Long-term follow-up of acute partial transverse myelitis

Bertrand Bourre1, Hélène Zéphir, Jean-Claude Ongagna

  • 1Service de Neurologie, Hôpital Charles Nicolle, 1 rue de Germont, Rouen Cedex, France. bertrandbourre@gmail.com

Archives of Neurology
|March 14, 2012
PubMed
Abstract

Insights

Acute partial transverse myelitis (APTM) can be an early sign of multiple sclerosis (MS). Abnormal brain MRI and CSF oligoclonal bands predict MS conversion, but not long-term disability.

Area of Science:

  • Neurology
  • Neuroimmunology
  • Clinical Neuroscience

Background:

  • Acute partial transverse myelitis (APTM) is a neurological condition that may herald multiple sclerosis (MS) or be a standalone event.
  • Understanding the prognosis of APTM is crucial for patient management and predicting long-term outcomes.

Purpose of the Study:

  • To assess the risk of conversion from APTM to MS.
  • To evaluate factors influencing long-term disability in APTM patients.
  • To identify prognostic indicators for disability progression.

Main Methods:

  • A cohort of 85 patients with no prior neurological history experiencing APTM was followed for over 100 months.
  • Data collected included demographics, clinical status, cerebrospinal fluid (CSF) analysis, brain and spinal cord MRI, and visual evoked potentials.
  • Statistical analysis identified predictive factors for MS conversion.

Main Results:

  • Over 60% of patients converted to MS, with a mean disability score indicating mild to moderate impairment.
  • Presence of CSF oligoclonal bands (92% in MS converters) and brain MRI lesions (87% in MS converters) were significantly higher in those who developed MS.
  • CSF oligoclonal bands and brain MRI lesions were independent predictors of MS conversion.

Conclusions:

  • Abnormal brain MRI findings and CSF oligoclonal bands are significant predictors of conversion to MS after an initial APTM event.
  • No specific clinical, biological, or MRI factor at the onset of APTM could predict the level of long-term disability.

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