MRI to detect and localize the area postrema in multiple sclerosis: The role of 3D-DIR and 3D-FLAIR

Valentine Farges1, Salem Hannoun2, Théo Benini1

  • 1Faculty of Medicine, Claude Bernard Lyon 1 University, Lyon, France.

Abstract

Insights

Detecting the area postrema (AP) is crucial for diagnosing neuromyelitis optica spectrum disorder (NMOSD). 3D-double inversion recovery (3DDIR) and 3D-fluid-attenuated inversion recovery (3DFLAIR) MRI sequences, particularly in the axial plane, are most effective for AP visualization.

Area of Science:

  • Neuroimaging
  • Radiology
  • Neurology

Background:

  • The area postrema (AP) is a key structure affected in AP syndrome, often linked to autoimmune diseases like neuromyelitis optica spectrum disorder (NMOSD).
  • Accurate AP detection is vital for diagnosing challenging NMOSD cases.

Purpose of the Study:

  • To determine the optimal cerebral MRI sequences and imaging planes for detecting the area postrema (AP).
  • To improve the diagnostic accuracy of neuromyelitis optica spectrum disorder (NMOSD) by enhancing AP visualization.

Main Methods:

  • Analysis of 3DT1, 2DT2, 3D-fluid-attenuated inversion recovery (3DFLAIR), and 3D-double inversion recuperation (3DDIR) MRI sequences.
  • Scoring of image quality and AP detection ability across different planes.
  • Evaluation in three patient groups with varying MRI sequence availability.

Main Results:

  • The area postrema (AP) was undetectable on 3DT1 and 2DT2 sequences.
  • AP detection rates were 87% for 3DFLAIR and 100% for 3DDIR in the axial plane.
  • 3DDIR and 3DFLAIR sequences demonstrated high efficacy in AP visualization.

Conclusions:

  • 3DDIR and 3DFLAIR MRI sequences are essential additions to NMOSD diagnostic protocols for AP assessment.
  • The axial plane is the most effective for identifying the area postrema (AP).
  • Optimized MRI protocols can aid in the diagnosis of difficult NMOSD cases.