Single acquisition quantitative single-point electron paramagnetic resonance imaging

Magn Reson Med. 2013 Oct;70(4):1173-81. doi: 10.1002/mrm.24886. Epub 2013 Aug 1.

Abstract

Purpose: Electron paramagnetic resonance imaging has emerged as a promising noninvasive technology to dynamically image tissue oxygenation. Owing to its extremely short spin-spin relaxation times, electron paramagnetic resonance imaging benefits from a single-point imaging scheme where the entire free induction decay signal is captured using pure phase encoding. However, direct T2 (*)/pO2 quantification is inhibited owing to constant magnitude gradients which result in time-decreasing field of view. Therefore, conventional acquisition techniques require repeated imaging experiments with differing gradient amplitudes (typically 3), which results in long acquisition time.

Methods: In this study, gridding was evaluated as a method to reconstruct images with equal field of view to enable direct T2 (*)/pO2 quantification within a single imaging experiment. Additionally, an enhanced reconstruction technique that shares high spatial k-space regions throughout different phase-encoding time delays was investigated (k-space extrapolation).

Results: The combined application of gridding and k-space extrapolation enables pixelwise quantification of T2 (*) from a single acquisition with improved image quality across a wide range of phase-encoding time delays. The calculated T2 (*)/pO2 does not vary across this time range.

Conclusions: By utilizing gridding and k-space extrapolation, accurate T2 (*)/pO2 quantification can be achieved within a single data set to allow enhanced temporal resolution (by a factor of 3).

Keywords: EPR imaging; gridding; hypoxia; quantitative imaging; single point imaging; tissue oxygenation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Algorithms
  • Artifacts*
  • Electron Spin Resonance Spectroscopy / methods*
  • Image Enhancement / methods
  • Image Interpretation, Computer-Assisted / methods*
  • Magnetic Resonance Imaging / instrumentation
  • Magnetic Resonance Imaging / methods*
  • Molecular Imaging / instrumentation
  • Molecular Imaging / methods*
  • Oximetry / methods*
  • Oxygen / analysis*
  • Phantoms, Imaging
  • Reproducibility of Results
  • Sensitivity and Specificity

Substances

  • Oxygen