在没有痴呆的个体中,灰质网络特性与脑脊液p-tau 181水平和淀粉样蛋白状态有明显的关联

IF 1.7 Q3 CLINICAL NEUROLOGY Aging brain Pub Date : 2022-01-01 DOI:10.1016/j.nbas.2022.100054
Luigi Lorenzini , Silvia Ingala , Viktor Wottschel , Alle Meije Wink , Henk JMM Mutsaerts , Sven Haller , Kaj Blennow , John T. O'Brien , B. Giovanni Frisoni , Gael Chételat , Pierre Payoux , Pablo Martinez-Lage , Adam Waldman , Joanna Wardlaw , Craig Ritchie , Juan Domingo Gispert , Pieter Jelle Visser , Philip Scheltens , Frederik Barkhof , Betty M. Tijms
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摘要

在阿尔茨海默病的早期阶段,灰质网络随着淀粉样蛋白的积累而改变,并与阿尔茨海默病的整个谱系的衰退有关。目前尚不清楚灰质网络异常在多大程度上与过度磷酸化的tau蛋白(p-tau)相关。我们研究了来自欧洲预防阿尔茨海默氏痴呆(EPAD)队列的非痴呆参与者脑脊液(CSF) p-tau181与灰质网络的关系,并研究了淀粉样蛋白和认知状态的依赖性。从基线结构3D T1w MRI中提取灰质网络。P-tau181和β用罗氏cobas Elecsys系统测定。我们研究了脑脊液生物标志物水平与几个网络图属性的关联。我们进一步研究了p-tau 181和网络测量的关系是否依赖于淀粉样蛋白状态和认知阶段(CDR)。我们在区域层面上重复了这些网络属性分析,在自动解剖标记(AAL)图谱中定义的116个区域中,我们平均了每个区域的局部网络值。淀粉样蛋白阳性与较高的网络大小和中间度中心性以及较低的γ、聚类和小世界系数相关。较高的CSF p-tau 181水平与较低的中间度中心性、路径长度和λ系数相关(p均为 < 0.01)。p-tau181、淀粉样蛋白状态和CDR之间在路径长度、lambda和聚类方面存在三方相互作用(p均为 < 0.05):认知未受损的淀粉样蛋白阴性参与者的路径长度和lambda值较低,CSF p-tau181水平较高。认知受损的淀粉样蛋白阳性参与者表现出较低的聚类系数与较高的CSF p-tau181水平相关。我们的研究结果表明,灰质网络聚类系数的改变是AD的早期特异性事件。
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Gray matter network properties show distinct associations with CSF p-tau 181 levels and amyloid status in individuals without dementia

Gray matter networks are altered with amyloid accumulation in the earliest stage of AD, and are associated with decline throughout the AD spectrum. It remains unclear to what extent gray matter network abnormalities are associated with hyperphosphorylated-tau (p-tau). We studied the relationship of cerebrospinal fluid (CSF) p-tau181 with gray matter networks in non-demented participants from the European Prevention of Alzheimer’s Dementia (EPAD) cohort, and studied dependencies on amyloid and cognitive status. Gray matter networks were extracted from baseline structural 3D T1w MRI. P-tau181 and abeta were measured with the Roche cobas Elecsys System. We studied the associations of CSF biomarkers levels with several network’s graph properties. We further studied whether the relationships of p-tau 181 and network measures were dependent on amyloid status and cognitive stage (CDR). We repeated these analyses for network properties at a regional level, where we averaged local network values across cubes within each of 116 areas as defined by the automated anatomical labeling (AAL) atlas. Amyloid positivity was associated with higher network size and betweenness centrality, and lower gamma, clustering and small-world coefficients. Higher CSF p-tau 181 levels were related to lower betweenness centrality, path length and lambda coefficients (all p < 0.01). Three-way interactions between p-tau181, amyloid status and CDR were found for path length, lambda and clustering (all p < 0.05): Cognitively unimpaired amyloid-negative participants showed lower path length and lambda values with higher CSF p-tau181 levels. Amyloid-positive participants with impaired cognition demonstrated lower clustering coefficients in association to higher CSF p-tau181 levels.

Our results suggest that alterations in gray matter network clustering coefficient is an early and specific event in AD.

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Aging brain
Aging brain Neuroscience (General), Geriatrics and Gerontology
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