Identification of a conserved sequence of disease progression in Idiopathic Pulmonary Fibrosis
We identified a conserved sequential decline in lung function in IPF, which has important implications for the design of clinical trials. The DPM provides a powerful framework to investigate the clinical and/or biological processes that initiate and propagate IPF.
Authors
- Jonathan A. Kropski (ORCID: https://orcid.org/0000-0002-8923-1344)
- Peng Wu (ORCID: https://orcid.org/0000-0003-2026-4102)
- Margaret L. Salisbury (ORCID: https://orcid.org/0000-0001-8217-6955)
- Timothy S. Blackwell (ORCID: https://orcid.org/0000-0002-0337-7052)
- Adam Guttentag
- Melanie Quintana
- Xiang Huang
Institutions
- Vanderbilt University (US)
- University of Michigan (US)
- Berry & Associates (United States) (US)
- Nashville VA Medical Center (US)
- Michigan Medicine (US)
- Department of Veterans Affairs (AU)
- Vanderbilt University Medical Center (US)
Publication Details
- Journal
- American Journal of Respiratory and Critical Care Medicine
- Published
- 2026-02-13
- DOI
- https://doi.org/10.1093/ajrccm/aamag075
- Primary Topic
- Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Type
- article
- Field-Weighted Citation Impact
- 0.00