Aerobic and Other Exercise Training Should Be Standard of Care for IPF, Review Argues

A new review covering the benefits of exercise training in idiopathic pulmonary fibrosis (IPF) has been recently published in the journal Breathe.

ProterixBio Names Dr. Fernando Martinez of Weill Cornell to Its Scientific Advisory Board

Dr. Fernando Martinez, a clinical specialist in lung diseases such as idiopathic pulmonary fibrosis (IPF) and chronic obstructive pulmonary disease (COPD), is the newest member of the scientific and medical advisory board of ProterixBio, the company announced. His appointment as scientific and medical advisor reflects the company’s focus on solutions to improve care…

Lung Tissue from IPF Patients Shows Signs of Cell Senescence, Thought to Trigger Inflammation

University of California, San Francisco, researchers reported that markers of cellular senescence — a process preventing cells from multiplying uncontrollably — are overly abundant in cells lining lung alveoli in patients with idiopathic pulmonary fibrosis (IPF). The study, “miR-34 miRNAs Regulate Cellular Senescence in Type II Alveolar Epithelial…

Lung Fibrosis in Mice Slowed by Protein Blocking Blood Coagulation

Researchers from The Netherlands found that mice producing high levels of protein C which prevents blood coagulation, develop less severe pulmonary fibrosis; and the milder disease course is linked to lower numbers of immune cells in the lung. The study, “High endogenous activated protein C levels attenuates bleomycin-induced pulmonary fibrosis,“ published in…

Lung Remodeling Process in IPF Includes Both Traction Bronchiectasis and Honeycombing, Study Suggests

Two clinical hallmarks of patients with idiopathic pulmonary fibrosis (IPF), traction bronchiectasis and honeycombing, may be aspects of one continuous process of lung remodeling rather than distinct entities, as previously thought, according to researchers in Italy. Traction bronchiectasis refers to an irreversible dilation of bronchi, and honeycombing to the diffuse pulmonary…

Lung Fibrosis Increases Levels of Specific Surface Proteins, Suggests Disease Markers

A recent study published in the journal PLOS One, found two members of a class of proteins called surfactant proteins (SPs) at increased levels as a result of lung fibrosis and suggests that future studies could reveal the proteins, SP-A and SP-D,  as markers of disease severity. Pulmonary emphysema and idiopathic pulmonary fibrosis (IPF) are defined…

Your PF Community

Woman laying down reading

Visit the Pulmonary Fibrosis News forums to connect with others in the PF community.

View Forums