Attenuation correction using 3D deep convolutional neural network for brain 18F-FDG PET/MR: Comparison with Atlas, ZTE and CT based attenuation correction.
Journal
PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081
Informations de publication
Date de publication:
2019
2019
Historique:
received:
24
06
2019
accepted:
13
09
2019
entrez:
8
10
2019
pubmed:
8
10
2019
medline:
14
3
2020
Statut:
epublish
Résumé
One of the main technical challenges of PET/MRI is to achieve an accurate PET attenuation correction (AC) estimation. In current systems, AC is accomplished by generating an MRI-based surrogate computed tomography (CT) from which AC-maps are derived. Nevertheless, all techniques currently implemented in clinical routine suffer from bias. We present here a convolutional neural network (CNN) that generated AC-maps from Zero Echo Time (ZTE) MR images. Seventy patients referred to our institution for 18FDG-PET/MR exam (SIGNA PET/MR, GE Healthcare) as part of the investigation of suspected dementia, were included. 23 patients were added to the training set of the manufacturer and 47 were used for validation. Brain computed tomography (CT) scan, two-point LAVA-flex MRI (for atlas-based AC) and ZTE-MRI were available in all patients. Three AC methods were evaluated and compared to CT-based AC (CTAC): one based on a single head-atlas, one based on ZTE-segmentation and one CNN with a 3D U-net architecture to generate AC maps from ZTE MR images. Impact on brain metabolism was evaluated combining voxel and regions-of-interest based analyses with CTAC set as reference. The U-net AC method yielded the lowest bias, the lowest inter-individual and inter-regional variability compared to PET images reconstructed with ZTE and Atlas methods. The impact on brain metabolism was negligible with average errors of -0.2% in most cortical regions. These results suggest that the U-net AC is more reliable for correcting photon attenuation in brain FDG-PET/MR than atlas-AC and ZTE-AC methods.
Identifiants
pubmed: 31589623
doi: 10.1371/journal.pone.0223141
pii: PONE-D-19-16876
pmc: PMC6779234
doi:
Substances chimiques
Fluorodeoxyglucose F18
0Z5B2CJX4D
Types de publication
Comparative Study
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0223141Subventions
Organisme : NIDDK NIH HHS
ID : P30 DK040561
Pays : United States
Organisme : NIBIB NIH HHS
ID : P41 EB022544
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA165221
Pays : United States
Déclaration de conflit d'intérêts
MK received a research grant from GE Healthcare. SK and FW are GE Healthcare employees. Only non-GE employees had control of inclusion of data and information that might present a conflict of interest for authors who are employees of GE Healthcare. No other potential conflict of interest relevant to this article was reported. AK received honoraria for lectures from GE Healthcare and Piramal. MOH received honoraria for lectures from Lilly. This does not alter our adherence to PLOS ONE policies on sharing data and materials. The other authors do not present any conflict of interest.
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