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. Author manuscript; available in PMC: 2023 Jun 1.
Published in final edited form as: Lancet Respir Med. 2022 Jan 18;10(6):593–602. doi: 10.1016/S2213-2600(21)00503-8

Table 1:

Baseline characteristics and outcomes for the discovery and validation cohorts

Discovery cohort (n=385) Validation cohort (n=204) p value
Age, years 63·6 (12·7) 60·7 (11·6) 0·0085
Sex
 Female 228 (59%) 124 (61%) ..
 Male 157 (41%) 80 (39%) 0·71
Race or ethnicity
 White 273 (71%) 151 (74%) 0·42
 Black 15 (4%) 26 (13%) <0·0001
 Hispanic 55 (14%) 21 (10%) 0·17
 Asian 32 (8%) 6 (3%) 0·012
 Mixed or other 10 (3%) 0 0·02
Years from diagnosis to blood draw <0·001
 <1 292 (76%) 44 (22%) ..
 1 33 (9%) 56 (27%) ..
 2 19 (5%) 42 (21%) ..
 3 8 (2%) 27 (13%) ..
 >3 33 (9%) 35 (17%) ..
Ever smoker 259 (67%) 114 (56%) 0·0063
ILD classification
 CTD-ILD 148 (38%) 97 (48%) 0·033
  Systemic sclerosis ILD 42 (11%) 30 (15%) 0·67
  Rheumatoid arthritis ILD 38 (10%) 21 (10%) 0·47
  Idiopathic inflammatory myopathy ILD 42 (11%) 26 (13%) 0·79
  Other CTD-ILD 26 (9%) 20 (10%) 0·55
 Chronic hypersensitivity pneumonitis 185 (48%) 57 (28%) <0·0001
 Unclassifiable ILD 52 (14%) 50 (25%) 0·0008
Pulmonary function
 FVC, % predicted 64·4 (18·4) 62·5 (19·2) 0·23
 DLCO, % predicted 46·7 (17·3) 40·7 (17·7) 0·0002
High-resolution CT pattern
 Definite or probable UIP 75 (19%) 60 (29%) 0·0063
 Non-specific interstitial pneumonia 111 (29%) 101 (50%) <0·0001
 Other pattern 199 (52%) 43 (21%) <0·0001
Outcomes
 ILD progression 164 (43%) 92 (45%) 0·56
  Death 59 (15%) 32 (16%) 0·91
  Lung transplant 6 (2%) 12 (6%) 0·0037
  ≥10% FVC decline 99 (26%) 48 (24%) 0·56
 Months to progression 6·7 (3·5–9·5) 7·0 (4·0–9·3) 0·69

Data are mean (SD), n (%), or median (IQR). ILD=interstitial lung disease. CTD-ILD=connective tissue disease-associated ILD. FVC=forced vital capacity. DLCO=diffusion capacity of the lung for carbon monoxide. UIP=usual interstitial pneumonia.