Quantification of perfusion and permeability in multiple sclerosis: dynamic contrast-enhanced MRI in 3D at 3T

Michael Ingrisch1, Steven Sourbron, Dominik Morhard

  • 1Josef Lissner Laboratory for Biomedical Imaging, Department of Clinical Radiology, University Hospitals Munich-Grosshadern, Ludwig Maximilian University of Munich, Germany. michael.ingrisch@med.uni-muenchen.de

Abstract

Insights

This study shows 3D T1-weighted dynamic contrast-enhanced MRI can quantify blood flow and volume in multiple sclerosis lesions. These findings may help characterize lesion activity and understand brain perfusion changes.

Area of Science:

  • Neuroimaging
  • Radiology
  • Medical Physics

Background:

  • Quantifying cerebral blood flow (CBF), cerebral blood volume (CBV), and blood-brain barrier permeability in multiple sclerosis (MS) lesions is challenging.
  • Accurate assessment is crucial for understanding disease mechanisms and evaluating treatment efficacy.

Purpose of the Study:

  • To investigate the feasibility of 3D T1-weighted dynamic contrast-enhanced (DCE) MRI with 2-compartment modeling.
  • To quantify CBF, CBV, and permeability surface area product (PS) in MS lesions and normal-appearing white matter (NAWM).

Main Methods:

  • 19 MS patients underwent whole-brain DCE-MRI using a 3T scanner with a 3D T1-weighted sequence.
  • Data were acquired every 2.1 seconds for 420 seconds, covering 44 slices.
  • 2-compartment modeling was used to determine CBF, CBV, and PS in contrast-enhancing (CE) lesions, nonenhancing lesions, and NAWM.

Main Results:

  • Perfusion quantification yielded reasonable values in both lesions and NAWM.
  • CE lesions showed significantly higher CBF, CBV, and PS compared to NAWM (P < 0.001).
  • Nonenhancing lesions exhibited significantly increased CBV compared to NAWM (P < 0.05).

Conclusions:

  • 3D T1-weighted DCE-MRI is feasible for quantitative assessment of CBF, CBV, and PS in MS lesions and NAWM.
  • Increased values in CE lesions may indicate inflammatory activity, suggesting potential for lesion characterization.
  • NAWM appears hypoperfused, consistent with prior studies, warranting further validation.