Bell Alexander J, Pal Ravi, Labaki Wassim W, Hoff Benjamin A, Wang Jennifer M, Murray Susan, Kazerooni Ella A, Galban Stefanie, Lynch David A, Humphries Stephen M, Martinez Fernando J, Hatt Charles R, Han MeiLan K, Ram Sundaresh, Galban Craig J
Department of Radiology, University of Michigan, Ann Arbor, MI, United States.
Department of Internal Medicine, Division of Pulmonary and Critical Care Medicine, University of Michigan, Ann Arbor, MI, United States.
medRxiv. 2023 Nov 20:2023.05.26.23290532. doi: 10.1101/2023.05.26.23290532.
Small airways disease (SAD) is a major cause of airflow obstruction in COPD patients, and has been identified as a precursor to emphysema. Although the amount of SAD in the lungs can be quantified using our Parametric Response Mapping (PRM) approach, the full breadth of this readout as a measure of emphysema and COPD progression has yet to be explored. We evaluated topological features of PRM-derived normal parenchyma and SAD as surrogates of emphysema and predictors of spirometric decline.
PRM metrics of normal lung (PRM) and functional SAD (PRM) were generated from CT scans collected as part of the COPDGene study (n=8956). Volume density (V) and Euler-Poincaré Characteristic (χ) image maps, measures of the extent and coalescence of pocket formations (i.e., topologies), respectively, were determined for both PRM and PRM. Association with COPD severity, emphysema, and spirometric measures were assessed via multivariable regression models. Readouts were evaluated as inputs for predicting FEV decline using a machine learning model.
Multivariable cross-sectional analysis of COPD subjects showed that V and χ measures for PRM and PRM were independently associated with the amount of emphysema. Readouts χ (β of 0.106, p<0.001) and V (β of 0.065, p=0.004) were also independently associated with FEV% predicted. The machine learning model using PRM topologies as inputs predicted FEV decline over five years with an AUC of 0.69.
We demonstrated that V and χ of fSAD and Norm have independent value when associated with lung function and emphysema. In addition, we demonstrated that these readouts are predictive of spirometric decline when used as inputs in a ML model. Our topological PRM approach using PRM and PRM may show promise as an early indicator of emphysema onset and COPD progression.
小气道疾病(SAD)是慢性阻塞性肺疾病(COPD)患者气流受限的主要原因,并且已被确定为肺气肿的先兆。尽管可使用我们的参数反应映射(PRM)方法对肺内SAD的量进行量化,但作为肺气肿和COPD进展指标的这一读数的全部意义尚未得到探索。我们评估了PRM衍生的正常实质和SAD的拓扑特征,将其作为肺气肿的替代指标和肺功能下降的预测指标。
正常肺(PRM)和功能性SAD(PRM)的PRM指标由作为COPDGene研究一部分收集的CT扫描生成(n = 8956)。分别为PRM和PRM确定了体积密度(V)和欧拉-庞加莱特征(χ)图像图谱,它们分别是腔隙形成(即拓扑结构)范围和合并情况的测量指标。通过多变量回归模型评估与COPD严重程度、肺气肿和肺功能测量指标的相关性。使用机器学习模型将读数评估为预测第一秒用力呼气容积(FEV)下降的输入指标。
对COPD受试者的多变量横断面分析表明,PRM和PRM的V和χ测量值与肺气肿的量独立相关。读数χ(β为0.106,p<0.001)和V(β为0.065,p = 0.004)也与预测的FEV%独立相关。使用PRM拓扑结构作为输入的机器学习模型预测了五年内的FEV下降,曲线下面积(AUC)为0.69。
我们证明,fSAD和Norm的V和χ与肺功能和肺气肿相关时具有独立价值。此外,我们证明,当在机器学习模型中用作输入时,这些读数可预测肺功能下降。我们使用PRM和PRM的拓扑PRM方法可能有望作为肺气肿发病和COPD进展的早期指标。