Role of Genetics in Idiopathic Pulmonary Fibrosis (IPF)

Purpose

The purpose of this study is to investigate inherited genetic factors that play a role in the development of familial pulmonary fibrosis and to identify a group of genes that predispose individuals to develop pulmonary fibrosis. Finding the genes that cause pulmonary fibrosis is the first step at developing better methods for early diagnosis and improved treatment for pulmonary fibrosis. The overall hypothesis is that inherited genetic factors predispose individuals to develop pulmonary fibrosis.

Conditions

  • Idiopathic Pulmonary Fibrosis
  • Familial Pulmonary Fibrosis
  • Idiopathic Interstitial Pneumonia
  • Familial Interstitial Pneumonia

Eligibility

Eligible Ages
All ages
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Two or more family members with a clinical diagnosis of Idiopathic Pulmonary Fibrosis (IPF) or Idiopathic Interstitial Pneumonia (IIP) - Additional family members may be eligible to participate if two family members are suspected of or diagnosed as having Idiopathic Pulmonary Fibrosis (IPF) or Idiopathic Interstitial Pneumonia (IIP)

Exclusion Criteria

  • Individuals whose pulmonary fibrosis is due to a known cause rather than idiopathic - Individuals whose pulmonary fibrosis is due to a broader genetic syndrome

Study Design

Phase
Study Type
Observational
Observational Model
Family-Based
Time Perspective
Cross-Sectional

Recruiting Locations

Vanderbilt University
Nashville, Tennessee 37232
Contact:
Cheryl Markin, MT
888-898-1550
cheryl.markin@vanderbilt.edu

More Details

Status
Recruiting
Sponsor
National Jewish Health

Study Contact

Julie Powers, MHS
303-724-6539
julia.powers@ucdenver.edu

Detailed Description

Familial Pulmonary Fibrosis (FPF) is a sub-category of the idiopathic interstitial pneumonias (IIPs). IIPs are progressive lung conditions, with limited treatment options and unknown etiology. Though the IIPs have been associated with both genetic risk factors and environmental exposures, the molecular mechanism underlying disease progression remain poorly understood. This investigation seeks to identify a group of genetic loci that play a role in the development of familial interstitial pneumonia (FIP) or FPF, where 2 or more cases of IIP are seen within a family.