医学
特发性肺纤维化
表型
肺
间质性肺病
病理
纤维化
免疫学
肺纤维化
人口
内科学
生物
基因
生物化学
环境卫生
作者
Yoshikazu Inoue,Robert J. Kaner,Julien Guiot,Toby M. Maher,Sara Tomassetti,Sergey Moiseev,Masataka Kuwana,Kevin K. Brown
出处
期刊:Chest
[Elsevier BV]
日期:2020-04-05
卷期号:158 (2): 646-659
被引量:116
标识
DOI:10.1016/j.chest.2020.03.037
摘要
Biomarkers have the potential to become central to the clinical evaluation and monitoring of patients with chronic fibrosing interstitial lung diseases (ILDs) with a progressive phenotype. Here we summarize the current understanding of putative serum, BAL fluid, and genetic biomarkers in this setting, according to their hypothesized pathobiologic mechanisms: evidence of epithelial cell dysfunction (eg, Krebs von den Lungen-6 antigen), fibroblast proliferation and extracellular matrix production or turnover (eg, matrix metalloproteinase-1), or immune dysregulation (eg, CC chemokine ligand 18). While most of the available data come from idiopathic pulmonary fibrosis (IPF), the prototypic progressive fibrosing ILD, data are available in the broader patient population of chronic fibrosing ILDs. A number of these biomarkers show promise, however, none have been validated. In this review article, we assess both the status of proposed biomarkers for chronic fibrosing lung diseases with a progressive phenotype in predicting disease risk or predisposition, diagnosis, prognosis, and treatment response and provide a direct comparison between IPF and other chronic fibrotic ILDs. We also reflect on the current clinical usefulness and future direction of research for biomarkers in the setting of chronic fibrosing ILDs with a progressive phenotype.
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