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

痴呆 基于体素的形态计量学 神经心理学 灰质 萎缩 心理学 脑脊液 病理 白质 医学 认知 神经科学 内科学 听力学 疾病 磁共振成像 放射科
作者
Yaroslau Compta,Naroa Ibarretxe‐Bilbao,Joana B. Pereira,Carme Junqué,Núria Bargalló,Eduardo Tolosa,Francesc Valldeoriola,Esteban Muñoz,Ana Cámara,Maríateresa Buongiorno,Marı́a José Martı́
出处
期刊:Parkinsonism & Related Disorders [Elsevier BV]
卷期号:18 (8): 941-947 被引量:53
标识
DOI:10.1016/j.parkreldis.2012.04.028
摘要

Abstract

Regional brain grey matter volume (GMV) reductions and abnormal cerebrospinal fluid (CSF) levels of τ and Aβ, 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 τ and phospho-τ and significant positive CSF-GMV correlations for Aβ 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.
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