Patients with idiopathic pulmonary fibrosis (IPF) have worse outcomes if they live in poor neighborhoods, according to research presented at ATS 2021.
Gillian Goobie, MD, Human Genetics, Graduate School of Public Health, University of Pittsburgh, and colleagues sought to determine how environmental and occupational factors contribute to the development and progression of IPF. People who live in areas with high neighborhood-level disadvantage, as measured by the Area Deprivation Index, experience disparities in housing, poverty, employment, and education. These social determinants of health impact the outcome of many chronic diseases.
“Our preliminary data from our single center study at the University of Pittsburgh indicates that neighborhood-level disadvantagemay be associated with increased mortality and reduced odds of receiving a lung transplant in patients with IPF,” stated Dr. Goobie, study author.
Policies and legislation that promote more equitable environments and reduce the burden of poverty in our society may help to alleviate the disparities we see in outcomes of patients with IPF. People are more likely to develop IPF or other forms of interstitial lung disease (ILD) if they have worked in an occupation that has significant exposure to airborne materials. For example, individuals exposed to asbestos, silica, wood chippings, or numerous other materials through their work are at a higher risk for development of ILD in comparison to individuals without those exposures. We also know that smoking is a very important risk factor that contributes to the development of IPF in many patients, as well as exposure to air pollution.
“I think there are substantial real-world implications of this research. With a disease like IPF, which has a very high mortality, we are more able to demonstrate the substantial impact that these neighborhood-level factors can have on survival and transplant outcomes. I was surprised that we were able to find a significant impact of neighborhood-level disadvantage on survival in our relatively small cohort of patients with IPF. I am looking forward to validating these results in a larger and more diverse population of patients with IPF and other forms of fibrotic ILD,” said Dr. Goobie.