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An assessment of PET and CMR radiomic features for the detection of cardiac sarcoidosis

Authors :
Nouf A. Mushari
Georgios Soultanidis
Lisa Duff
Maria G. Trivieri
Zahi A. Fayad
Philip Robson
Charalampos Tsoumpas
Source :
Frontiers in Nuclear Medicine, Vol 4 (2024)
Publication Year :
2024
Publisher :
Frontiers Media S.A., 2024.

Abstract

BackgroundVisual interpretation of PET and CMR may fail to identify cardiac sarcoidosis (CS) with high specificity. This study aimed to evaluate the role of [18F]FDG PET and late gadolinium enhancement (LGE)-CMR radiomic features in differentiating CS from another cause of myocardial inflammation, in this case patients with cardiac-related clinical symptoms following COVID-19.Methods[18F]FDG PET and LGE-CMR were treated separately in this work. There were 35 post-COVID-19 (PC) and 40 CS datasets. Regions of interest were delineated manually around the entire left ventricle for the PET and LGE-CMR datasets. Radiomic features were then extracted. The ability of individual features to correctly identify image data as CS or PC was tested to predict the clinical classification of CS vs. PC using Mann–Whitney U-tests and logistic regression. Features were retained if the P-value was 0.5, and the accuracy was >0.7. After applying the correlation test, uncorrelated features were used as a signature (joint features) to train machine learning classifiers. For LGE-CMR analysis, to further improve the results, different classifiers were used for individual features besides logistic regression, and the results of individual features of each classifier were screened to create a signature that included all features that followed the previously mentioned criteria and used it them as input for machine learning classifiers.ResultsThe Mann–Whitney U-tests and logistic regression were trained on individual features to build a collection of features. For [18F]FDG PET analysis, the maximum target-to-background ratio (TBRmax) showed a high area under the curve (AUC) and accuracy with small P-values (

Details

Language :
English
ISSN :
26738880
Volume :
4
Database :
Directory of Open Access Journals
Journal :
Frontiers in Nuclear Medicine
Publication Type :
Academic Journal
Accession number :
edsdoj.53a2c58f0334ac8bdf5a9710274c1aa
Document Type :
article
Full Text :
https://doi.org/10.3389/fnume.2024.1324698