Efficient sampling of early signal arrival for estimation of perfusion and transit time in whole-brain arterial spin labeling

Magn Reson Med. 2012 Jul;68(1):179-87. doi: 10.1002/mrm.23222. Epub 2011 Dec 21.

Abstract

Arterial spin labeling can be used to measure both cerebral perfusion and arterial transit time. However, accurate estimation of these parameters requires adequate temporal sampling of the arterial spin labeling difference signal. In whole-brain multislice acquisitions, two factors reduce the accuracy of the parameter estimates: saturation of labeled blood in transit and inadequate sampling of early difference signal in superior slices. Label saturation arises when slices are acquired inferior-to-superior such that slice selection in proximal slices spoils the label for a distal slice. Inadequate sampling arises when the time spent acquiring inferior slices is too long to allow early sampling of the difference signal in superior slices. A novel approach to multislice imaging is proposed to address these two issues. In round-robin arterial spin labeling, slices are acquired in a different order after every pair of control-label acquisitions. Round-robin arterial spin labeling enables the acquisitions of all slices across the same range of postlabel delays in a descending superior-to-inferior order. This eliminates the temporal sampling problem and greatly reduces label saturation. Arterial transit time estimates obtained for the whole brain with round-robin arterial spin labeling show better agreement with a single-slice acquisition than do conventional multislice acquisitions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms*
  • Blood Flow Velocity / physiology
  • Brain / anatomy & histology
  • Brain / physiology*
  • Cerebral Arteries / anatomy & histology
  • Cerebral Arteries / physiology*
  • Cerebrovascular Circulation / physiology*
  • Humans
  • Image Enhancement / methods
  • Image Interpretation, Computer-Assisted / methods*
  • Magnetic Resonance Angiography / methods*
  • Pulsatile Flow / physiology
  • Reproducibility of Results
  • Sample Size
  • Sensitivity and Specificity
  • Spin Labels

Substances

  • Spin Labels