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Time efficient whole-brain coverage with MR Fingerprinting using slice-interleaved echo-planar-imaging

Magnetic resonance fingerprinting (MRF) is a promising method for fast simultaneous quantification of multiple tissue parameters. The objective of this study is to improve the coverage of MRF based on echo-planar imaging (MRF-EPI) by using a slice-interleaved acquisition scheme. For this, the MRF-EP...

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Detalles Bibliográficos
Autores principales: Rieger, Benedikt, Akçakaya, Mehmet, Pariente, José C., Llufriu, Sara, Martinez-Heras, Eloy, Weingärtner, Sebastian, Schad, Lothar R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923901/
https://www.ncbi.nlm.nih.gov/pubmed/29703978
http://dx.doi.org/10.1038/s41598-018-24920-z
Descripción
Sumario:Magnetic resonance fingerprinting (MRF) is a promising method for fast simultaneous quantification of multiple tissue parameters. The objective of this study is to improve the coverage of MRF based on echo-planar imaging (MRF-EPI) by using a slice-interleaved acquisition scheme. For this, the MRF-EPI is modified to acquire several slices in a randomized interleaved manner, increasing the effective repetition time of the spoiled gradient echo readout acquisition in each slice. Per-slice matching of the signal-trace to a precomputed dictionary allows the generation of T(1) and T(2)* maps with integrated B(1)(+) correction. Subsequent compensation for the coil sensitivity profile and normalization to the cerebrospinal fluid additionally allows for quantitative proton density (PD) mapping. Numerical simulations are performed to optimize the number of interleaved slices. Quantification accuracy is validated in phantom scans and feasibility is demonstrated in-vivo. Numerical simulations suggest the acquisition of four slices as a trade-off between quantification precision and scan-time. Phantom results indicate good agreement with reference measurements (Difference T(1): −2.4 ± 1.1%, T(2)*: −0.5 ± 2.5%, PD: −0.5 ± 7.2%). In-vivo whole-brain coverage of T(1), T(2)* and PD with 32 slices was acquired within 3:36 minutes, resulting in parameter maps of high visual quality and comparable performance with single-slice MRF-EPI at 4-fold scan-time reduction.