Pattern of Cerebellar Atrophy in Friedreich’s Ataxia—Using the SUIT Template

被引:0
|
作者
Tobias Lindig
Benjamin Bender
Vinod J. Kumar
Till-Karsten Hauser
Wolfgang Grodd
Bettina Brendel
Jennifer Just
Matthis Synofzik
Uwe Klose
Klaus Scheffler
Ulrike Ernemann
Ludger Schöls
机构
[1] University Hospital Tübingen,Department of Diagnostic and Interventional Neuroradiology
[2] Max Planck Institute for Biological Cybernetics,High
[3] University Hospital Tübingen,Field MR Center
[4] University of Tübingen,Department of Psychiatry and Psychotherapy
[5] Eberhard Karls University,Institute of Clinical Epidemiology and applied Biometry (IKEaB)
[6] German Research Center for Neurodegenerative Diseases (DZNE),Department of Neurology and Hertie Institute for Clinical Brain Research
[7] University Hospital Tübingen,Department of Biomedical Magnetic Resonance
来源
The Cerebellum | 2019年 / 18卷
关键词
Cerebellum; Dentate nucleus; FRDA; MRI; SUIT; VBM; Volumetry;
D O I
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中图分类号
学科分类号
摘要
Whole-brain voxel-based morphometry (VBM) studies revealed patterns of patchy atrophy within the cerebellum of Friedreich’s ataxia patients, missing clear clinico-anatomic correlations. Studies so far are lacking an appropriate registration to the infratentorial space. To circumvent these limitations, we applied a high-resolution atlas template of the human cerebellum and brainstem (SUIT template) to characterize regional cerebellar atrophy in Friedreich’s ataxia (FRDA) on 3-T MRI data. We used a spatially unbiased voxel-based morphometry approach together with T2-based manual segmentation, T2 histogram analysis, and atlas generation of the dentate nuclei in a representative cohort of 18 FRDA patients and matched healthy controls. We demonstrate that the cerebellar volume in FRDA is generally not significantly different from healthy controls but mild lobular atrophy develops beyond normal aging. The medial parts of lobule VI, housing the somatotopic representation of tongue and lips, are the major site of this lobular atrophy, which possibly reflects speech impairment. Extended white matter affection correlates with disease severity across and beyond the cerebellar inflow and outflow tracts. The dentate nucleus, as a major site of cerebellar degeneration, shows a mean volume loss of about 30%. Remarkably, not the atrophy but the T2 signal decrease of the dentate nuclei highly correlates with disease duration and severity.
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页码:435 / 447
页数:12
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