Publication: Evaluation of ultrafastwave-controlled aliasing in parallel imaging 3d-flair in the visualization and volumetric estimation of cerebralwhite matter lesions
Issued Date
2021-09-01
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ISSN
1936959X
01956108
01956108
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2-s2.0-85114868507
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Mahidol University
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SCOPUS
Bibliographic Citation
American Journal of Neuroradiology. Vol.42, No.9 (2021), 1584-1590
Suggested Citation
C. Ngamsombat, A. L.M. Gonçalves Filho, M. G.F. Longo, S. F. Cauley, K. Setsompop, J. E. Kirsch, Q. Tian, Q. Fan, D. Polak, W. Liu, W. C. Lo, R. Gilberto González, P. W. Schaefer, O. Rapalino, J. Conklin, S. Y. Huang Evaluation of ultrafastwave-controlled aliasing in parallel imaging 3d-flair in the visualization and volumetric estimation of cerebralwhite matter lesions. American Journal of Neuroradiology. Vol.42, No.9 (2021), 1584-1590. doi:10.3174/ajnr.A7191 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/77889
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Title
Evaluation of ultrafastwave-controlled aliasing in parallel imaging 3d-flair in the visualization and volumetric estimation of cerebralwhite matter lesions
Abstract
BACKGROUND AND PURPOSE: Our aim was to evaluate an ultrafast 3D-FLAIR sequence using Wave-controlled aliasing in parallel imaging encoding (Wave-FLAIR) compared with standard 3D-FLAIR in the visualization and volumetric estimation of cerebral white matter lesions in a clinical setting. MATERIALS AND METHODS: Forty-two consecutive patients underwent 3T brain MR imaging, including standard 3D-FLAIR (acceleration factor=2, scan time = 7 minutes 50 seconds) and resolution-matched ultrafast Wave-FLAIR sequences (acceleration factor =6, scan time=2 minutes 45 seconds for the 20-channel coil; acceleration factor=9, scan time =1 minute 50 seconds for the 32-channel coil) as part of clinical evaluation for demyelinating disease. Automated segmentation of cerebral white matter lesions was performed using the Lesion Segmentation Tool in SPM. Student t tests, intraclass correlation coefficients, relative lesion volume difference, and Dice similarity coefficients were used to compare volumetric measurements among sequences. Two blinded neuroradiologists evaluated the visualization of white matter lesions, artifacts, and overall diagnostic quality using a predefined 5- point scale. RESULTS: Standard and Wave-FLAIR sequences showed excellent agreement of lesion volumes with an intraclass correlation coefficient of 0.99 and mean Dice similarity coefficient of 0.97 (SD, 0.05) (range, 0.84-0.99). Wave-FLAIR was noninferior to standard FLAIR for visualization of lesions and motion. The diagnostic quality for Wave-FLAIR was slightly greater than for standard FLAIR for infratentorial lesions (P<.001), and there were fewer pulsation artifacts on Wave-FLAIR compared with standard FLAIR (P<.001). CONCLUSIONS: Ultrafast Wave-FLAIR provides superior visualization of infratentorial lesions while preserving overall diagnostic quality and yields white matter lesion volumes comparable with those estimated using standard FLAIR. The availability of ultrafast Wave-FLAIR may facilitate the greater use of 3D-FLAIR sequences in the evaluation of patients with suspected demyelinating disease.