Update in diffuse parenchymal lung disease, 2013.

Abstract:

:The period covered by this update can be considered as the most exciting period in idiopathic pulmonary fibrosis (IPF) research. It started with the identification of genetic variants that are associated with IPF in the majority of patients and continued with discovery of molecular and genetic biomarkers that predict distinct clinical presentations of patients with IPF and potential new biological mechanisms. More importantly, the period ends with the publication of two groundbreaking studies that confirmed that two drugs, pirfenidone and nintedanib, slowed disease progression, leading to a historic approval by the FDA. In this update, we describe these key advances, their scientific and significant clinical implications, and future directions.

authors

Rosas IO,Kaminski N

doi

10.1164/rccm.201405-0856UP

subject

Has Abstract

pub_date

2015-02-01 00:00:00

pages

270-4

issue

3

eissn

1073-449X

issn

1535-4970

journal_volume

191

pub_type

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