Brain structural profile of multiple system atrophy patients with cognitive impairment

被引:0
作者
Eleonora Fiorenzato
Luca Weis
Klaus Seppi
Marco Onofrj
Pietro Cortelli
Stefano Zanigni
Caterina Tonon
Horacio Kaufmann
Timothy Michael Shepherd
Werner Poewe
Florian Krismer
Gregor Wenning
Angelo Antonini
Roberta Biundo
机构
[1] IRCCS San Camillo Hospital Foundation,Parkinson Disease and Movement Disorders Unit
[2] University of Padua,Department of General Psychology
[3] Medical University of Innsbruck,Department of Neurology
[4] “G. d’Annunzio” University,Department of Neuroscience, Imaging and Clinical Sciences
[5] IRCCS Institute of Neurological Sciences of Bologna,Department of Biomedical and Neuromotor Sciences (DIBINEM)
[6] University of Bologna,Functional MR Unit
[7] S. Orsola-Malpighi Hospital,Department of Neurology, Dysautonomia Center
[8] New York University,undefined
来源
Journal of Neural Transmission | 2017年 / 124卷
关键词
Multiple system atrophy (MSA); Cognition; Mini-Mental State Examination (MMSE); Dementia; Neuroimaging; Voxel-based morphometry;
D O I
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学科分类号
摘要
Current consensus diagnostic criteria for multiple system atrophy (MSA) consider dementia a non-supporting feature, although cognitive impairment and even frank dementia are reported in clinical practice. Mini-Mental State Examination (MMSE) is a commonly used global cognitive scale, and in a previous study, we established an MSA-specific screening cut-off score <27 to identify cognitive impairment. Finally, MSA neuroimaging findings suggest the presence of structural alterations in patients with cognitive deficits, although the extent of the anatomical changes is unclear. The aim of our multicenter study is to better characterize anatomical changes associated with cognitive impairment in MSA and to further investigate cortical and subcortical structural differences versus healthy controls (HC). We examined retrospectively 72 probable MSA patients [50 with normal cognition (MSA-NC) and 22 cognitively impaired (MSA-CI) based on MMSE <27] and compared them to 36 HC using gray- and white-matter voxel-based morphometry and fully automated subcortical segmentation. Compared to HC, MSA patients showed widespread cortical (bilateral frontal, occipito-temporal, and parietal areas), subcortical, and white-matter alterations. However, MSA-CI showed only focal volume reduction in the left dorsolateral prefrontal cortex compared with MSA-NC. These results suggest only a marginal contribution of cortical pathology to cognitive deficits. We believe that cognitive dysfunction is driven by focal fronto-striatal degeneration in line with the concept of “subcortical cognitive impairment”.
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页码:293 / 302
页数:9
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