDH (U/L) 360 ± 896.97 310 ± 61.56 387 ± 103.21 0.032
 KL-6 (U/L)

1339.61 ± 786.31

n = 31

1253.09 ± 240.32

n = 11

1387.20 ± 916.61

n = 20

0.657
 SP-D (mg/dL)

491.01 ± 370.36

n = 29

516.17 ± 436.08

n = 10

475.64 ± 336.75

n = 19

0.780

ILD interstitial lung disease, IPF idiopathic pulmonary fibrosis, UIP usual interstitial pneumonia, HRCT high resolution computed tomography, NSIP non-specific interstitial pneumonia, AE acute exacerbation of idiopathic pulmonary fibrosis, FVC forced vital capacity, DLco diffusing capacity for carbon monoxide, P/F ratio PaO2/FiO2 ratio, WBC white blood cell, CRP c-related peptide, LDH lactate dehydrogenase, KL-6 Krebs von den Lungen-6, SP-D surfactant protein-D.