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Related Experiment Video

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Magnetic Resonance Imaging Quantification of Pulmonary Perfusion using Calibrated Arterial Spin Labeling
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Accelerated 3D-GRASE imaging improves quantitative multiple post labeling delay arterial spin labeling.

Markus Boland1, Rüdiger Stirnberg1, Eberhard D Pracht1

  • 1German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.

Magnetic Resonance in Medicine
|May 18, 2018
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Summary
This summary is machine-generated.

Accelerated 3D-GRASE with pseudo-continuous arterial spin labeling (PCASL) improves perfusion-weighted SNR and reduces quantification uncertainty. This makes advanced ASL methods clinically feasible within shorter scan times.

Keywords:
3D-GRASEcerebral blood flowmultiple post labeling delayperfusionpseudo-continuous arterial spin labelingsingle-shot

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Area of Science:

  • Magnetic Resonance Imaging
  • Neuroimaging
  • Medical Physics

Background:

  • Quantitative arterial spin labeling (ASL) provides non-invasive measurement of cerebral blood flow.
  • Accelerated imaging techniques are crucial for reducing scan times in ASL.
  • 3D-GRASE sequences offer fast volumetric coverage but can be limited by acceleration artifacts.

Purpose of the Study:

  • To evaluate the impact of accelerated single-shot 3D-GRASE acquisition on quantitative ASL.
  • To assess the effects on perfusion-weighted signal-to-noise ratio per unit scan time (TSNRPW) and quantification accuracy.
  • To compare single and multiple post-labeling delay (PLD) acquisitions under accelerated conditions.

Main Methods:

  • Five subjects underwent 3T MRI using pseudo-continuous ASL (PCASL) with accelerated 3D-GRASE.
  • Simulated and implemented 3-inversion pulse background suppression.
  • Compared TSNRPW for single PLD using segmented, GRAPPA, and CAIPIRINHA sampling.
  • Evaluated multiple PLD acquisitions (no acceleration, CAIPIRINHA, CAIPIRINHA with doubled PLDs) for cerebral blood flow and arterial transit time fit uncertainties.

Main Results:

  • CAIPIRINHA sampling increased TSNRPW by 11% compared to GRAPPA for single PLD.
  • Non-accelerated scans showed 35% higher TSNRPW than GRAPPA.
  • CAIPIRINHA sampling with multiple PLDs (6/12) reduced CBF fit uncertainty by 14%/16% (gray matter) and 34%/36% (white matter) compared to non-accelerated scans.

Conclusions:

  • Accelerated single-shot 3D-GRASE with PCASL achieves lower quantification uncertainties than time-matched segmented ASL.
  • This accelerated approach enables state-of-the-art ASL methods within clinically feasible scan times.
  • Acceptable image quality with minimal blurring and motion artifacts is achievable.