Incident patients with idiopathic pulmonary fibrosis (IPF) in Denmark will be offered inclusion and followed up for up to 5 years with measurements of blood biomarkers and measurements of disease progression.
IPF pathogenesis is complex, including epithelial injury, resident fibroblast-myofibroblast transformation, recruitment of fibrocytes, macrophage activation, and release of numerous cytokines and chemokines. Several of these processes release potential biomarker proteins into the blood stream or onto the epithelial surface where they can be measured. Biomarkers have mainly two potential roles in IPF. Firstly, a diagnostic biomarker would distinguish IPF from other diseases with similar symptoms, facilitating diagnosis and possibly decreasing the need for risky procedures, such as surgical lung biopsy. Secondly, a prognostic biomarker would distinguish rapid progressors from slow progressors, which is difficult today. This study will prospectively include patients at the two largest centres in Denmark where patients are treated for IPF and has thus a good opportunity to include the majority of incident cases of IPF in Denmark. The blood levels of several promising biomarkers will be measured at baseline and during up to 5 years follow-up. Patients will also be followed up through regular clinical examination and by querying national registries to determine disease progression, mortality, healthcare utilization and selected co-morbidities. The database will be used for determination of risk factors for the outcomes listed above. Sub-group analyses are planned in respect to sex, treatment, radiologic imaging, smoking status, clinical data such as pulmonary function tests, co-morbidities (both pulmonary disease and extra-pulmonary disease), and disease severity at baseline. A research biobank with blood samples is established from the study population. This biobank, and the database of newly diagnosed IPF patients, will be used for future research in IPF. The prospectively created database will also be used for future research in IPF.
Study Type
OBSERVATIONAL
Enrollment
450
Gentofte Hospital
Hellerup, Copenhagen, Denmark
Aarhus University Hospital
Aarhus, Denmark
Disease progression or mortality
Number of patients who fulfil any of the following: disease progression or death
Time frame: 1 year
Hospitalizations
Number of respiratory and non-respiratory hospitalizations
Time frame: 1 year
Exacerbations
Number of acute exacerbations of idiopathic pulmonary fibrosis
Time frame: 1 year
Lung function tests
Reduction in diffusion capacity (DLCO) and forced vital capacity (FVC)
Time frame: 1 year
Mortality
All-cause and disease-specific mortality
Time frame: 1 year
Change in quality of life
Change in St. George Respiratory Questionnaire, symptom scores
Time frame: 1 year
Combined end-point of disease progression
Number of patients who fulfill any of the following: decrease in lung function, reduced walking distance at 6 minutes walking test, increased need for supplementary oxygen, hospitalization
Time frame: 1 year
Progression in serum/plasma biomarker levels
Increase or decrease in serum/plasma biomarker levels.
Time frame: 1 year
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