ILD related to systemic autoimmune disease

ILD_SYST_AUTO

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.

Endpoint definition

FinnGen phenotype data

321302 individuals

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Apply sex-specific rule None

321302

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Check conditions

ILD_ELSEWHERE

85

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Filter registries None

0

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Check pre-conditions, main-only, mode, ICD version None

0

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Check minimum number of events None

0

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Include endpoints

79

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ILD_SYST_AUTO

Extra metadata

First used in FinnGen datafreeze DF2

Summary Statistics

Key figures

All Female Male
Number of individuals 79 48 31
Unadjusted prevalence (%) 0.03 0.03 0.02
Mean age at first event (years) 57.36 54.52 61.76

Mortality

Follow-up Absolute risk HR [95% CI] p N
1998–2019 - - - -
15 years - - - -
5 years - - - -
1 year - - - -

Age distribution of first events

Year distribution of first events

Cumulative Incidence

Correlations

Index endpoint: ILD_SYST_AUTO – ILD related to systemic autoimmune disease
GWS hits: 1

Survival analyses between endpoints

Plot

before ILD related to systemic autoimmune disease
after ILD related to systemic autoimmune disease

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Drugs most likely to be purchased after ILD related to systemic autoimmune disease