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Related Experiment Video

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Diffusion Tensor Magnetic Resonance Imaging in Chronic Spinal Cord Compression
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Robust diffusion tensor imaging by spatiotemporal encoding: Principles and in vivo demonstrations.

Eddy Solomon1, Gilad Liberman1, Noam Nissan1,2

  • 1Department of Chemical Physics, Weizmann Institute of Science, Rehovot, Israel.

Magnetic Resonance in Medicine
|March 13, 2016
PubMed
Summary

Spatiotemporally encoded (SPEN) diffusion tensor imaging (DTI) offers improved robustness against field instabilities and distortions compared to single-shot methods. This makes SPEN DTI valuable for preclinical and clinical imaging, even in challenging environments.

Keywords:
b-value calculationsbrain DTIbreast DTIdiffusion-tensor imaging - DTIspatiotemporal encoding - SPEN

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Area of Science:

  • Magnetic Resonance Imaging
  • Biomedical Engineering
  • Neuroimaging

Background:

  • Diffusion Tensor Imaging (DTI) is crucial for visualizing white matter tracts.
  • Conventional single-shot DTI methods are susceptible to artifacts from magnetic field inhomogeneities and eddy currents.
  • Developing robust DTI techniques is essential for accurate preclinical and clinical applications.

Purpose of the Study:

  • To evaluate the utility of single-shot and interleaved spatiotemporally encoded (SPEN) methods for Diffusion Tensor Imaging (DTI).
  • To assess SPEN DTI performance across diverse preclinical and clinical settings.
  • To compare SPEN DTI against conventional single-shot DTI.

Main Methods:

  • A novel formalism was developed to analyze SPEN DTI data, accounting for spatially dependent b-matrix weightings from swept pulses and gradients.
  • SPEN DTI performance was rigorously tested using phantoms, ex vivo samples, and in vivo scans of mouse brains and human lactating breasts.
  • Referenceless methods were explored for interleaved SPEN data acquisition to enhance resolution.

Main Results:

  • SPEN DTI data demonstrated reduced sensitivity to B0 field inhomogeneities and eddy current-induced distortions compared to single-shot DTI, in both ex vivo and in vivo studies.
  • Interleaved SPEN acquisitions, particularly with referenceless methods, offered further improvements in image resolution.
  • Successful DTI measurements were obtained in challenging imaging scenarios.

Conclusions:

  • SPEN-based DTI sequences exhibit significant robustness against magnetic field instabilities and heterogeneities.
  • These SPEN sequences facilitate DTI experiments with high sensitivity and resolution, even in demanding preclinical and clinical environments.
  • SPEN DTI represents a promising advancement for neuroimaging and other biomedical applications requiring robust diffusion measurements.