Validation of a Denoising Method Using Deep Learning-Based Reconstruction to Quantify Multiple Sclerosis Lesion Load on Fast FLAIR Imaging.


Journal

AJNR. American journal of neuroradiology
ISSN: 1936-959X
Titre abrégé: AJNR Am J Neuroradiol
Pays: United States
ID NLM: 8003708

Informations de publication

Date de publication:
08 2022
Historique:
received: 20 12 2021
accepted: 13 06 2022
pubmed: 29 7 2022
medline: 21 3 2023
entrez: 28 7 2022
Statut: ppublish

Résumé

Accurate quantification of WM lesion load is essential for the care of patients with multiple sclerosis. We tested whether the combination of accelerated 3D-FLAIR and denoising using deep learning-based reconstruction could provide a relevant strategy while shortening the imaging examination. Twenty-eight patients with multiple sclerosis were prospectively examined using 4 implementations of 3D-FLAIR with decreasing scan times (4 minutes 54 seconds, 2 minutes 35 seconds, 1 minute 40 seconds, and 1 minute 15 seconds). Each FLAIR sequence was reconstructed without and with denoising using deep learning-based reconstruction, resulting in 8 FLAIR sequences per patient. Image quality was assessed with the Likert scale, apparent SNR, and contrast-to-noise ratio. Manual and automatic lesion segmentations, performed randomly and blindly, were quantitatively evaluated against ground truth using the absolute volume difference, true-positive rate, positive predictive value, Dice similarity coefficient, Hausdorff distance, and F1 score based on the lesion count. The Wilcoxon signed-rank test and 2-way ANOVA were performed. Both image-quality evaluation and the various metrics showed deterioration when the FLAIR scan time was accelerated. However, denoising using deep learning-based reconstruction significantly improved subjective image quality and quantitative performance metrics, particularly for manual segmentation. Overall, denoising using deep learning-based reconstruction helped to recover contours closer to those from the criterion standard and to capture individual lesions otherwise overlooked. The Dice similarity coefficient was equivalent between the 2-minutes-35-seconds-long FLAIR with denoising using deep learning-based reconstruction and the 4-minutes-54-seconds-long reference FLAIR sequence. Denoising using deep learning-based reconstruction helps to recognize multiple sclerosis lesions buried in the noise of accelerated FLAIR acquisitions, a possibly useful strategy to efficiently shorten the scan time in clinical practice.

Sections du résumé

BACKGROUND AND PURPOSE
Accurate quantification of WM lesion load is essential for the care of patients with multiple sclerosis. We tested whether the combination of accelerated 3D-FLAIR and denoising using deep learning-based reconstruction could provide a relevant strategy while shortening the imaging examination.
MATERIALS AND METHODS
Twenty-eight patients with multiple sclerosis were prospectively examined using 4 implementations of 3D-FLAIR with decreasing scan times (4 minutes 54 seconds, 2 minutes 35 seconds, 1 minute 40 seconds, and 1 minute 15 seconds). Each FLAIR sequence was reconstructed without and with denoising using deep learning-based reconstruction, resulting in 8 FLAIR sequences per patient. Image quality was assessed with the Likert scale, apparent SNR, and contrast-to-noise ratio. Manual and automatic lesion segmentations, performed randomly and blindly, were quantitatively evaluated against ground truth using the absolute volume difference, true-positive rate, positive predictive value, Dice similarity coefficient, Hausdorff distance, and F1 score based on the lesion count. The Wilcoxon signed-rank test and 2-way ANOVA were performed.
RESULTS
Both image-quality evaluation and the various metrics showed deterioration when the FLAIR scan time was accelerated. However, denoising using deep learning-based reconstruction significantly improved subjective image quality and quantitative performance metrics, particularly for manual segmentation. Overall, denoising using deep learning-based reconstruction helped to recover contours closer to those from the criterion standard and to capture individual lesions otherwise overlooked. The Dice similarity coefficient was equivalent between the 2-minutes-35-seconds-long FLAIR with denoising using deep learning-based reconstruction and the 4-minutes-54-seconds-long reference FLAIR sequence.
CONCLUSIONS
Denoising using deep learning-based reconstruction helps to recognize multiple sclerosis lesions buried in the noise of accelerated FLAIR acquisitions, a possibly useful strategy to efficiently shorten the scan time in clinical practice.

Identifiants

pubmed: 35902124
pii: ajnr.A7589
doi: 10.3174/ajnr.A7589
pmc: PMC9575422
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1099-1106

Informations de copyright

© 2022 by American Journal of Neuroradiology.

Auteurs

T Yamamoto (T)

From the Institut de Bio-imagerie (T.Y., H.F., L.D., V.D., T.T.), University Bordeaux, Bordeaux, France.

C Lacheret (C)

Neuroimagerie Diagnostique et Thérapeutique (C.L., V.D., T.T.).

H Fukutomi (H)

From the Institut de Bio-imagerie (T.Y., H.F., L.D., V.D., T.T.), University Bordeaux, Bordeaux, France.

R A Kamraoui (RA)

Laboratoire Bordelais de Recherche en Informatique (R.A.K., P.C.), University Bordeaux, Le Centre National de la Recherche Scientifique, Bordeaux Institut National Polytechnique, Talence, France.

L Denat (L)

From the Institut de Bio-imagerie (T.Y., H.F., L.D., V.D., T.T.), University Bordeaux, Bordeaux, France.

B Zhang (B)

Canon Medical Systems Europe (B.Z.), Zoetermeer, the Netherlands.

V Prevost (V)

Canon Medical Systems (V.P., B.T.), Tochigi, Japan.

L Zhang (L)

Canon Medical Systems China (L.Z.), Beijing, China.

A Ruet (A)

Service de Neurologie (A.R.), Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.

B Triaire (B)

Canon Medical Systems (V.P., B.T.), Tochigi, Japan.

V Dousset (V)

From the Institut de Bio-imagerie (T.Y., H.F., L.D., V.D., T.T.), University Bordeaux, Bordeaux, France.
Neuroimagerie Diagnostique et Thérapeutique (C.L., V.D., T.T.).
NeurocentreMagendie (V.D., T.T.), University of Bordeaux, L'Institut National de la Santé et de la Recherche Médicale, Bordeaux, France.

P Coupé (P)

Laboratoire Bordelais de Recherche en Informatique (R.A.K., P.C.), University Bordeaux, Le Centre National de la Recherche Scientifique, Bordeaux Institut National Polytechnique, Talence, France.

T Tourdias (T)

From the Institut de Bio-imagerie (T.Y., H.F., L.D., V.D., T.T.), University Bordeaux, Bordeaux, France thomas.tourdias@chu-bordeaux.fr.
Neuroimagerie Diagnostique et Thérapeutique (C.L., V.D., T.T.).
NeurocentreMagendie (V.D., T.T.), University of Bordeaux, L'Institut National de la Santé et de la Recherche Médicale, Bordeaux, France.

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