医学
观察研究
特发性肺纤维化
潜在类模型
肺纤维化
内科学
重症监护医学
纤维化
肺
统计
数学
作者
Manoj V. Maddali,A. R. Moore,Pratik Sinha,Chad A. Newton,John S. Kim,Ayodeji Adegunsoye,Shwu‐Fan Ma,Mary E. Strek,Ching‐Hsien Chen,A. Linderholm,Rachel L. Zemans,Bethany B. Moore,Paul J. Wolters,Fernando J. Martínez,Angela J. Rogers,Rishi Raj,Imre Noth,Justin M. Oldham
标识
DOI：10.1164/rccm.202402-0339oc
摘要
Idiopathic pulmonary fibrosis (IPF) causes irreversible fibrosis of the lung parenchyma. While antifibrotic therapy can slow IPF progression, treatment response is variable. There exists a critical need to develop a precision medicine approach to IPF.
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