Raghunath Sushravya, Rajagopalan Srinivasan, Karwoski Ronald A, Maldonado Fabien, Peikert Tobias, Moua Teng, Ryu Jay H, Bartholmai Brian J, Robb Richard A
Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota, United States of America.
Division of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, Minnesota, United States of America.
PLoS One. 2014 Mar 27;9(3):e93229. doi: 10.1371/journal.pone.0093229. eCollection 2014.
Diffuse parenchymal lung diseases (DPLDs) are characterized by widespread pathological changes within the pulmonary tissue that impair the elasticity and gas exchange properties of the lungs. Clinical-radiological diagnosis of these diseases remains challenging and their clinical course is characterized by variable disease progression. These challenges have hindered the introduction of robust objective biomarkers for patient-specific prediction based on specific phenotypes in clinical practice for patients with DPLD. Therefore, strategies facilitating individualized clinical management, staging and identification of specific phenotypes linked to clinical disease outcomes or therapeutic responses are urgently needed. A classification schema consistently reflecting the radiological, clinical (lung function and clinical outcomes) and pathological features of a disease represents a critical need in modern pulmonary medicine. Herein, we report a quantitative stratification paradigm to identify subsets of DPLD patients with characteristic radiologic patterns in an unsupervised manner and demonstrate significant correlation of these self-organized disease groups with clinically accepted surrogate endpoints. The proposed consistent and reproducible technique could potentially transform diagnostic staging, clinical management and prognostication of DPLD patients as well as facilitate patient selection for clinical trials beyond the ability of current radiological tools. In addition, the sequential quantitative stratification of the type and extent of parenchymal process may allow standardized and objective monitoring of disease, early assessment of treatment response and mortality prediction for DPLD patients.
弥漫性肺实质疾病(DPLD)的特征是肺组织内广泛的病理变化,这些变化损害了肺的弹性和气体交换特性。这些疾病的临床放射学诊断仍然具有挑战性,其临床病程的特点是疾病进展多变。这些挑战阻碍了在临床实践中为DPLD患者基于特定表型引入强大的客观生物标志物以进行个体化预测。因此,迫切需要有助于个体化临床管理、分期以及识别与临床疾病结局或治疗反应相关的特定表型的策略。一种始终如一地反映疾病的放射学、临床(肺功能和临床结局)和病理特征的分类模式是现代肺病学的迫切需求。在此,我们报告一种定量分层范式,以无监督方式识别具有特征性放射学模式的DPLD患者亚组,并证明这些自组织疾病组与临床认可的替代终点之间存在显著相关性。所提出的一致且可重复的技术有可能改变DPLD患者的诊断分期、临床管理和预后,并且除了当前放射学工具的能力之外,还能促进临床试验中的患者选择。此外,对实质病变类型和范围的序贯定量分层可能允许对DPLD患者的疾病进行标准化和客观监测、早期评估治疗反应以及预测死亡率。