Reproducibility of Segmentation-based Myocardial Radiomic Features with Cardiac MRI.
Journal
Radiology. Cardiothoracic imaging
ISSN: 2638-6135
Titre abrégé: Radiol Cardiothorac Imaging
Pays: United States
ID NLM: 101748663
Informations de publication
Date de publication:
25 Jun 2020
25 Jun 2020
Historique:
received:
10
10
2019
revised:
19
02
2020
accepted:
04
03
2020
entrez:
1
8
2020
pubmed:
1
8
2020
medline:
1
8
2020
Statut:
epublish
Résumé
To investigate reproducibility of myocardial radiomic features with cardiac MRI. Test-retest studies were performed with a 3-T MRI system using commonly used cardiac MRI sequences of cine balanced steady-state free precession (cine bSSFP), T1-weighted and T2-weighted imaging, and quantitative T1 and T2 mapping in phantom experiments and 10 healthy participants (mean ± standard deviation age, 29 years ± 13). In addition, this study assessed repeatability in 51 patients (56 years ± 14) who underwent imaging twice during the same session. Three readers independently delineated the myocardium to investigate inter- and intraobserver reproducibility of radiomic features. A total of 1023 radiomic features were extracted by using PyRadiomics ( Different reproducibility patterns were observed among sequences in in vivo test-retest studies. In cine bSSFP, the gray-level run-length matrix was the most reproducible feature family, and the wavelet low-pass filter applied horizontally and vertically was the most reproducible image filter. In T1 and T2 maps, intensity-based statistics (first-order) and gray-level co-occurrence matrix features were the most reproducible feature families, without a dominant reproducible image filter. Across all sequences, gray-level nonuniformity was the most frequently identified reproducible feature name. In inter- and intraobserver reproducibility studies, respectively, only 32%-47% and 61%-73% of features were identified as reproducible. Only a small subset of myocardial radiomic features was reproducible, and these reproducible radiomic features varied among different sequences.
Identifiants
pubmed: 32734275
doi: 10.1148/ryct.2020190216
pmc: PMC7377242
doi:
Types de publication
Journal Article
Langues
eng
Pagination
e190216Subventions
Organisme : NHLBI NIH HHS
ID : R01 HL127015
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL129157
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL129185
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL154744
Pays : United States
Commentaires et corrections
Type : CommentIn
Informations de copyright
2020 by the Radiological Society of North America, Inc.
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