Annals of Clinical and Translational Neurology (Jul 2024)

Gradient of microstructural damage along the dentato‐thalamo‐cortical tract in Friedreich ataxia

  • Sirio Cocozza,
  • Sara Bosticardo,
  • Matteo Battocchio,
  • Louise Corben,
  • Martin Delatycki,
  • Gary Egan,
  • Nellie Georgiou‐Karistianis,
  • Serena Monti,
  • Giuseppe Palma,
  • Chiara Pane,
  • Francesco Saccà,
  • Simona Schiavi,
  • Louisa Selvadurai,
  • Mario Tranfa,
  • Alessandro Daducci,
  • Arturo Brunetti,
  • Ian H. Harding

DOI
https://doi.org/10.1002/acn3.52048
Journal volume & issue
Vol. 11, no. 7
pp. 1691 – 1702

Abstract

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Abstract Objective The dentato‐thalamo‐cortical tract (DTT) is the main cerebellar efferent pathway. Degeneration of the DTT is a core feature of Friedreich ataxia (FRDA). However, it remains unclear whether DTT disruption is spatially specific, with some segments being more impacted than others. This study aimed to investigate microstructural integrity along the DTT in FRDA using a profilometry diffusion MRI (dMRI) approach. Methods MRI data from 45 individuals with FRDA (mean age: 33.2 ± 13.2, Male/Female: 26/19) and 37 healthy controls (mean age: 36.5 ± 12.7, Male/Female:18/19) were included in this cross‐sectional multicenter study. A profilometry analysis was performed on dMRI data by first using tractography to define the DTT as the white matter pathway connecting the dentate nucleus to the contralateral motor cortex. The tract was then divided into 100 segments, and dMRI metrics of microstructural integrity (fractional anisotropy, mean diffusivity and radial diffusivity) at each segment were compared between groups. The process was replicated on the arcuate fasciculus for comparison. Results Across all diffusion metrics, the region of the DTT connecting the dentate nucleus and thalamus was more impacted in FRDA than downstream cerebral sections from the thalamus to the cortex. The arcuate fasciculus was minimally impacted. Interpretation Our study further expands the current knowledge about brain involvement in FRDA, showing that microstructural abnormalities within the DTT are weighted to early segments of the tract (i.e., the superior cerebellar peduncle). These findings are consistent with the hypothesis of DTT undergoing anterograde degeneration arising from the dentate nuclei and progressing to the primary motor cortex.