Idiopathic Pulmonary Fibrosis (IPF)
Conditions
Keywords
Idiopathic pulmonary fibrosis, pulmonary macrophages, alveolar macrophages, vitamin D, Soluble CD163, Soluble CD206
Brief summary
The goal of this observational study is to gain deeper insights into human macrophages and vitamin D, and their interplay, within Idiopathic Pulmonary Fibrosis (IPF). The overall questions, it aims to answer, are the following: Do IPF patients suffer from systemic and local (pulmonary) insufficient levels of vitamin D? Do IPF patients suffer from pro-fibrotic and pro-inflammatory pulmonary macrophages?
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* A clinical diagnosis of IPF, non-IPF ILD or lung cancer * A signed informed consent
Exclusion criteria
* Do not speak Danish/Do not understand Danish
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Vitamin D status | At enrollment | Significant change in vitamin D levels in systemic (blood) and local (pulmonary) metabolism. |
| Pulmonary macrophages | At enrollment | Significant change in alveolar macrophage phenotype |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Biomarker levels in blood and BAL samples | At enrollment | Significant change in levels of macrophage and inflammatory/fibrotic biomarkers |
Countries
Denmark