4.5 Review

Edited 1H Magnetic Resonance Spectroscopy In Vivo: Methods and Metabolites

Journal

MAGNETIC RESONANCE IN MEDICINE
Volume 77, Issue 4, Pages 1377-1389

Publisher

WILEY
DOI: 10.1002/mrm.26619

Keywords

J-coupling; echo-time averaging; J-difference editing; constant-time PRESS; quantum filtering; metabolites; magnetic resonance spectroscopy (MRS)

Funding

  1. Alberta Children's Hospital Research Institute, University of Calgary
  2. Hotchkiss Brain Institute, University of Calgary
  3. NIH [R01 EB016089, P41 EB015909]

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The Proton magnetic resonance (H-1-MRS) spectrum contains information about the concentration of tissue metabolites within a predefined region of interest (a voxel). The conventional spectrum in some cases obscures information about less abundant metabolites due to limited separation and complex splitting of the metabolite peaks. One method to detect these metabolites is to reduce the complexity of the spectrum using editing. This review provides an overview of the one-dimensional editing methods available to interrogate these obscured metabolite peaks. These methods include sequence optimizations, echo-time averaging, J-difference editing methods (single BASING, dual BASING, and MEGAPRESS), constant-time PRESS, and multiple quantum filtering. It then provides an overview of the brain metabolites whose detection can benefit from one or more of these editing approaches, including ascorbic acid, gamma-aminobutyric acid, lactate, aspartate, N-acetyl aspartyl glutamate, 2-hydroxyglutarate, glutathione, glutamate, glycine, and serine. (C) 2017 International Society for Magnetic Resonance in Medicine.

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