Grey matter volume correlates of cerebrospinal markers of Alzheimer-pathology in Parkinson's disease and related dementia

被引:52
|
作者
Compta, Yaroslau [1 ]
Ibarretxe-Bilbao, Naroa [2 ,3 ]
Pereira, Joana B. [3 ]
Junque, Carme [3 ]
Bargallo, Nuria [4 ]
Tolosa, Eduardo [1 ]
Valldeoriola, Francesc [1 ]
Munoz, Esteban [1 ]
Camara, Ana [1 ]
Buongiorno, Mariateresa [1 ]
Jose Marti, Maria [1 ]
机构
[1] Hosp Clin Barcelona, Ctr Invest Red Enfermedades Neurodegenerat CIBERN, Inst Invest Biomed August Pi & Sunyer IDIBAPS,ICN, Parkinsons Dis & Movement Disorders Unit,Neurol S, E-08036 Barcelona, Catalonia, Spain
[2] Univ Deusto, Fac Psychol & Educ, Dept Methods & Expt Psychol, Basque Country, Spain
[3] Univ Barcelona, CIBERNED Fac Med, IDIBAPS, Dept Psychiat & Clin Psychobiol, Catalonia, Spain
[4] Hosp Clin Barcelona, Magnet Resonance Unit, Hosp Clin, Neurorradiol Sect,CDI,IDIBAPS, E-08036 Barcelona, Catalonia, Spain
关键词
Parkinson's disease; Dementia; Grey matter volume; Magnetic resonance imaging; Cerebrospinal fluid; tau; Amyloid-beta; VOXEL-BASED MORPHOMETRY; CSF AMYLOID-BETA; COGNITIVE IMPAIRMENT; CEREBRAL ATROPHY; TAU; LEWY; NEUROPATHOLOGY; PROGRESSION; BIOMARKERS; DIAGNOSIS;
D O I
10.1016/j.parkreldis.2012.04.028
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Regional brain grey matter volume (GMV) reductions and abnormal cerebrospinal fluid (CSF) levels of tau and A beta, extensively studied as biomarkers of Alzheimer's disease (AD), have also been reported in Parkinson's disease (PD) and related dementia (PDD). However, the relationship between these CSF and MRI biomarkers in PD and PDD remains unexplored. We studied these associations in 33 PD patients (18 with no dementia [PDND]; 15 fulfilling PDD criteria) and 12 neurologically unimpaired controls, with neuropsychological assessment, CSF ELISA studies, and voxel-based morphometry (VBM) analysis of high-field brain MRI. Neuropsychological assessment showed a gradation in cognitive performance from controls to PDND (significantly worse on visuospatial performance) and then to PDD (more impaired on memory, naming, fluency and visuospatial functions). No CSF-VBM correlations were found in controls or PDND patients. In contrast, in the analysis of both the PDD subgroup and the entire PD (PDND + PDD) sample, we found significant negative CSF-GMV correlations for tau and phospho-tau and significant positive CSF-GMV correlations for A beta in mostly frontal and temporal structures. The correlations in the entire PD sample fitted with a linear model and were thus unlikely to have been driven solely by the PDD subgroup. Additionally, an association between both the CSF markers and the CSF-associated GMV reductions with several neuropsychological functions was found. We interpret that CSF markers of AD pathology are associated with VBM-measures of brain atrophy in PD-related dementia and within the PD cognitive continuum, and deserve further attention as putative biomarkers of cognitive impairment and dementia in PD. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:941 / 947
页数:7
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