Regional Brain and Spinal Cord Volume Loss in Spinocerebellar Ataxia Type 3

  • Jennifer Faber*
  • , Tamara Schaprian
  • , Koyak Berkan
  • , Kathrin Reetz
  • , Marcondes Cavalcante Franca
  • , Thiago Junqueira Ribeiro Rezende
  • , Jiang Hong
  • , Weihua Liao
  • , Bart Warrenburg
  • , Judith Gaalen
  • , Alexandra Durr
  • , Fanny Mochel
  • , Paola Giunti
  • , Hector Garcia-Moreno
  • , Ludger Schoels
  • , Holger Hengel
  • , Matthis Synofzik
  • , Benjamin Bender
  • , Gulin Oz
  • , James Joers
  • Jereon J. Vries, Jun-Suk Kang, Dagmar Timmann-Braun, Heike Jacobi, Jon Infante, Richard Joules, Sandro Romanzetti, Jorn Diedrichsen, Matthias Schmid, Robin Wolz, Thomas Klockgether
*Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    44 Citations (Scopus)
    95 Downloads (Pure)

    Abstract

    Background Given that new therapeutic options for spinocerebellar ataxias are on the horizon, there is a need for markers that reflect disease-related alterations, in particular, in the preataxic stage, in which clinical scales are lacking sensitivity.

    Objective The objective of this study was to quantify regional brain volumes and upper cervical spinal cord areas in spinocerebellar ataxia type 3 in vivo across the entire time course of the disease.

    Methods We applied a brain segmentation approach that included a lobular subsegmentation of the cerebellum to magnetic resonance images of 210 ataxic and 48 preataxic spinocerebellar ataxia type 3 mutation carriers and 63 healthy controls. In addition, cervical cord cross-sectional areas were determined at 2 levels.

    Results The metrics of cervical spinal cord segments C3 and C2, medulla oblongata, pons, and pallidum, and the cerebellar anterior lobe were reduced in preataxic mutation carriers compared with controls. Those of cervical spinal cord segments C2 and C3, medulla oblongata, pons, midbrain, cerebellar lobules crus II and X, cerebellar white matter, and pallidum were reduced in ataxic compared with nonataxic carriers. Of all metrics studied, pontine volume showed the steepest decline across the disease course. It covaried with ataxia severity, CAG repeat length, and age. The multivariate model derived from this analysis explained 46.33% of the variance of pontine volume.

    Conclusion Regional brain and spinal cord tissue loss in spinocerebellar ataxia type 3 starts before ataxia onset. Pontine volume appears to be the most promising imaging biomarker candidate for interventional trials that aim at slowing the progression of spinocerebellar ataxia type 3. (c) 2021 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society

    Original languageEnglish
    Pages (from-to)2273-2281
    Number of pages11
    JournalMovement Disorders
    Volume36
    Issue number10
    Early online date5-May-2021
    DOIs
    Publication statusPublished - Oct-2021

    Keywords

    • spinocerebellar ataxia
    • MRI
    • volumetry
    • biomarker

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