Simultaneous Multislice Accelerated TSE for Improved Spatiotemporal Resolution and Diagnostic Accuracy in Magnetic Resonance Neurography: A Feasibility Study.


Journal

Investigative radiology
ISSN: 1536-0210
Titre abrégé: Invest Radiol
Pays: United States
ID NLM: 0045377

Informations de publication

Date de publication:
01 05 2023
Historique:
medline: 18 4 2023
pubmed: 3 2 2023
entrez: 2 2 2023
Statut: ppublish

Résumé

This study aims to evaluate the utility of simultaneous multislice (SMS) acceleration for routine magnetic resonance neurography (MRN) at 3 T. Patients with multiple sclerosis underwent MRN of the sciatic nerve consisting of a standard fat-saturated T2-weighted turbo spin echo (TSE) sequence using integrated parallel acquisition technique (PAT2) acceleration and 2 T2 TSE sequences using a combination of PAT-SMS acceleration (1) to reduce scan time (PAT2-SMS2; SMS-TSE FAST ) and (2) for time neutral increase of in-plane resolution (PAT1-SMS2; SMS-TSE HR ). Acquisition times were 5:29 minutes for the standard T2 TSE, 3:12 minutes for the SMS-TSE FAST , and 5:24 minutes for the SMS-TSE HR . Six qualitative imaging parameters were analyzed by 2 blinded readers using a 5-point Likert scale and T2 nerve lesions were quantified, respectively. Qualitative and quantitative image parameters were compared, and both interrater and intrarater reproducibility were statistically assessed. In addition, signal-to-noise ratio/contrast-to-noise ratio (CNR) was obtained in healthy controls using the exact same imaging protocol. A total of 15 patients with MS (mean age ± standard deviation, 38.1 ± 11 years) and 10 healthy controls (mean age, 29.1 ± 7 years) were enrolled in this study. CNR analysis was highly reliable (intraclass correlation coefficient, 0.755-0.948) and revealed a significant CNR decrease for the sciatic nerve for both SMS protocols compared with standard T2 TSE (SMS-TSE FAST /SMS-TSE HR , -39%/-55%; P ≤ 0.01). Intrarater and interrater reliability of qualitative image review was good to excellent (κ: 0.672-0.971/0.617-0.883). Compared with the standard T2 TSE sequence, both SMS methods were shown to be superior in reducing pulsatile flow artifacts ( P < 0.01). Ratings for muscle border sharpness, detailed muscle structures, nerve border sharpness, and nerve fascicular structure did not differ significantly between the standard T2 TSE and the SMS-TSE FAST ( P > 0.05) and were significantly better for the SMS-TSE HR than for standard T2 TSE ( P < 0.001). Muscle signal homogeneity was mildly inferior for both SMS-TSE FAST ( P > 0.05) and SMS-TSE HR ( P < 0.001). A significantly higher number of T2 nerve lesions were detected by SMS-TSE HR ( P ≤ 0.01) compared with the standard T2 TSE and SMS-TSE FAST , whereas no significant difference was observed between the standard T2 TSE and SMS-TSE FAST . Implementation of SMS offers either to substantially reduce acquisition time by over 40% without significantly impeding image quality compared with the standard T2 TSE or to increase in-plane resolution for a high-resolution approach and improved depiction of T2 nerve lesions while keeping acquisition times constant. This addresses the specific needs of MRN by providing different imaging approaches for 2D clinical MRN.

Identifiants

pubmed: 36729753
doi: 10.1097/RLI.0000000000000940
pii: 00004424-202305000-00008
doi:

Types de publication

Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

363-371

Informations de copyright

Copyright © 2022 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest and sources of funding: F.P. was supported by a Physician-Scientist Fellowship of the Medical Faculty of the University of Heidelberg. S.H. (SFB 1118), D.S. (SFB 1118), and M.B. (SFB 1158) were supported by the German Research Foundation. F.C. is an employee of Siemens Healthcare GmbH and was involved in the technical development of the TSE SMS sequence prototype. T.H. is supported in part by the Dietmar Hopp Foundation (project no. 1DH2011152). For the remaining authors, none were declared.

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Auteurs

Fabian Preisner (F)

From the Department of Neuroradiology, Heidelberg University Hospital, Heidelberg.

Jennifer C Hayes (JC)

From the Department of Neuroradiology, Heidelberg University Hospital, Heidelberg.

Tobias Charlet (T)

From the Department of Neuroradiology, Heidelberg University Hospital, Heidelberg.

Flavio Carinci (F)

Magnetic Resonance, Siemens Healthcare GmbH, Erlangen.

Thomas Hielscher (T)

Division of Biostatistics, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Daniel Schwarz (D)

From the Department of Neuroradiology, Heidelberg University Hospital, Heidelberg.

Dominik F Vollherbst (DF)

From the Department of Neuroradiology, Heidelberg University Hospital, Heidelberg.

Michael O Breckwoldt (MO)

From the Department of Neuroradiology, Heidelberg University Hospital, Heidelberg.

Jessica Jesser (J)

From the Department of Neuroradiology, Heidelberg University Hospital, Heidelberg.

Sabine Heiland (S)

From the Department of Neuroradiology, Heidelberg University Hospital, Heidelberg.

Martin Bendszus (M)

From the Department of Neuroradiology, Heidelberg University Hospital, Heidelberg.

Tim Hilgenfeld (T)

From the Department of Neuroradiology, Heidelberg University Hospital, Heidelberg.

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