Precision Medicine: The New Frontier in Idiopathic Pulmonary Fibrosis

被引:54
作者
Brownell, Robert [1 ]
Kaminski, Naftali [2 ]
Woodruff, Prescott G. [1 ]
Bradford, Williamson Z. [3 ]
Richeldi, Luca [4 ,5 ]
Martinez, Fernando J. [6 ]
Collard, Harold R. [1 ]
机构
[1] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[2] Yale Univ, Sch Med, Dept Med, New Haven, CT 06510 USA
[3] WZB Consulting, Wilson, WY USA
[4] Univ Southampton, Natl Inst Hlth Res, Southampton Resp Biomed Res Unit, Southampton, Hants, England
[5] Univ Southampton, Clin & Expt Sci, Southampton, Hants, England
[6] Weill Cornell Univ, Sch Med, Dept Med, New York, NY USA
关键词
idiopathic pulmonary fibrosis; stratified medicine; precision medicine; endotypes; biological markers; INTERSTITIAL LUNG-DISEASE; SURFACTANT PROTEIN-A; MUC5B PROMOTER POLYMORPHISM; TO-SEVERE ASTHMA; GASTROESOPHAGEAL-REFLUX; BLOOD BIOMARKERS; N-ACETYLCYSTEINE; GENE-EXPRESSION; PHASE-3; TRIAL; V COLLAGEN;
D O I
10.1164/rccm.201601-0169CI
中图分类号
R4 [临床医学];
学科分类号
100218 [急诊医学];
摘要
Precision medicine is defined by the National Institute of Health's Precision Medicine Initiative Working Group as an approach to disease treatment that takes into account individual variability in genes, environment, and lifestyle. There has been increased interest in applying the concept of precision medicine to idiopathic pulmonary fibrosis, in particular to search for genetic and molecular biomarker-based profiles (so called endotypes) that identify mechanistically distinct disease subgroups. The relevance of precision medicine to idiopathic pulmonary fibrosis is yet to be established, but we believe that it holds great promise to provide targeted and highly effective therapies to patients. In this manuscript, we describe the field's nascent efforts in genetic/molecular endotype identification and how environmental and behavioral subgroups may also be relevant to disease management.
引用
收藏
页码:1213 / 1218
页数:6
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