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Registered Bioimaging of Nanomaterials for Diagnostic and Therapeutic Monitoring
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Single-shot diffusion trace spectroscopic imaging using radial echo planar trajectories.

Andres Saucedo1,2, M Albert Thomas1,2,3

  • 1Radiological Sciences, University of California at Los Angeles, Los Angeles, California, USA.

Magnetic Resonance in Medicine
|May 10, 2024
PubMed
Summary
This summary is machine-generated.

This study demonstrates a new, faster method for measuring trace apparent diffusion coefficients (ADCs) using single-shot diffusion trace-weighted radial echo planar spectroscopic imaging (Trace DW-REPSI). The technique shows feasibility for phantom and in vivo imaging, offering quicker scans than traditional methods.

Keywords:
b‐valuediffusion‐weightingk‐spacepoint‐resolved spectroscopyradial echo planar spectroscopic imagingtrace apparent diffusion coefficient

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Area of Science:

  • Magnetic Resonance Imaging
  • Diffusion Tensor Imaging
  • Spectroscopic Imaging

Background:

  • Diffusion-weighted imaging (DWI) is crucial for characterizing tissue microstructure.
  • Accurate quantification of apparent diffusion coefficient (ADC) is vital for various neurological applications.
  • Conventional DWI methods can be time-consuming, limiting clinical utility.

Purpose of the Study:

  • To demonstrate the feasibility of single-shot diffusion trace-weighted radial echo planar spectroscopic imaging (Trace DW-REPSI).
  • To evaluate the performance of Trace DW-REPSI for quantifying trace ADC in phantoms and in vivo.
  • To assess the potential for faster ADC quantification using this novel sequence.

Main Methods:

  • Trace DW-REPSI datasets were acquired using a 3T scanner in phantoms and 10 healthy volunteers.
  • Maximum b-value of 1601 s/mm² and diffusion time of 10.75 ms were employed.
  • Radial acquisition self-navigation was utilized for phase and frequency correction.

Main Results:

  • Phantom trace ADCs showed excellent agreement with reported values.
  • In vivo ADCs correlated well with expected gray and white matter differences.
  • Extrapolated trace ADCs for tNAA, tCr, and tCho in gray/white matter ranged from 0.18-0.27 and 0.26-0.38 μm²/ms, respectively.
  • Overestimation of trace ADCs was attributed to the short diffusion time.

Conclusions:

  • This study presents the first demonstration of the single-shot Trace DW-REPSI sequence.
  • The Trace DW-REPSI sequence offers a significant reduction in scan time compared to conventional methods.
  • This technique holds promise for efficient and accurate trace ADC estimation in clinical settings.