TABLE 1

Baseline demographics of patients with interstitial lung disease (ILD)

CombinedANA-seropositiveANA-seronegativep-value#
Age years64.7±12.364.1±12.465.5±12.10.045
Male622 (49.2)362 (58.2)260 (41.8)0.789
BMI kg·m−229.8±6.629.6±6.730.1±6.50.251
Race/ethnicity
 Caucasian918 (72.6)515 (56.1)403 (43.9)0.004
 African American203 (16.0)147 (72.4)56 (27.6)<0.001
 Hispanic65 (5.1)50 (76.9)15 (23.1)0.002
 Asian47 (3.7)25 (53.1)22 (46.8)0.445
 Other32 (2.5)4 (12.5)28 (87.5)<0.001
Lung function
 TLC %71.3±18.669.0±17.274.8±20.0<0.001
 FVC %66.3±19.064.1±18.469.5±19.4<0.001
DLCO %51.0±21.750.0±21.852.5±21.60.065
ILD subtype
 IPF402 (31.8)212 (52.7)190 (47.3)0.003
 IPAF177 (14.0)141 (79.7)36 (20.3)<0.001
 CTD-ILD240 (19.0)177 (73.8)63 (26.3)<0.001
 HP141 (11.2)82 (58.2)59 (41.8)0.914
 Other ILD96 (7.5)29 (30.2)67 (69.8)<0.001
 Unclassifiable ILD209 (16.5)100 (47.8)109 (52.2)0.001

Data are presented as mean±sd or n (%), unless otherwise stated. Exception for participants: age n=1265, gender n=1265, antinuclear antibody (ANA) serologies n=1265, body mass index (BMI) n=1122, total lung capacity (TLC) n=989, forced vital capacity (FVC) n=1162, diffusing capacity of the lung for carbon monoxide (DLCO) n=1115, other ILD n=95. IPF: idiopathic pulmonary fibrosis; IPAF: interstitial pneumonia with autoimmune features; CTD-ILD: connective tissue disease associated ILD; HP: hypersensitivity pneumonitis. #: based on univariate analysis for categorical variables, e.g. Caucasian compared to non-Caucasian, IPF compared to non-IPF, etc; p-value based on two-tailed t-test for continuous variables, e.g. age, BMI; : include pneumoconiosis, lymphocytic interstitial pneumonia, Langerhans cell histiocytosis, cryptogenic organising pneumonia, lymphangioleiomyomatosis and other less common ILDs with small sample sizes.