Idiopathic Pulmonary Fibrosis, a Disease Initiated by Mucociliary Dysfunction
University of Colorado, Denver
Summary
This study seeks to screen first degree family members of people with Idiopathic Pulmonary Fibrosis (IPF) for the earliest signs of lung fibrosis.
Description
The purpose of this study is to explore genetic factors associated with the development of pulmonary fibrosis. The investigators aim is to identify and explore genetic loci that affect development of pulmonary fibrosis and also explore related environmental exposures. Idiopathic pulmonary fibrosis (IPF) is one of the interstitial lung diseases under the broader umbrella of idiopathic interstitial pneumonias (IIP). The investigators hypothesize that inherited genetic factors are associated with pulmonary fibrosis. To investigate the genetics of pulmonary fibrosis, the investigators plan to enro…
Eligibility
- Age range
- 18+ years
- Sex
- All
- Healthy volunteers
- Yes
Inclusion Criteria: * Age at least 18 years old * Family member diagnosed with IPF Exclusion Criteria: \- No family member with IPF
Interventions
- OtherBlood draw
Blood draw
- OtherQuestionnaire
Pulmonary Fibrosis Questionnaire
Location
- University of Colorado Anschutz Medical CampusAurora, Colorado