Atrophy pattern in SCA2 determined by voxel-based morphometry
- 1 October 2003
- journal article
- research article
- Published by Wolters Kluwer Health in NeuroReport
- Vol. 14 (14) , 1799-1802
- https://doi.org/10.1097/00001756-200310060-00008
Abstract
We applied voxel-based morphometry, an indirect volumetric technique, to MRI volumes of patients carrying the spinocerebellar ataxia type 2 mutation to determine patterns of brain atrophy. Nine patients were compared to 27 controls matched for age, sex and handedness. An optimised voxel-based morphometry protocol was used for pre-processing to minimize systematic bias. We observed significant volume loss in the cerebellar hemispheres, vermis, pons, mesencephalon and thalamus. Also affected were several supratentorial areas such as the right orbito-frontal cortex, right temporo-mesial cortex and the primary sensorimotor cortex bilaterally. The volumetric changes of cerebellar hemispheres were inversely correlated to cerebellar symptoms rated by a cerebellar ataxia scale. Two mechanisms could contribute to the observed cortical atrophy. It could be either the result of primary supratentorial degeneration as part of the disease process and/or secondary atrophy due to cerebellar deafferentation.Keywords
This publication has 24 references indexed in Scilit:
- Cognitive deficits in spinocerebellar ataxia type 1, 2, and 3Zeitschrift für Neurologie, 2003
- Cognitive findings in spinocerebellar ataxia type 2: relationship to genetic and clinical variablesJournal of the Neurological Sciences, 2002
- Cognitive deficits in spinocerebellar ataxia 2Brain, 1999
- Molecular and Clinical Correlations in Spinocerebellar Ataxia 2: A Study of 32 FamiliesHuman Molecular Genetics, 1997
- Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeatsNature Genetics, 1996
- Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECTNature Genetics, 1996
- Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2Nature Genetics, 1996
- Autosomal dominant cerebellar ataxia type I Clinical features and MRI in families with SCA1, SCA2 and SCA3Brain, 1996
- Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies)Brain, 1995
- Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23–24.1Nature Genetics, 1993