Table 7.
Odds Ratio for IPF versus Alternative Diagnoses Shown in Columns for Each Unit Increase in Index Score (Derivation and Validation IPF Cohorts)
| Adjusted* |
Unadjusted |
||||||
|---|---|---|---|---|---|---|---|
| Healthy Control Subjects | a-ILD | RA-ILD | Healthy Control Subjects | a-ILD | RA-ILD | ||
| Derivation IPF | |||||||
| OR | 1.9 | 1.9 | 1.0 | 2.7 | 2.1 | 1.1 | |
| 95% CI | 1.1–3.3 | 1.2–2.8 | 0.6–1.5 | 2.0–3.6 | 1.4–3.0 | 0.7–1.6 | |
| P value | 0.015 | 0.005 | 0.82 | <0.0001 | 0.0001 | 0.65 | |
| Validation IPF |
|||||||
| OR | 2.7 | 2.3 | 0.8 | 3.2 | 2.5 | 1.0 | |
| 95% CI | 1.5–4.7 | 1.3–3.9 | 0.5–1.5 | 2.2–4.6 | 1.6–4.0 | 0.6–1.8 | |
| P value | 0.0009 | 0.004 | 0.56 | <0.0001 | 0.0001 | 0.89 | |
Definition of abbreviations: a-ILD = alternative interstitial lung disease; CI = confidence interval; IPF = idiopathic pulmonary fibrosis; OR = odds ratio comparing 0 to 3 point index score delineations in each row; RA-ILD = rheumatoid arthritis–associated interstitial lung disease.
Adjustment variables include sex, age, smoking status, and FVC (% predicted).