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. Author manuscript; available in PMC: 2022 Jan 16.
Published in final edited form as: Eur Respir J. 2020 Dec 3;56(6):2001205. doi: 10.1183/13993003.01205-2020

Table 4.

Outcome risk for ILD subgroups

ILD Subtype Unadjusted Adjusted
HR 95% CI p-value HR 95% CI p-value
Model 1 *
IPAF without MSA/MAA Ref Ref Ref Ref Ref Ref
IPAF-MSA 0.13 0.03–0.55 0.005 0.20 0.05–0.84 0.03
IPAF-MAA 0.65 0.37–1.12 0.12 0.68 0.38–1.21 0.19
IIM-ILD 0.09 0.03–0.30 <0.001 0.17 0.05–0.54 0.003
non-IIM CTD-ILD 0.37 0.25–0.55 <0.001 0.52 0.34–0.80 0.003
IPF 1.11 0.84–1.46 0.47 0.70 0.51–0.97 0.03
Model 2
IPAF-UIP Ref Ref Ref Ref Ref Ref
IPAF w/o UIP 0.37 0.23–0.61 <0.001 0.46 0.28–0.78 0.004
IPAF-MSA 0.10 0.02–0.41 0.001 0.14 0.03–0.58 0.007
IIM-ILD 0.07 0.02–0.23 <0.001 0.13 0.04–0.42 0.001
non-IIM CTD-ILD 0.28 0.19–0.42 <0.001 0.43 0.27–0.66 <0.001
IPF 0.83 0.62–1.11 0.22 0.63 0.46–0.86 0.003
*

Model 1 adjusted for center, race/ethnicity, presence of UIP, immunosuppressant exposure and GAP stage

Model 2 adjusted for center, race/ethnicity, immunosuppressant exposure and GAP stage

Abbreviations: ILD = interstitial lung disease; IPAF = interstitial pneumonia with autoimmune features; MSA = myositis specific antibody; IIM-ILD = idiopathic inflammatory myopathy-associated ILD; IPF = idiopathic pulmonary fibrosis