Three-Dimensional Multiscale Fuzzy Entropy: Validation and Application to Idiopathic Pulmonary Fibrosis

被引:6
作者
Gaudencio, Andreia Sofia F. [1 ]
Vaz, Pedro G. [1 ]
Hilal, Mirvana [2 ]
Cardoso, Joao M. [1 ]
Mahe, Guillaume [3 ]
Lederlin, Mathieu [3 ]
Humeau-Heurtier, Anne [2 ]
机构
[1] Univ Coimbra, Dept Phys, LIBPhys UC, P-3004516 Coimbra, Portugal
[2] Univ Angers, LARIS Lab Angevin Rech Ingn Syst, F-49000 Angers, France
[3] Univ Hosp Rennes, F-35000 Rennes, France
关键词
Entropy; Lung; Diseases; Three-dimensional displays; Biomedical measurement; Computed tomography; Informatics; CT scan; fuzzy entropy; idiopathic pulmonary fibrosis; multiscale analysis; noise signals; TEXTURE ANALYSIS; APPROXIMATE ENTROPY; CLASSIFICATION; IRREGULARITY; DIAGNOSIS; APEN;
D O I
10.1109/JBHI.2020.2986210
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Idiopathic Pulmonary Fibrosis (IPF) is a chronic, severe, and progressive lung disease with short life expectancy. Based on information theory and entropy measurement, a three-dimensional multiscale fuzzy entropy (MFE3D) algorithm is proposed to identify IPF patients from their computed tomography (CT) volumetric data. First, the validation of the algorithm was performed by analyzing several volumetric synthetic noises (white, blue, brown, and pink), MIX(p) processes-based volumes, and texture-based volumes. The entropy values obtained by MFE3D were consistent with the values obtained using the one, and two-dimensional versions, validating its use in biomedical data. Hence, MFE3D was applied to CT scans to identify the existence of IPF within two different groups, one of healthy subjects (26) and another of IPF patients (26). Statistical differences were found (p < 0.05) between the entropy values of each group in 5 scale factors out of 10. These results demonstrate that MFE(3D)could be an interesting metric to identify IPF in CT scans.
引用
收藏
页码:100 / 107
页数:8
相关论文
共 50 条
[41]   Automated Quantitative Computed Tomography Versus Visual Computed Tomography Scoring in Idiopathic Pulmonary Fibrosis: Validation Against Pulmonary Function [J].
Jacob, Joseph ;
Bartholmai, Brian J. ;
Rajagopalan, Srinivasan ;
Kokosi, Maria ;
Nair, Arjun ;
Karwoski, Ronald ;
Raghunath, Sushravya M. ;
Walsh, Simon L. F. ;
Wells, Athol U. ;
Hansell, David M. .
JOURNAL OF THORACIC IMAGING, 2016, 31 (05) :304-311
[42]   Identification and validation of chemokine system-related genes in idiopathic pulmonary fibrosis [J].
Zhao, Tianming ;
Wu, Xu ;
Zhao, Xuelei ;
Yao, Kecheng ;
Li, Xiaojuan ;
Ni, Jixiang .
FRONTIERS IN IMMUNOLOGY, 2023, 14
[43]   Integration and Application of Clinical Practice Guidelines for the Diagnosis of Idiopathic Pulmonary Fibrosis and Fibrotic Hypersensitivity Pneumonitis [J].
Marinescu, Daniel-Costin ;
Raghu, Ganesh ;
Remy-Jardin, Martine ;
Travis, William D. ;
Adegunsoye, Ayodeji ;
Beasley, Mary Beth ;
Chung, Jonathan H. ;
Churg, Andrew ;
Cottin, Vincent ;
Egashira, Ryoko ;
Perez, Evans R. Fernandez ;
Inoue, Yoshikazu ;
Johannson, Kerri A. ;
Kazerooni, Ella A. ;
Khor, Yet H. ;
Lynch, David A. ;
Muller, Nestor L. ;
Myers, Jeffrey L. ;
Nicholson, Andrew G. ;
Rajan, Sujeet ;
Saito-Koyama, Ryoko ;
Troy, Lauren ;
Walsh, Simon L. F. ;
Wells, Athol U. ;
Wijsenbeek, Marlies S. ;
Wright, Joanne L. ;
Ryerson, Christopher J. .
CHEST, 2022, 162 (03) :614-629
[44]   Three-dimensional Airway Tree Architecture and Pulmonary Function [J].
Pu, Jiantao ;
Leader, Joseph K. ;
Meng, Xin ;
Whiting, Bruce ;
Wilson, David ;
Sciurba, Frank C. ;
Reilly, John J. ;
Bigbee, William L. ;
Siegfried, Jill ;
Gur, David .
ACADEMIC RADIOLOGY, 2012, 19 (11) :1395-1401
[45]   Development and Validation of a Novel Gene Signature for Predicting the Prognosis of Idiopathic Pulmonary Fibrosis Based on Three Epithelial-Mesenchymal Transition and Immune-Related Genes [J].
Zheng, Jiafeng ;
Dong, Hanquan ;
Zhang, Tongqiang ;
Ning, Jing ;
Xu, Yongsheng ;
Cai, Chunquan .
FRONTIERS IN GENETICS, 2022, 13
[46]   A potential three-gene-based diagnostic signature for idiopathic pulmonary fibrosis [J].
Wu, Yi ;
Zhong, Lin ;
Qiu, Li ;
Dong, Liqun ;
Yang, Lin ;
Chen, Lina .
FRONTIERS IN GENETICS, 2023, 13
[47]   Derivation and validation of a simple multidimensional index incorporating exercise capacity parameters for survival prediction in idiopathic pulmonary fibrosis [J].
Chandel, Abhimanyu ;
Pastre, Jean ;
Valery, Solene ;
King, Christopher S. ;
Nathan, Steven D. .
THORAX, 2023, 78 (04) :368-375
[48]   Factor analysis identifies three separate symptom clusters in idiopathic pulmonary fibrosis [J].
Seppala, Severi ;
Rajala, Kaisa ;
Lehto, Juho Tuomas ;
Sutinen, Eva ;
Makitalo, Laura ;
Kautiainen, Hannu ;
Kankaanranta, Hannu ;
Ainola, Mari ;
Saarto, Tiina ;
Myllarniemi, Marjukka .
ERJ OPEN RESEARCH, 2020, 6 (04) :1-9
[49]   Validation of the King's Brief Interstitial Lung Disease questionnaire in Idiopathic Pulmonary Fibrosis [J].
Prior, Thomas Skovhus ;
Hilberg, Ole ;
Shaker, Saher Burhan ;
Davidsen, Jesper Romhild ;
Hoyer, Nils ;
Birring, Surinder S. ;
Bendstrup, Elisabeth .
BMC PULMONARY MEDICINE, 2019, 19 (01)
[50]   Translation to Spanish and Validation of the Specific Saint George's Questionnaire for Idiopathic Pulmonary Fibrosis [J].
Capparelli, Ignacio ;
Fernandez, Martin ;
Saadia Otero, Marcela ;
Steimberg, Jimena ;
Brassesco, Maria ;
Campobasso, Ana ;
Palacios, Sandra ;
Caro, Fabian ;
Laura Alberti, Maria ;
Rabinovich, Roberto A. ;
Paulin, Francisco .
ARCHIVOS DE BRONCONEUMOLOGIA, 2018, 54 (02) :68-73