TY - JOUR
T1 - Brain structure in asymptomatic FMR1 premutation carriers at risk for fragile X-associated tremor/ataxia syndrome
AU - Battistella, Giovanni
AU - Niederhauser, Julien
AU - Fornari, Eleonora
AU - Hippolyte, Loyse
AU - Gronchi Perrin, Aline
AU - Lesca, Gaetan
AU - Forzano, Francesca
AU - Hagmann, Patric
AU - Vingerhoets, Francois J.G.
AU - Draganski, Bogdan
AU - Maeder, Philippe
AU - Jacquemont, Sébastien
N1 - Funding Information:
The authors are indebted to all the families and individuals who participated in this study. Special thanks to the UK Fragile X Society and the Association Nationale du Syndrome de l'X Fragile, le Goéland for their precious collaboration. The study was supported by the Swiss National Fund 320030_122674 , Centre d'Imagerie BioMédicale (CIBM) of the University of Lausanne (UNIL) , the Swiss Federal Institute of Technology Lausanne (EPFL) , the University of Geneva (UniGe) , the Centre Hospitalier Universitaire Vaudois (CHUV) , the Hôpitaux Universitaires de Genève (HUG) , and the Leenaards and the Jeantet Foundations . The authors acknowledge Marina Grasso for her contribution in the recruitment of the participants and for the DNA testing. The authors also acknowledge Professor Gunnar Krueger for his support with setting up the MR sequences, and Dr C. Wider for his input in the manuscript editing. This work was supported by the Swiss National Fund 320030_122674 and the Synapsis Foundation, Switzerland. PH was supported by the Leenaards Foundation . SJ was supported by a grant from the Faculté de Biologie et de Médecine, Relève Académique .
PY - 2013/6
Y1 - 2013/6
N2 - 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.
AB - 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.
KW - DTI
KW - FXTAS
KW - Genetics
KW - Premutation
KW - Volumetric MRI
UR - http://www.scopus.com/inward/record.url?scp=84875274487&partnerID=8YFLogxK
U2 - 10.1016/j.neurobiolaging.2012.12.001
DO - 10.1016/j.neurobiolaging.2012.12.001
M3 - Article
C2 - 23298734
AN - SCOPUS:84875274487
SN - 0197-4580
VL - 34
SP - 1700
EP - 1707
JO - Neurobiology of Aging
JF - Neurobiology of Aging
IS - 6
ER -