Perlikos Fotis, Hillas Giorgos, Loukides Stelios
Smolika 2 16673, Athens, Greece.
Curr Top Med Chem. 2016;16(14):1582-6. doi: 10.2174/1568026616666150930120803.
Asthma is a chronic inflammatory airways disorder mainly characterized by heterogeneity. A phenotype is defined as a group of patients that present similar clinically observable characteristics, without establishing a direct etiologic relationship with a distinct pathophysiologic mechanism. An endotype, on the other hand, describes a subgroup that shares the same pathophysiologic processes that lead to the development, the progression and the presentation of a disease. A biomarker has been defined as a characteristic that is objectively measured and evaluated as an indicator of normal biological processes, pathogenic processes or pharmacologic responses to a therapeutic intervention. Several inflammatory phenotypes have been identified by the use of biomarkers. Most of them are based on the predominant type of cells in different biological fluids with sputum to be remained the most representative one. Eosinophilia represents the major characteristic of what we called classic atopic asthma. This particular phenotype usually responds well to corticosteroids, except for a small subgroup of severe asthma where even in the presence of eosinophils the ICS seem to have a less responsive role. Neutrophilic phenotype driven by the presence of neutrophils shows inadequate response to corticosteroid treatment, even in mild asthma. The major approach in order to define an endotype is driven by three main parameters. The statistical clustering approach, use of advanced statistical mathematics to create distinct patient clusters, the specific targeted immune therapies and finally the application of omics' approach. Both phenotypes and endotypes are trying to clarify mechanisms and processes that driven the complexity of asthma. Both concepts could identify approaches which could establish new targeted to specific biomarkers treatment therapies/strategies.
哮喘是一种慢性炎症性气道疾病,主要特征为异质性。一种表型被定义为一组具有相似临床可观察特征的患者,而未与特定病理生理机制建立直接病因关系。另一方面,一种内型描述的是共享导致疾病发生、发展和表现的相同病理生理过程的亚组。生物标志物被定义为一种可客观测量和评估的特征,作为正常生物过程、致病过程或对治疗干预的药理反应的指标。通过使用生物标志物已确定了几种炎症表型。其中大多数基于不同生物体液中占主导地位的细胞类型,痰液仍是最具代表性的一种。嗜酸性粒细胞增多是我们所称的经典特应性哮喘的主要特征。这种特定表型通常对皮质类固醇反应良好,但有一小部分严重哮喘患者除外,即使存在嗜酸性粒细胞,吸入性糖皮质激素(ICS)似乎也作用较小。由中性粒细胞的存在驱动的中性粒细胞表型对皮质类固醇治疗反应不足,即使在轻度哮喘中也是如此。定义内型的主要方法由三个主要参数驱动。统计聚类方法,即使用先进的统计数学创建不同的患者聚类,特定的靶向免疫疗法,以及最后组学方法的应用。表型和内型都试图阐明驱动哮喘复杂性的机制和过程。这两个概念都可以确定能够建立针对特定生物标志物的新治疗疗法/策略的方法。