Facts and promises on lung biomarkers in interstitial lung diseases

被引:16
|
作者
Campo, Ilaria [1 ]
Zorzetto, Michele [1 ]
Bonella, Francesco [2 ]
机构
[1] Fdn IRCCS Policlin San Matteo, SC Pneumol, I-27100 Pavia, Italy
[2] Ruhrlandklin Univ Hosp, Interstitial & Rare Lung Dis Unit, D-45239 Essen, Germany
关键词
circulating biomarkers; epigenetics; genes; genome-wide analysis; interstitial lung disease; lung fibrosis; miRNAs; IDIOPATHIC PULMONARY-FIBROSIS; BRONCHOALVEOLAR LAVAGE FLUID; SURFACTANT PROTEIN-D; MUC5B PROMOTER POLYMORPHISM; TISSUE GROWTH-FACTOR; MATRIX-METALLOPROTEINASE; 7; EARLY SYSTEMIC-SCLEROSIS; CYTOKERATIN; 19; FRAGMENT; C-REACTIVE PROTEIN; REGULATORY T-CELLS;
D O I
10.1586/17476348.2015.1062367
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Interstitial lung diseases (ILDs) are a heterogeneous group of >100 pulmonary disorders. ILDs are characterized by an irreversible architectural distortion and impaired gas exchange; however, there is great variability in the clinical course. ILD diagnosis requires a combination of clinical data, radiological imaging and histological findings (when a lung biopsy is required). At the same time, successful management of ILD patients strictly depends on an accurate and confident diagnosis. In this context, the detection of reliable biomarkers able to identify ILD subtypes, avoiding lung biopsy, as well as the capacity to stratify patients and predict over time the disease course, has become a primary aim for all research studies in this field.
引用
收藏
页码:437 / 457
页数:21
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