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tau 病理学认知和大脑弹性的决定因素:一项纵向分析。

Determinants of cognitive and brain resilience to tau pathology: a longitudinal analysis.

机构信息

Alzheimer Center Amsterdam, Neurology, Vrije Universiteit Amsterdam, Amsterdam UMC location VUmc, 1081 HZ Amsterdam, The Netherlands.

Amsterdam Neuroscience, Neurodegeneration, 1081 HV Amsterdam, The Netherlands.

出版信息

Brain. 2023 Sep 1;146(9):3719-3734. doi: 10.1093/brain/awad100.

Abstract

Mechanisms of resilience against tau pathology in individuals across the Alzheimer's disease spectrum are insufficiently understood. Longitudinal data are necessary to reveal which factors relate to preserved cognition (i.e. cognitive resilience) and brain structure (i.e. brain resilience) despite abundant tau pathology, and to clarify whether these associations are cross-sectional or longitudinal. We used a longitudinal study design to investigate the role of several demographic, biological and brain structural factors in yielding cognitive and brain resilience to tau pathology as measured with PET. In this multicentre study, we included 366 amyloid-β-positive individuals with mild cognitive impairment or Alzheimer's disease dementia with baseline 18F-flortaucipir-PET and longitudinal cognitive assessments. A subset (n = 200) additionally underwent longitudinal structural MRI. We used linear mixed-effects models with global cognition and cortical thickness as dependent variables to investigate determinants of cognitive resilience and brain resilience, respectively. Models assessed whether age, sex, years of education, APOE-ε4 status, intracranial volume (and cortical thickness for cognitive resilience models) modified the association of tau pathology with cognitive decline or cortical thinning. We found that the association between higher baseline tau-PET levels (quantified in a temporal meta-region of interest) and rate of cognitive decline (measured with repeated Mini-Mental State Examination) was adversely modified by older age (Stβinteraction = -0.062, P = 0.032), higher education level (Stβinteraction = -0.072, P = 0.011) and higher intracranial volume (Stβinteraction = -0.07, P = 0.016). Younger age, higher education and greater cortical thickness were associated with better cognitive performance at baseline. Greater cortical thickness was furthermore associated with slower cognitive decline independent of tau burden. Higher education also modified the negative impact of tau-PET on cortical thinning, while older age was associated with higher baseline cortical thickness and slower rate of cortical thinning independent of tau. Our analyses revealed no (cross-sectional or longitudinal) associations for sex and APOE-ε4 status on cognition and cortical thickness. In this longitudinal study of clinically impaired individuals with underlying Alzheimer's disease neuropathological changes, we identified education as the most robust determinant of both cognitive and brain resilience against tau pathology. The observed interaction with tau burden on cognitive decline suggests that education may be protective against cognitive decline and brain atrophy at lower levels of tau pathology, with a potential depletion of resilience resources with advancing pathology. Finally, we did not find major contributions of sex to brain nor cognitive resilience, suggesting that previous links between sex and resilience might be mainly driven by cross-sectional differences.

摘要

个体在阿尔茨海默病谱中对 Tau 病理学的弹性机制尚不清楚。需要进行纵向研究,以揭示哪些因素与认知(即认知弹性)和大脑结构(即大脑弹性)相关,尽管 Tau 病理学大量存在,并阐明这些关联是横断面还是纵向的。我们使用纵向研究设计,通过正电子发射断层扫描(PET)来研究几种人口统计学、生物学和脑结构因素在产生对 Tau 病理学的认知和脑弹性方面的作用。在这项多中心研究中,我们纳入了 366 名基线时患有轻度认知障碍或阿尔茨海默病痴呆且有 18F-flortaucipir-PET 和纵向认知评估的淀粉样蛋白-β阳性个体。一个亚组(n=200)还接受了纵向结构磁共振成像。我们使用线性混合效应模型,以总体认知和皮质厚度为因变量,分别研究认知弹性和脑弹性的决定因素。模型评估了年龄、性别、受教育年限、APOE-ε4 状态、颅内体积(对于认知弹性模型为皮质厚度)是否改变了 Tau 病理学与认知下降或皮质变薄之间的关联。我们发现,较高的基线 Tau-PET 水平(在一个时间性的感兴趣区元内进行量化)与认知下降的速度(通过重复进行 Mini-Mental State Examination 进行测量)之间的关联受到年龄较大(Stβ相互作用=-0.062,P=0.032)、受教育程度较高(Stβ相互作用=-0.072,P=0.011)和颅内体积较大(Stβ相互作用=-0.07,P=0.016)的负面影响。年龄较小、受教育程度较高和皮质厚度较大与基线时更好的认知表现相关。皮质厚度较大与 Tau 负担独立相关,与认知下降速度较慢有关。较高的教育水平还改变了 Tau-PET 对皮质变薄的负面影响,而年龄较大与基线时较高的皮质厚度和较慢的皮质变薄速度相关,与 Tau 无关。我们的分析没有发现性别和 APOE-ε4 状态对认知和皮质厚度的(横断面或纵向)关联。在这项对有潜在阿尔茨海默病神经病理学变化的临床受损个体的纵向研究中,我们确定了教育是对 Tau 病理学的认知和大脑弹性的最有力决定因素。在认知下降方面,与 Tau 负担的观察到的相互作用表明,在 Tau 病理学水平较低时,教育可能具有保护认知下降和脑萎缩的作用,随着病理的进展,可能会耗尽弹性资源。最后,我们没有发现性别对大脑或认知弹性的主要贡献,这表明以前性别与弹性之间的联系可能主要是由横断面差异驱动的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e655/10473572/ce8a6e1b5dbc/awad100f1.jpg

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