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血管病理学对处于中间 Braak 阶段 tau 病理学的老年个体认知障碍的贡献。

The Contribution of Vascular Pathology Toward Cognitive Impairment in Older Individuals with Intermediate Braak Stage Tau Pathology.

机构信息

Division of Neuroscience & Experimental Psychology, Faculty of Biology, Medicine and Health, School of Biological Sciences, The University of Manchester, Salford Royal Hospital, Salford, UK.

Manchester Academic Health Science Centre (MAHSC), Manchester, UK.

出版信息

J Alzheimers Dis. 2020;77(3):1005-1015. doi: 10.3233/JAD-200339.

DOI:10.3233/JAD-200339
PMID:32804131
Abstract

BACKGROUND

The pathological features of Alzheimer's disease (AD) are well described but little is known as to how both neurodegeneration and vascular changes might interact in causing cognitive impairment.

OBJECTIVE

The present study aims to investigate relationships between vascular and AD pathology in cognitively healthy and cognitively impaired individuals with a particular emphasis on those at intermediate Braak tau stages.

METHODS

We investigated the interplay between Braak tau stage and measures of vascular pathology as described by the vascular cognitive impairment neuropathology guidelines (VCING) in 185 brains from the Brains for Dementia Research programme and The University of Manchester Longitudinal Study of Cognition in Healthy Old Age. VCING asserts that at least one large (>10 mm) infarct, moderate/severe occipital leptomeningeal cerebral amyloid angiopathy, and moderate/severe arteriosclerosis in occipital white matter accurately predicts the contribution of cerebrovascular pathology to cognitive impairment.

RESULTS

We found that the extent of arteriosclerosis in the occipital white matter did not differ between cognitive groups at intermediate (III-IV) Braak stages whereas moderate/severe leptomeningeal occipital cerebral amyloid angiopathy was greater in cognitively impaired than normal individuals at Braak stage III-IV. This finding remained significant after controlling for effects of age, sex, CERAD score, Thal phase, presence/severity of primary age-related tauopathy, presence/severity of limbic-predominant age-related TDP43 encephalopathy and small vessel disease in basal ganglia.

CONCLUSION

Interventions targeting cerebral amyloid angiopathy may contribute to delay the onset of cognitive impairment in individuals with intermediate Alzheimer's type pathology.

摘要

背景

阿尔茨海默病(AD)的病理特征已有详细描述,但对于神经退行性变和血管变化如何相互作用导致认知障碍知之甚少。

目的

本研究旨在探讨认知正常和认知障碍个体中血管和 AD 病理学之间的关系,特别关注处于中间 Braak tau 阶段的个体。

方法

我们研究了 Braak tau 阶段与血管认知障碍神经病理学指南(VCING)所描述的血管病理学测量之间的相互作用,该研究纳入了 185 例来自 Brains for Dementia Research 计划和曼彻斯特大学健康老年人群认知纵向研究的大脑。VCING 认为,至少一个大(>10mm)梗死、中度/重度枕叶脑皮质下脑淀粉样血管病和中度/重度枕叶脑白质动脉硬化准确预测了脑血管病理学对认知障碍的贡献。

结果

我们发现,在中间(III-IV)Braak 阶段,认知组之间的枕叶白质动脉硬化程度没有差异,而在认知障碍组中,III-IV 期的中度/重度枕叶脑皮质下脑淀粉样血管病比认知正常组更为严重。在控制年龄、性别、CERAD 评分、Thal 阶段、原发性年龄相关性 tau 病的存在/严重程度、边缘优势性年龄相关性 TDP43 脑病和基底节小血管疾病的影响后,这一发现仍然具有统计学意义。

结论

针对脑淀粉样血管病的干预措施可能有助于延缓具有中间阿尔茨海默病型病理学的个体认知障碍的发生。

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