Brain structure in asymptomatic FMR1 premutation carriers at risk for fragile X-associated tremor/ataxia syndrome

Giovanni Battistella, Julien Niederhauser, Eleonora Fornari, Loyse Hippolyte, Aline Gronchi Perrin, Gaetan Lesca, Francesca Forzano, Patric Hagmann, Francois J.G. Vingerhoets, Bogdan Draganski, Philippe Maeder, Sébastien Jacquemont

Research output: Contribution to journalArticlepeer-review

50 Scopus citations

Abstract

Fragile X-associated tremor/ataxia syndrome (FXTAS), a late-onset movement disorder affecting FMR1 premutation carriers, is associated with cerebral and cerebellar lesions. The aim of this study was to test whether computational anatomy can detect similar patterns in asymptomatic FMR1 premutation carriers (mean age 46.7 years) with qualitatively normal -appearing grey and white matter on brain MRI. We used a multimodal imaging protocol to characterize brain anatomy by automated assessment of gray matter volume and white matter properties. Structural changes in the hippocampus and in the cerebellar motor network with decreased gray matter volume in lobule VI and white matter alterations of the corresponding afferent projections through the middle cerebellar peduncles are demonstrated. Diffuse subcortical white matter changes in both hemispheres, without corresponding gray matter alterations, are only identified through age × group interactions. We interpret the hippocampal fimbria and cerebellar changes as early alterations with a possible neurodevelopmental origin. In contrast, progression of the diffuse cerebral hemispheric white matter changes suggests a neurodegenerative process, leading to late-onset lesions, which may mark the imminent onset of FXTAS.

Original languageEnglish
Pages (from-to)1700-1707
Number of pages8
JournalNeurobiology of Aging
Volume34
Issue number6
DOIs
StatePublished - Jun 2013
Externally publishedYes

Keywords

  • DTI
  • FXTAS
  • Genetics
  • Premutation
  • Volumetric MRI

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