Centrally-located transverse myelitis would facilitate the differentiation of NMOSD and MOG-AD from MS

Masoud Etemadifar1, Mehri Salari2, Mohammad Reza Etemadifar1

  • 1Department of Functional Neurosurgery, Medical School, Isfahan University of Medical Sciences, Isfahan, Iran.

Abstract

Insights

Centrally located lesions on spinal MRI are more sensitive and specific for diagnosing neuromyelitis optica spectrum disorder (NMOSD) and MOG-AD than long extending transverse myelitis (LETM). This finding aids in distinguishing these conditions from multiple sclerosis (MS).

Area of Science:

  • Neuroimmunology
  • Neuroradiology
  • Clinical Neurology

Background:

  • Differentiating neuromyelitis optica spectrum disorder (NMOSD) and Myelin oligodendrocyte glycoprotein antibody disease (MOG-AD) from multiple sclerosis (MS) is crucial, as MS therapies can worsen NMOSD and MOG-AD.
  • Current NMOSD diagnostic criteria include evidence of long extending transverse myelitis (LETM) on MRI.
  • Centrally located lesions on spinal MRI may offer improved diagnostic accuracy for NMOSD and MOG-AD.

Purpose of the Study:

  • To investigate the association between centrally located lesions at disease onset and NMOSD diagnosis.
  • To compare the diagnostic utility of centrally located lesions versus LETM in differentiating NMOSD and MOG-AD from MS.

Main Methods:

  • Retrospective review of 102 medical records from patients presenting with cervical cord lesions at the Isfahan MS clinic.
  • Selection of 17 MS, 23 NMOSD, and 6 MOG-AD patients for detailed analysis.
  • Collection and analysis of demographic, clinical, and MRI data, focusing on the characteristics of cervical cord lesions at disease onset.

Main Results:

  • A significant association was found between NMOSD diagnosis and the presence of centrally located lesions (CLTM), LETM, and intermediate to high axial cord expansion (all P < 0.001).
  • CLTM and LETM were also observed in MOG-AD patients.
  • CLTM demonstrated higher sensitivity (95.65%) and specificity (69.56%) for NMOSD diagnosis compared to LETM (sensitivity: 78.26%, specificity: 43.47%).

Conclusions:

  • The presence and characteristics of transverse myelitis lesions, including centrality, location, and expansion, alongside LETM, are vital for accurate NMOSD and MOG-AD diagnosis.
  • Incorporating lesion centrality into diagnostic criteria may enhance the differentiation of NMOSD and MOG-AD from MS.

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