Table 1 Baseline characteristics of patients.

From: Association of rs3750920 polymorphism in TOLLIP with clinical characteristics of fibrosing interstitial lung diseases in Japanese

 

All patients

No

102

Age, years

73 ± 7

Sex, male, n

76 (75%)

Smoking history, yes, n

71 (70%)

Clinical diagnosis of fibrosing ILD, n

IPF

75 (74%)

NSIP

10 (10%)

CTD-ILD

6 (6%)

HP

2 (2%)

UCIP

3 (3%)

PPFE

6 (6%)

Laboratory data

LDH, IU/L

251 ± 60

SP-D, ng/dL

277 ± 227

KL-6, U/mL

1091 ± 799

Pulmonary function testing

FVC, mL

2356 ± 882

%FVC, %

77.9 ± 24.9

FEV1%, %

80.0 ± 18.1

%DLco, %

64.8 ± 22.5

  1. Data are presented as mean ± SD.
  2. ILD interstitial lung diseases, IPF idiopathic pulmonary fibrosis, NSIP non-specific interstitial pneumonia, CTD-ILD connective tissue disease–associated interstitial lung disease, HP fibrotic hypersensitivity pneumonitis, UCIP unclassifiable interstitial lung disease, PPFE pleuroparenchymal fibroelastosis, LDH lactate dehydrogenase, SP-D surfactant protein-D, KL-6 Krebs von den Lungen-6, FVC forced vital capacity, FEV forced expiratory volume in 1 s, DLco diffusing capacity for carbon monoxide.
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