Clinical evaluation of an arterial-spin-labeling product sequence in steno-occlusive disease of the brain

PLoS One. 2014 Feb 6;9(2):e87143. doi: 10.1371/journal.pone.0087143. eCollection 2014.

Abstract

Introduction: In brain perfusion imaging, arterial spin labeling (ASL) is a noninvasive alternative to dynamic susceptibility contrast-magnetic resonance imaging (DSC-MRI). For clinical imaging, only product sequences can be used. We therefore analyzed the performance of a product sequence (PICORE-PASL) included in an MRI software-package compared with DSC-MRI in patients with steno-occlusion of the MCA or ICA >70%.

Methods: Images were acquired on a 3T MRI system and qualitatively analyzed by 3 raters. For a quantitative analysis, cortical ROIs were placed in co-registered ASL and DSC images. Pooled data for ASL-cerebral blood flow (CBF) and DSC-CBF were analyzed by Spearman's correlation and the Bland-Altman (BA)-plot.

Results: In 28 patients, 11 ASL studies were uninterpretable due to patient motion. Of the remaining patients, 71% showed signs of delayed tracer arrival. A weak correlation for DSC-relCBF vs ASL-relCBF (r = 0.24) and a large spread of values in the BA-plot owing to unreliable CBF-measurement was found.

Conclusion: The PICORE ASL product sequence is sensitive for estimation of delayed tracer arrival, but cannot be recommended to measure CBF in steno-occlusive disease. ASL-sequences that are less sensitive to patient motion and correcting for delayed blood flow should be available in the clinical setting.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Arterial Occlusive Diseases / diagnosis*
  • Arterial Occlusive Diseases / pathology*
  • Artifacts
  • Brain / blood supply*
  • Cerebral Arteries / pathology*
  • Cerebrovascular Circulation
  • Contrast Media
  • Female
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Spin Labels*
  • Time Factors

Substances

  • Contrast Media
  • Spin Labels

Grants and funding

The research leading to these results has received funding from the German Federal Ministry of Education and Research via the grant “Center for Stroke Research Berlin” (01 EO 0801; http://www.bmbf.de). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.