Accelerating TOF-MRA: The impact of the combined use of compressed sensitivity encoding and spiral imaging.

Acceleration Feasibility studies Magnetic resonance angiography Signal-to-noise ratio Volunteers

Journal

Magnetic resonance imaging
ISSN: 1873-5894
Titre abrégé: Magn Reson Imaging
Pays: Netherlands
ID NLM: 8214883

Informations de publication

Date de publication:
11 2023
Historique:
received: 19 10 2022
revised: 29 06 2023
accepted: 29 06 2023
medline: 14 9 2023
pubmed: 6 7 2023
entrez: 5 7 2023
Statut: ppublish

Résumé

To evaluate the image quality of the combined technique of compressed sensitivity encoding (CS) and spiral imaging in time-of-flight magnetic resonance angiography (TOF-MRA), which is approximately 2.5 times faster than conventional methods. Twenty volunteers underwent four TOF-MRA sequences: sensitivity encoding (SENSE) with acceleration factor of 4 (acquisition time: 4:55 min), CS with acceleration factor of 10.9, and spiral and CS-spiral (both 1:55 min). A quantitative image analysis (signal-to-noise ratio [SNR], contrast, and full width at half maximum [FWHM] edge criterion measurements) was performed on four TOF sequences. For qualitative image analysis, two board-certified radiologists evaluated the overall depiction of the proximal, intermediate, and distal branches in CS, spiral, and CS-spiral images using SENSE as a reference. The SNR of BA in spiral and CS-spiral imaging was significantly lower than that in SENSE (p = 0.009). The contrasts of ACA and BA in CS-spiral were significantly higher and those in spiral were significantly lower than those in SENSE (p < 0.001). The FWHM in the CS image was significantly higher than that of SENSE; however, no significant differences were observed between the spiral or CS-spiral and SENSE. In qualitative analysis, the depiction of proximal vascular branches was significantly impaired in spiral than in others and that of distal vascular branches was significantly impaired in CS than in others (p < 0.001). In TOF-MRA, which is approximately 2.5 times faster than conventional methods, the combined use of CS and spiral imaging demonstrated an improvement in image quality compared to either CS or spiral imaging alone. The image quality of Compressed SENSE and spiral imaging is particularly poor in the proximal and distal vascular branches, respectively at an extremely high acceleration factor; however, CS-spiral provided stable image quality in all regions as compared with the SENSE technique.

Identifiants

pubmed: 37406743
pii: S0730-725X(23)00116-9
doi: 10.1016/j.mri.2023.06.019
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

28-36

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest Takeshi Nakaura has received research support from Nemoto Kyorindo Co., Ltd. Toshinori Hirai has received research support from Canon Medical Systems. The department of diagnostic imaging analysis, to which Dr. Kidoh belongs, is an endowed chair supported by Philips Healthcare. Masami Yoneyama is an employee of Philips Healthcare, and he installed CS-Spiral to MRI as a research sequence. The Nemoto Kyorindo Co., Ltd., Philips Healthcare and Canon Medical Systems had no control over the interpretation or publication of this work. Takeshi Nakaura controlled the study data. We used a prototype sequence for this volunteer study. Masami Yoneyama is responsible for providing technical advice on parameter settings, and for creating the schema and description of CS-Spiral technique.

Auteurs

Kosuke Morita (K)

Department of Radiology, Kumamoto University Hospital, Honjo 1-1-1, Kumamoto, Japan.

Hiroyuki Uetani (H)

Department of Diagnostic Radiology, Graduate School of Medical Sciences, Kumamoto University, Honjo 1-1-1, Kumamoto, Japan.

Takeshi Nakaura (T)

Department of Diagnostic Radiology, Graduate School of Medical Sciences, Kumamoto University, Honjo 1-1-1, Kumamoto, Japan. Electronic address: kff00712@nifty.com.

Masami Yoneyama (M)

Philips Japan, 13-37, Kohnan 2-chome, Tokyo, Japan.

Yasunori Nagayama (Y)

Department of Diagnostic Radiology, Graduate School of Medical Sciences, Kumamoto University, Honjo 1-1-1, Kumamoto, Japan.

Masafumi Kidoh (M)

Department of Diagnostic Radiology, Graduate School of Medical Sciences, Kumamoto University, Honjo 1-1-1, Kumamoto, Japan.

Naoki Shinojima (N)

Department of Neurosurgery, Graduate School of Medical Sciences, Kumamoto University, Honjo 1-1-1, Kumamoto, Japan.

Tadashi Hamasaki (T)

Department of Neurosurgery, Graduate School of Medical Sciences, Kumamoto University, Honjo 1-1-1, Kumamoto, Japan.

Akitake Mukasa (A)

Department of Neurosurgery, Graduate School of Medical Sciences, Kumamoto University, Honjo 1-1-1, Kumamoto, Japan.

Toshinori Hirai (T)

Department of Diagnostic Radiology, Graduate School of Medical Sciences, Kumamoto University, Honjo 1-1-1, Kumamoto, Japan.

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