Expanding the Motor Band Sign in Motor Neuron Disease Using 7T MRI: Visualization of Cortical Layer-Dependent Iron

Jaimin S Shah1, Björn Oskarsson1, Xiangzhi Zhou2

  • 1Department of Neurology, Mayo Clinic, Jacksonville, Florida, USA.

Muscle & Nerve
|March 7, 2026
PubMed
Abstract

Insights

The 7T MRI motor band sign (MBS) is a sensitive and specific biomarker for diagnosing motor neuron disease (MND). This imaging marker, particularly its trilaminar appearance, aids in identifying upper motor neuron degeneration.

Area of Science:

  • Neurology
  • Radiology
  • Biomarkers

Background:

  • Established biomarkers for upper motor neuron degeneration in motor neuron disease (MND) are lacking.
  • The motor band sign (MBS) is being investigated as a potential imaging biomarker.

Purpose of the Study:

  • To evaluate the diagnostic value of the 7T MRI MBS in identifying upper motor neuron degeneration in MND.
  • To explore the relationship between the MBS and clinical findings in MND patients.

Main Methods:

  • Retrospective review of 7T MRI scans from patients evaluated for MND or other neurological conditions.
  • Assessment of MBS presence and characteristics (trilaminar appearance) on susceptibility-weighted imaging (SWI).
  • Correlation of MBS findings with clinical variables, including Mayo Upper Motor Neuron Score (UMNS) and plasma neurofilament light chain (pNfL) levels.

Main Results:

  • The MBS was detected in 85.5% of MND patients and 15.5% of non-MND controls, indicating high sensitivity and specificity.
  • A trilaminar MBS appearance, reflecting middle and deep cortical layer involvement, was observed in 70.9% of MND patients, with only one non-MND patient showing this finding.
  • Mayo UMNS, pNfL levels, and age were independently associated with the summed SWI score.

Conclusions:

  • The 7T MRI MBS is a sensitive and specific imaging marker for MND, complementing clinical assessments.
  • The visualization of a trilaminar MBS appearance using 7T MRI may be specific to MND and reflects known histopathological changes.

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