Prediction of disease severity in COPD: a deep learning approach for anomaly-based quantitative assessment of chest CT

被引:13
作者
Almeida, Silvia D. [1 ,2 ,3 ,4 ,5 ]
Norajitra, Tobias [1 ,2 ]
Lueth, Carsten T. [6 ,7 ]
Wald, Tassilo [1 ,7 ]
Weru, Vivienn [8 ]
Nolden, Marco [1 ,9 ]
Jaeger, Paul F. [6 ,7 ]
von Stackelberg, Oyunbileg [9 ,10 ]
Heussel, Claus Peter [2 ,10 ,11 ]
Weinheimer, Oliver [2 ,10 ]
Biederer, Juergen [2 ,10 ,12 ,13 ]
Kauczor, Hans-Ulrich [2 ,10 ]
Maier-Hein, Klaus [1 ,2 ,4 ,5 ,7 ,9 ]
机构
[1] German Canc Res Ctr, Div Med Image Comp, Neuenheimer Feld 280, D-69120 Heidelberg, Germany
[2] Translat Lung Res Ctr Heidelberg, Member German Lung Res Ctr DZL, Heidelberg, Germany
[3] Heidelberg Univ, Med Fac, Heidelberg, Germany
[4] Natl Ctr Tumor Dis NCT, NCT Heidelberg, Partnership DKFZ, Heidelberg, Germany
[5] Heidelberg Univ Med Ctr, Heidelberg, Germany
[6] German Canc Res Ctr, Interact Machine Learning Grp IML, Heidelberg, Germany
[7] German Canc Res Ctr, Helmholtz Imaging, Heidelberg, Germany
[8] German Canc Res Ctr, Div Biostat, Heidelberg, Germany
[9] Heidelberg Univ Hosp, Pattern Anal & Learning Grp, Radiat Oncol, Heidelberg, Germany
[10] Univ Heidelberg Hosp, Dept Diagnost & Intervent Radiol, Heidelberg, Germany
[11] Thoraxklin Univ Hosp, Diagnost & Intervent Radiol Nucl Med, Heidelberg, Germany
[12] Univ Latvia, Fac Med, Raina Bulvaris 19, LV-1586 Riga, Latvia
[13] Christian Albrechts Univ Kiel, Fac Med, D-24098 Kiel, Germany
关键词
Chronic obstructive pulmonary disease; Deep learning; Artificial intelligence; Computed tomography; QUALITY-OF-LIFE; PULMONARY-FUNCTION; RISK-FACTORS; EMPHYSEMA;
D O I
10.1007/s00330-023-10540-3
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
100231 [临床病理学]; 100902 [航空航天医学];
摘要
Objectives To quantify regional manifestations related to COPD as anomalies from a modeled distribution of normal-appearing lung on chest CT using a deep learning (DL) approach, and to assess its potential to predict disease severity.Materials and methods Paired inspiratory/expiratory CT and clinical data from COPDGene and COSYCONET cohort studies were included. COPDGene data served as training/validation/test data sets (N = 3144/786/1310) and COSYCONET as external test set (N = 446). To differentiate low-risk (healthy/minimal disease, [GOLD 0]) from COPD patients (GOLD 1-4), the self-supervised DL model learned semantic information from 50 x 50 x 50 voxel samples from segmented intact lungs. An anomaly detection approach was trained to quantify lung abnormalities related to COPD, as regional deviations. Four supervised DL models were run for comparison. The clinical and radiological predictive power of the proposed anomaly score was assessed using linear mixed effects models (LMM).Results The proposed approach achieved an area under the curve of 84.3 +/- 0.3 (p < 0.001) for COPDGene and 76.3 +/- 0.6 (p < 0.001) for COSYCONET, outperforming supervised models even when including only inspiratory CT. Anomaly scores significantly improved fitting of LMM for predicting lung function, health status, and quantitative CT features (emphysema/air trapping; p < 0.001). Higher anomaly scores were significantly associated with exacerbations for both cohorts (p < 0.001) and greater dyspnea scores for COPDGene (p < 0.001).Conclusion Quantifying heterogeneous COPD manifestations as anomaly offers advantages over supervised methods and was found to be predictive for lung function impairment and morphology deterioration.
引用
收藏
页码:4379 / 4392
页数:14
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