Idiopathic pulmonary fibrosis (IPF), the most common and severe form of pulmonary fibrosis (PF), is increasing in prevalence, and has a median survival of 3-5 years. Recent studies have finally demonstrated that anti- fibrotic therapy can reduce the rate of decline in lung function, IPF remains a relentlessly progressive condition in part due to the advanced stages of PF at the time of presentation. There is also evidence that anti-fibrotic therapy reduces progression in patients with less severe disease; which suggests that early detection may improve outcomes. Dr. Putman?s work has shown that the early stages of PF are detectable, that radiologic progression is relatively frequent, is correlated with genetic factors seen in IPF patients (e.g. MUC5B genotype), and is associated with an accelerated rate of lung function decline and an increased risk of death. Although much work has been done to demonstrate that imaging analyses can detect patterns that help to predict adverse outcomes in IPF, it is unclear what radiologic characteristics of ILA best predict accelerated progression and mortality. Additionally, numerous studies have demonstrated that mean telomere length (MTL), and variants in multiple genes controlling MTL are associated with IPF and reduced survival, the role of these factors in determining the progression and mortality associated with ILA is not known. In the first aim, Dr. Putman will identify the radiologic factors, both qualitative and quantitative, that are most associated with the progression of PF, and relate these findings to clinical outcomes. In the second aim she will explore the relationship between reduced MTL and the progression of early stage PF. Finally, in the third aim, using whole genome sequencing data, she will explore the relationship between genetic mutations in the telomerase pathway and progression of early stage pulmonary fibrosis. This work will be performed in the Division of Pulmonary and Critical Care Medicine, at Brigham and Women?s Hospital (BWH), a core teaching hospital of Harvard Medical School. Dr. Putman will perform this work under the mentorship of Dr. Hunninghake, an expert in the field of early pulmonary fibrosis and Dr. Silverman, an expert in COPD genetics. With the guidance of her mentors and scientific advisory committee, Dr. Putman has developed a comprehensive five year training program to develop the skills needed to become an independent investigator with expertise in complex genetic analyses and their integration with image characterization. Dr. Putman is dedicated to a career in academic medicine. Her goal is to become a clinician-scientist using the skills gained during this award to better our understanding of the biologic processes that lead to PF occurrence and progression. She plans to use the knowledge gained from this award to study the downstream consequences of decreased MTL; with the ultimate goal of improving care and outcomes in patients with PF.

Public Health Relevance

Idiopathic pulmonary fibrosis (IPF) is a progressive disease characterized by scarring in the lungs and carries a prognosis worse than many cancers. With the advent of anti-fibrotic therapy, which slows disease progression, it has become more important to identify which patients will progress from early stage disease. This proposal aims to improve our understanding of the radiologic, biologic, and genetic factors that predict disease progression. The results of this work will help to identify which patients are at higher risk for accelerated disease progression and would benefit from the early initiation of anti-fibrotic therapy.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08HL140087-03
Application #
9843715
Study Section
NHLBI Mentored Patient-Oriented Research Review Committee (MPOR)
Program Officer
Kalantari, Roya
Project Start
2018-01-19
Project End
2022-12-31
Budget Start
2020-01-01
Budget End
2020-12-31
Support Year
3
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
030811269
City
Boston
State
MA
Country
United States
Zip Code