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Subject-specific timing adaption in time-encoded arterial spin labeling imaging.

Nora-Josefin Breutigam1, Daniel Christopher Hoinkiss2, Simon Konstandin2,3

  • 1Imaging Physics, Fraunhofer Institute for Digital Medicine MEVIS, Max-von-Laue-Str. 2, 28359, Bremen, Germany. nora-josefin.breutigam@mevis.fraunhofer.de.

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Summary

An adaptive algorithm optimizes arterial spin labeling (ASL) timing, reducing artifacts in cerebral blood flow (CBF) and arterial transit time (ATT) quantification for improved MRI accuracy.

Keywords:
Arterial spin labelingArterial transit delay artifactsFree-lunch approachSubject-specific timingTime-encoded pCASL

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Area of Science:

  • Magnetic Resonance Imaging
  • Neuroimaging Techniques

Background:

  • Arterial spin labeling (ASL) is challenged by arterial transit time (ATT) variability, leading to arterial transit delay (ATD) artifacts.
  • Suboptimal post-labeling delay (PLD) and bolus durations hinder accurate cerebral blood flow (CBF) and ATT quantification, particularly in pathological conditions and with Hadamard-encoded pseudocontinuous ASL (H-pCASL).

Purpose of the Study:

  • To develop and evaluate an adaptive algorithm for optimizing pCASL sub-bolus timing.
  • To assess the impact of individually adjusted timing on CBF and ATT quantification accuracy and variability.

Main Methods:

  • Utilized an adaptive Walsh-ordered pCASL sequence with an automatic feedback algorithm to individually adjust pCASL sub-bolus timing in five healthy volunteers.
  • Compared quantification results (CBF, ATT, standard deviations) with recommended and suboptimal timings using 3 T MRI.

Main Results:

  • The algorithm successfully adjusted pCASL sub-bolus PLD individually within recommended ranges for healthy subjects.
  • Demonstrated mean intra-subject adjustment deviations of 47.15 ms (single-shot) and 44.5 ms (segmented acquisition) across three repetitions.

Conclusions:

  • Initial assessment in healthy volunteers shows promise for the adaptive timing algorithm.
  • Further studies are required to validate transferability to patient populations and assess clinical benefits.