Diffusion tensor imaging and voxel based morphometry study in early progressive supranuclear palsy
Identifieur interne : 001321 ( Main/Exploration ); précédent : 001320; suivant : 001322Diffusion tensor imaging and voxel based morphometry study in early progressive supranuclear palsy
Auteurs : A. Padovani [Italie] ; B. Borroni [Italie] ; S M Brambati [Italie] ; C. Agosti [Italie] ; M. Broli [Italie] ; R. Alonso [Italie] ; P. Scifo [Italie] ; G. Bellelli [Italie] ; A. Alberici [Italie] ; R. Gasparotti [Italie] ; D. Perani [Italie]Source :
- Journal of Neurology, Neurosurgery & Psychiatry [ 0022-3050 ] ; 2006-04.
English descriptors
- KwdEn :
- BADL, basic activities of daily living, CDR, clinical dementia rating scale, CSF, cerebrospinal fluid, DSM-IV, Diagnostic and Statistical Manual of Mental Disorders, fourth edition, DTI, diffusion tensor imaging, FA, fractional anisotropy, FBI, frontal behavioural inventory, FDR, false discovery rate, FWHM, full width at half maximum, GM, grey matter, IADL, instrumental activities of daily living, MMSE, mini-mental state examination, MNI, Montreal Neurological Institute, NPI, neuropsychiatric inventory, PSP, progressive supranuclear palsy, UPDRS, unified Parkinson disease rating scale, VBM, voxel based morphometry, WM, white matter, diffusion tensor imaging, magnetic resonance imaging, progressive supranuclear palsy, voxel based morphometry.
Abstract
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.
Url:
DOI: 10.1136/jnnp.2005.075713
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">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.</div>
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