Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA

PLoS One. 2016 Apr 18;11(4):e0152439. doi: 10.1371/journal.pone.0152439. eCollection 2016.

Abstract

Purpose: The mechanisms underlying the topography of motor deficits in spinal muscular atrophy (SMA) remain unknown. We investigated the profile of spinal cord atrophy (SCA) in SMN1-linked SMA, and its correlation with the topography of muscle weakness.

Materials and methods: Eighteen SMN1-linked SMA patients type III/V and 18 age/gender-matched healthy volunteers were included. Patients were scored on manual muscle testing and functional scales. Spinal cord was imaged using 3T MRI system. Radial distance (RD) and cord cross-sectional area (CSA) measurements in SMA patients were compared to those in controls and correlated with strength and disability scores.

Results: CSA measurements revealed a significant cord atrophy gradient mainly located between C3 and C6 vertebral levels with a SCA rate ranging from 5.4% to 23% in SMA patients compared to controls. RD was significantly lower in SMA patients compared to controls in the anterior-posterior direction with a maximum along C4 and C5 vertebral levels (p-values < 10-5). There were no correlations between atrophy measurements, strength and disability scores.

Conclusions: Spinal cord atrophy in adult SMN1-linked SMA predominates in the segments innervating the proximal muscles. Additional factors such as neuromuscular junction or intrinsic skeletal muscle defects may play a role in more complex mechanisms underlying weakness in these patients.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Case-Control Studies
  • Cervical Cord / metabolism
  • Cervical Cord / pathology*
  • Female
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Muscle Strength / physiology
  • Muscular Atrophy, Spinal / metabolism
  • Muscular Atrophy, Spinal / pathology*
  • Spinal Cord / metabolism
  • Spinal Cord / pathology*
  • Survival of Motor Neuron 1 Protein / genetics*
  • Survival of Motor Neuron 1 Protein / metabolism

Substances

  • Survival of Motor Neuron 1 Protein

Grants and funding

The authors have no support or funding to report.