Diffusion tensor imaging and voxel based morphometry study in early progressive supranuclear palsy

Background: A comprehensive characterisation of grey and white matter changes in progressive supranuclear palsy (PSP), the second most common extrapyramidal syndrome after Parkinson disease, is still not available. Objective: To evaluate grey and white matter changes in mild PSP patients by voxel ba...

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Published inJournal of neurology, neurosurgery and psychiatry Vol. 77; no. 4; pp. 457 - 463
Main Authors Padovani, A, Borroni, B, Brambati, S M, Agosti, C, Broli, M, Alonso, R, Scifo, P, Bellelli, G, Alberici, A, Gasparotti, R, Perani, D
Format Journal Article
LanguageEnglish
Published London BMJ Publishing Group Ltd 01.04.2006
BMJ
BMJ Publishing Group LTD
BMJ Group
Subjects
CDR
CSF
DTI
FBI
FDR
MNI
NPI
PSP
VBM
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Summary:Background: A comprehensive characterisation of grey and white matter changes in progressive supranuclear palsy (PSP), the second most common extrapyramidal syndrome after Parkinson disease, is still not available. Objective: To evaluate grey and white matter changes in mild PSP patients by voxel based morphometry (VBM) and diffusion tensor imaging (DTI), respectively. Methods: 14 mild PSP patients and 14 healthy controls entered the study and underwent a clinical and neuropsychological evaluation according with a standardised assessment. Each subject had a structural magnetic resonance imaging (MRI) study. Processing analysis of MRI data was carried out according to optimised VBM and fractional anisotropy was determined. Results: Compared with the controls, in PSP patients VBM analysis showed a significant clusters of reduced grey matter in premotor cortex, frontal operculum, anterior insula, hippocampus, and parahippocampal gyrus, bilaterally. With regard to subcortical brain regions, the pulvinar, dorsomedial and anterior nuclei of the thalamus, and superior and inferior culliculum were affected bilaterally. A bilateral decrease in fractional anisotropy in superior longitudinal fasciculus, anterior part of corpus callosum, arcuate fascicolus, posterior thalamic radiations, and internal capsule, probably involving the cortico-bulbar tracts, was present in PSP patients. Conclusions: These data provide evidence for both grey and white matter degeneration in PSP from the early disease stage. These structural changes suggest that atrophy of cortical and subcortical structures and neurodegeneration of specific fibre tracts contribute to neurological deficits in PSP.
Bibliography:Correspondence to:
 Dr Alessandro Padovani
 Clinica Neurologica, Università degli Studi di Brescia, Pza Spedali Civili, 1-25100 Brescia, Italy; padovani@med.unibs.it
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ISSN:0022-3050
1468-330X
DOI:10.1136/jnnp.2005.075713