Magnetization transfer ratio quantifies polyneuropathy in hereditary transthyretin amyloidosis

Ann Clin Transl Neurol. 2020 May;7(5):799-807. doi: 10.1002/acn3.51049. Epub 2020 Apr 25.

Abstract

Objective: To quantify peripheral nerve lesions in symptomatic and asymptomatic hereditary transthyretin amyloidosis with polyneuropathy (ATTRv-PNP) by analyzing the magnetization transfer ratio (MTR) of the sciatic nerve, and to test its potential as a novel biomarker for macromolecular changes.

Methods: Twenty-five patients with symptomatic ATTRv-PNP, 30 asymptomatic carriers of the mutant transthyretin gene (mutTTR), and 20 age-/sex-matched healthy controls prospectively underwent magnetization transfer contrast imaging at 3 Tesla. Two axial three-dimensional gradient echo sequences with and without an off-resonance saturation rapid frequency pulse were conducted at the right distal thigh. Sciatic nerve regions of interest were manually drawn on 10 consecutive axial slices in the images without off-resonance saturation, and then transferred to the corresponding slices that were generated by the sequence with the off-resonance saturation pulse. Subsequently, the MTR and cross-sectional area (CSA) of the sciatic nerve were evaluated. Detailed neurologic and electrophysiologic examinations were conducted in all ATTRv-PNP patients and mutTTR-carriers.

Results: Sciatic nerve MTR and CSA reliably differentiated between ATTRv-PNP, mutTTR-carriers, and controls. MTR was lower in ATTRv-PNP (26.4 ± 0.7; P < 0.0001) and in mutTTR-carriers (32.6 ± 0.8; P = 0.0005) versus controls (39.4 ± 2.1), and was also lower in ATTRv-PNP versus mutTTR-carriers (P = 0.0009). MTR correlated negatively with the NIS-LL and positively with CMAPs and SNAPs. CSA was higher in ATTRv-PNP (34.3 ± 1.7 mm3 ) versus mutTTR-carriers (26.0 ± 1.1 mm3 ; P = 0.0005) and versus controls (20.4 ± 1.2 mm3 ; P < 0.0001). CSA was also higher in mutTTR-carriers versus controls.

Interpretation: MTR is a novel imaging marker that can quantify macromolecular changes in ATTRv-PNP and differentiate between symptomatic ATTRv-PNP and asymptomatic mutTTR-carriers and correlates with electrophysiology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Amyloid Neuropathies, Familial / complications
  • Amyloid Neuropathies, Familial / diagnostic imaging*
  • Amyloid Neuropathies, Familial / genetics
  • Amyloid Neuropathies, Familial / pathology
  • Biomarkers
  • Case-Control Studies
  • Female
  • Heterozygote
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Polyneuropathies / diagnostic imaging*
  • Polyneuropathies / etiology
  • Polyneuropathies / pathology
  • Prealbumin / genetics
  • Prospective Studies
  • Sciatic Nerve / diagnostic imaging*
  • Sciatic Nerve / pathology*
  • Young Adult

Substances

  • Biomarkers
  • Prealbumin
  • TTR protein, human

Supplementary concepts

  • Amyloidosis, Hereditary, Transthyretin-Related

Grants and funding

This work was funded by Deutsche Forschungsgemeinschaft grants SFB 1118 and SFB 1158; Universität Heidelberg grant ; Alnylam Pharmaceuticals grant ; Dietmar Hopp Foundation grant ; Siemens Healthcare grant ; European Union grant .