Department of Radiology, University of Michigan, Ann Arbor, MI 48109, USA.
Antwerp Surgical Training, Anatomy and Research Centre (ASTARC), Faculty of Medicine and Health Sciences, University of Antwerp, Wilrijk, 2610 Antwerp, Belgium.
Cells. 2022 Feb 16;11(4):699. doi: 10.3390/cells11040699.
Chronic rejection of lung allografts has two major subtypes, bronchiolitis obliterans syndrome (BOS) and restrictive allograft syndrome (RAS), which present radiologically either as air trapping with small airways disease or with persistent pleuroparenchymal opacities. Parametric response mapping (PRM), a computed tomography (CT) methodology, has been demonstrated as an objective readout of BOS and RAS and bears prognostic importance, but has yet to be correlated to biological measures. Using a topological technique, we evaluate the distribution and arrangement of PRM-derived classifications of pulmonary abnormalities from lung transplant recipients undergoing redo-transplantation for end-stage BOS (N = 6) or RAS (N = 6). Topological metrics were determined from each PRM classification and compared to structural and biological markers determined from microCT and histopathology of lung core samples. Whole-lung measurements of PRM-defined functional small airways disease (fSAD), which serves as a readout of BOS, were significantly elevated in BOS versus RAS patients ( = 0.01). At the core-level, PRM-defined parenchymal disease, a potential readout of RAS, was found to correlate to neutrophil and collagen I levels ( < 0.05). We demonstrate the relationship of structural and biological markers to the CT-based distribution and arrangement of PRM-derived readouts of BOS and RAS.
慢性肺移植排斥反应有两种主要亚型,即细支气管炎性闭塞综合征(BOS)和限制型移植物综合征(RAS),这两种疾病在影像学上表现为小气道疾病导致的空气潴留或持续性胸膜实质混浊。参数反应映射(PRM)是一种计算机断层扫描(CT)方法,已被证明是 BOS 和 RAS 的客观指标,并具有预后意义,但尚未与生物学指标相关联。本研究采用拓扑学技术,评估了 6 例因终末期 BOS(BOS)和 6 例因 RAS 而接受再次移植的肺移植受者的 PRM 衍生的肺异常分类的分布和排列。从每个 PRM 分类中确定拓扑学指标,并与通过微 CT 和肺核心样本的组织病理学确定的结构和生物学标志物进行比较。作为 BOS 读出的 PRM 定义的功能性小气道疾病(fSAD)的全肺测量值在 BOS 患者中显著高于 RAS 患者(=0.01)。在核心水平,PRM 定义的实质疾病,可能是 RAS 的读出,与中性粒细胞和胶原 I 水平相关(<0.05)。我们证明了结构和生物学标志物与基于 CT 的 PRM 衍生的 BOS 和 RAS 读出的分布和排列之间的关系。