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Accelerated high-bandwidth MR spectroscopic imaging using compressed sensing.
Cao, Peng; Shin, Peter J; Park, Ilwoo; Najac, Chloe; Marco-Rius, Irene; Vigneron, Daniel B; Nelson, Sarah J; Ronen, Sabrina M; Larson, Peder E Z.
Afiliação
  • Cao P; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA.
  • Shin PJ; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA.
  • Park I; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA.
  • Najac C; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA.
  • Marco-Rius I; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA.
  • Vigneron DB; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA.
  • Nelson SJ; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA.
  • Ronen SM; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA.
  • Larson PE; Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA.
Magn Reson Med ; 76(2): 369-79, 2016 08.
Article em En | MEDLINE | ID: mdl-27228088
ABSTRACT

PURPOSE:

To develop a compressed sensing (CS) acceleration method with a high spectral bandwidth exploiting the spatial-spectral sparsity of MR spectroscopic imaging (MRSI).

METHODS:

Accelerations were achieved using blip gradients during the readout to perform nonoverlapped and stochastically delayed random walks in kx -ky -t space, combined with block-Hankel matrix completion for efficient reconstruction. Both retrospective and prospective CS accelerations were applied to (13) C MRSI experiments, including in vivo rodent brain and liver studies with administrations of hyperpolarized [1-(13) C] pyruvate at 7.0 Tesla (T) and [2-(13) C] dihydroxyacetone at 3.0 T, respectively.

RESULTS:

In retrospective undersampling experiments using in vivo 7.0 T data, the proposed method preserved spectral, spatial, and dynamic fidelities with R(2) ≥ 0.96 and ≥ 0.87 for pyruvate and lactate signals, respectively, 750-Hz spectral separation, and up to 6.6-fold accelerations. In prospective in vivo experiments, with 3.8-fold acceleration, the proposed method exhibited excellent spatial localization of metabolites and peak recovery for pyruvate and lactate at 7.0 T as well as for dihydroxyacetone and its metabolic products with a 4.5-kHz spectral span (140 ppm at 3.0 T).

CONCLUSIONS:

This study demonstrated the feasibility of a new CS approach to accelerate high spectral bandwidth MRSI experiments. Magn Reson Med 76369-379, 2016. © 2016 Wiley Periodicals, Inc.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Algoritmos / Química Encefálica / Imageamento por Ressonância Magnética / Compressão de Dados / Imagem Molecular / Espectroscopia de Ressonância Magnética Nuclear de Carbono-13 / Fígado Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Algoritmos / Química Encefálica / Imageamento por Ressonância Magnética / Compressão de Dados / Imagem Molecular / Espectroscopia de Ressonância Magnética Nuclear de Carbono-13 / Fígado Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article