Interstitial lung disease endpoints
Description
interstitial lung disease: A diverse group of lung diseases that affect the lung parenchyma. They are characterized by an initial inflammation of pulmonary alveoli that extends to the interstitium and beyond leading to diffuse pulmonary fibrosis. Interstitial lung diseases are classified by their etiology (known or unknown causes), and radiological-pathological features.
Data source
| FinnGen phenocode | ILD_ENDPOINTS |
| Include | ILD, IPF, ILD_SYST_AUTO |
| First defined in version | DF2 |
Key figures
| Sex | All | Female | Male |
| Number of individuals | 16604 | 10056 | 6548 |
| Unadjusted prevalence (%) | 9.52 | 10.14 | 8.71 |
| Mean age at first event (years) | 47.38 | 46.29 | 49.06 |
| Case fatality at 5-years (%) | 3.0 | 2.09 | 4.4 |
Longitudinal metrics
| Sex | All | Female | Male |
| Median nb. of events per indiv. | 4 | 4 | 4 |
| Recurrence at 6 months (%) | 61.77 | 61.82 | 61.68 |
Associations
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