Dorsal root ganglia volume is increased in patients with the Fabry-related GLA variant p.D313Y

J Neurol. 2019 Jun;266(6):1332-1339. doi: 10.1007/s00415-019-09262-8. Epub 2019 Mar 4.

Abstract

Purpose: To examine dorsal root ganglia and proximal nerve segments in patients carrying the Fabry-related GLA-gene variant p.D313Y in comparison to patients with classical Fabry mutations and healthy controls by morphometric and functional magnetic resonance neurography.

Methods: This prospective multicenter study examines the lumbosacral dorsal root ganglia and sciatic nerve in 11 female p.D313Y patients by a standardized magnetic resonance neurography protocol at 3 T. Volumes of dorsal root ganglia L3 to S2, permeability of dorsal root ganglia L5 and S1, and spinal nerve L5 as well as cross-sectional area of the sciatic nerve were assessed and compared to 10 females carrying a classical Fabry mutation and 16 healthy female controls.

Results: Compared to healthy controls, dorsal root ganglia volumes of p.D313Y females were enlarged by 53% (L3), 48% (L4), 43% (L5), 57% (S1) (p < 0.001), and 55% (S2) (p < 0.05), but less pronounced compared to females carrying a classical Fabry mutation. Compared to healthy controls, p.D313Y patients showed no changes of dorsal root ganglia vascular permeability, while patients with a classical Fabry mutation showed a distinct decrease (p < 0.05). Sciatic nerve cross-sectional area was mildly increased by 6% in p.D313Y as well as in classical Fabry patients (p < 0.05).

Conclusions: Patients carrying the GLA-gene variant p.D313Y show distinctly enlarged dorsal root ganglia, while vascular permeability remains within normal limits. Overall, these alterations partially share characteristics commonly seen in patients with a mutation causing classical FD. This suggests that p.D313Y causes a potentially treatable condition resembling an early stage of Fabry disease.

Keywords: Dorsal root ganglia; Fabry disease; Magnetic resonance neurography; Neuropathic pain; Peripheral neuropathy.

Publication types

  • Multicenter Study

MeSH terms

  • Adult
  • Aged
  • Capillary Permeability / physiology
  • Fabry Disease / genetics
  • Female
  • Ganglia, Spinal / diagnostic imaging
  • Ganglia, Spinal / pathology*
  • Ganglia, Spinal / physiopathology
  • Humans
  • Magnetic Resonance Imaging
  • Middle Aged
  • Mutation
  • Peripheral Nervous System Diseases* / genetics
  • Peripheral Nervous System Diseases* / pathology
  • Peripheral Nervous System Diseases* / physiopathology
  • Prospective Studies
  • Sciatic Nerve / diagnostic imaging
  • Sciatic Nerve / pathology*
  • Sciatic Nerve / physiopathology
  • Young Adult
  • alpha-Galactosidase / genetics*

Substances

  • GLA protein, human
  • alpha-Galactosidase