Idiopathic pulmonary fibrosis (IPF) is a progressive fibrotic disease of the peripheral lung parenchyma that affects ~0.5% of older adults in the US and carries a median survival time of only 3.8 years. While pirfenidone and nintedanib slow the decline of lung function in IPF, neither drug reverses fibrosis or prevents the ongoing alveolar epithelial cell injury that leads to fibrosis in IPF. The identification of interventions that prevent alveolar epithelial cell injury in IPF would have a paradigm-shifting impact. A recent novel hypothesis suggests that ?tractional? injury in the periphery of the lung may be responsible for the development of IPF. Our central hypothesis is that obstructive sleep apnea (OSA), which affects up to 88% of adults with IPF, is a prevalent cause of recurrent peripheral tractional stress in the lung that leads to alveolar epithelial cell injury and, in susceptible individuals, lung fibrosis. We believe that the Meller maneuvers induced during obstructive apneas and hypopneas lead to stretch and injury alveolar epithelial cells, contributing to fibrosis in susceptible adults over the course of 10-20 years. In mice, inspiratory resistive loading (a model of obstructive hypopnea) induces alveolar epithelial cell injury and results in increased alveolar-capillary membrane permeability. In humans, we and others have shown that adults with OSA have higher circulating levels of surfactant protein-A and Krebs von den Lungen-6, markers of alveolar epithelial cell injury, and higher serum matrix metalloproteinase-7 levels, a marker of extracellular matrix remodeling, suggesting that subclinical alveolar epithelial cell injury and extracellular matrix remodeling occurs in OSA in otherwise healthy adults. Alveolar epithelial and endothelial injury is also detectable by measurement of serum surfactant protein-D, and angiopoetin-2, respectively. In IPF, alveolar epithelial cell injury is detectable by elevations in some of these markers, and matrix metalloproteinase-7 levels are a key diagnostic and prognostic biomarker in IPF. We propose to establish OSA as a contributor to alveolar epithelial cell injury in adults with and without IPF, and to obtain data that will inform and justify a phase 2 clinical trial of continuous positive airway pressure (CPAP) to improve outcomes in adults with IPF and OSA. We will investigate associations between OSA and biomarkers of alveolar epithelial & endothelial cell injury and extracellular matrix remodeling a multi-ethnic population- based cohort of adults who underwent home polysomnography in 2010-2012. We will also investigate whether treatment with CPAP is associated with reductions in serum markers of alveolar epithelial cell injury and extracellular matrix remodeling in adults with OSA both with and without IPF, including measurement of CPAP- induced changes in the proteome of bronchoalveolar lavage fluid in adults with IPF. Our study will provide strong evidence for or against a pathogenic role of OSA in IPF, and is likely to provide critical data that we will use to design a phase 2 trial with a high likelihood of successfully identifying a therapeutic effect of CPAP in IPF if one exists.

Public Health Relevance

Idiopathic pulmonary fibrosis is a fatal disease of unknown cause characterized by progressive scarring of the walls of the air sacs. We believe that obstructive sleep apnea is a major and unrecognized cause of idiopathic pulmonary fibrosis. Our study will test the hypothesis that sleep apnea leads to injury of the walls of the air sacs and that treatment of sleep apnea helps to prevent this injury. The results of our study will lead to a large clinical trial to test whether treatment of sleep apnea helps improve the outcomes of adults suffering from idiopathic pulmonary fibrosis.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
1R01HL137234-01A1
Application #
9463124
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Reineck, Lora A
Project Start
2018-01-15
Project End
2021-12-31
Budget Start
2018-01-15
Budget End
2018-12-31
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032