Analysis of prognostic factors associated with longitudinally extensive transverse myelitis

Mult Scler. 2013 May;19(6):742-8. doi: 10.1177/1352458512461968. Epub 2012 Oct 4.

Abstract

Objective: The aim of this study is to report the clinical profile and outcome of longitudinally extensive transverse myelitis (LETM).

Methods: We prospectively studied adult patients who presented with LETM from January 2008 to December 2011. Information on demographic, clinical course, magnetic resonance imaging (MRI) and outcome was collected. HLA-DRB1 genotype was compared with those of 225 normal controls and patients with MS (228) and neuromyelitis optica (NMO) (22).

Results: In total, 23 patients (16 female) with a median age of 44.5 years (range: 20-77 years) were included. Most (74%) had moderate-severe disability at nadir (48% non-ambulatory), normal/non-multiple sclerosis (MS) brain MRI (96%) and a median MRI cord lesion of 5 vertebral segments (range: 3-19). Laboratory analysis showed cerebrospinal fluid pleocytosis (45%), NMO-IgG (9%), antinuclear antibodies (70%), and genotype HLA-DRB1*13 (57%). The frequency of DRB1*13 genotype was higher compared with controls (p=0.002), MS (p=0.001) and NMO (p=0.003) patients. After a median follow-up of 32 months, one patient converted to MS, two had relapsing LETM with NMO-IgG, and 20 remained as idiopathic with recurrences in four (20%). Twelve (52%) patients recovered with minimal disability (Expanded Disability Status Scale (EDSS) ≤2.5) and three (13%) remained wheelchair dependent. Disability at nadir was associated with the final outcome and extension of the spinal cord lesion with risk of recurrence. Recurrence was not associated with worse outcome.

Conclusions: Inflammatory LETM is mostly idiopathic with a good outcome. It includes a relatively homogenous group of patients with an overrepresentation of the HLA-DRB1*13 genotype. EDSS at nadir is a predictor of the final outcome and extension of the myelitis of the recurrence risk.

Keywords: HLA; MRI; Transverse myelitis; multiple sclerosis; neuromyelitis optica.

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antibodies, Antinuclear / cerebrospinal fluid*
  • Biomarkers / cerebrospinal fluid
  • Brain* / immunology
  • Brain* / pathology
  • Brain* / physiopathology
  • Case-Control Studies
  • Disability Evaluation
  • Disease Progression
  • Female
  • Gene Frequency
  • Genotype
  • HLA-DRB1 Chains / genetics*
  • Humans
  • Leukocytosis / cerebrospinal fluid
  • Leukocytosis / diagnosis
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Myelitis, Transverse / cerebrospinal fluid
  • Myelitis, Transverse / diagnosis*
  • Myelitis, Transverse / genetics
  • Myelitis, Transverse / immunology
  • Myelitis, Transverse / pathology
  • Myelitis, Transverse / physiopathology
  • Myelitis, Transverse / therapy
  • Phenotype
  • Predictive Value of Tests
  • Prospective Studies
  • Recurrence
  • Spain
  • Spinal Cord* / immunology
  • Spinal Cord* / pathology
  • Spinal Cord* / physiopathology
  • Time Factors
  • Treatment Outcome
  • Young Adult

Substances

  • Antibodies, Antinuclear
  • Biomarkers
  • HLA-DRB1 Chains
  • HLA-DRB1*13 antigen