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White matter lesions are associated with progression of medial temporal lobe atrophy in Alzheimer disease.白质病变与阿尔茨海默病中颞叶内侧萎缩的进展相关。
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老年人群额部脑白质高信号与神经纤维缠结病理

Frontal lobe white matter hyperintensities and neurofibrillary pathology in the oldest old.

机构信息

Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne, UK.

出版信息

Neurology. 2010 Dec 7;75(23):2071-8. doi: 10.1212/WNL.0b013e318200d6f9. Epub 2010 Nov 3.

DOI:10.1212/WNL.0b013e318200d6f9
PMID:21048201
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2995533/
Abstract

BACKGROUND

Current studies suggest an interaction between vascular mechanisms and neurodegenerative processes that leads to late-onset Alzheimer disease (AD). We tested whether AD pathology was associated with white matter hyperintensities (WMH) or cerebral infarcts in the oldest old individuals.

METHODS

Brains from 132 subjects over 85 years old, who came to autopsy from the Vantaa 85+ population-based cohort, were scanned by postmortem MRI and examined for neuropathologic changes. Coronal images were analyzed to determine the degree of frontal and parietal periventricular WMH (PVWMH) and deep WMH (DWMH) and cerebral infarcts. Neuropathologic variables included Consortium to Establish a Registry for Alzheimer's Disease scores for neuritic plaques and Braak staging among subjects in 5 groups: normal aging (NA), borderline with insufficient AD pathology, AD, AD plus other pathology, and other primary degenerative diseases.

RESULTS

Frontal DWMH were detected in >50% of the sample. Both frontal PVWMH and DWMH were significantly more extensive in the AD group compared to the NA group or the NA and borderline groups combined. Frontal PVWMH and DWMH were also associated with increased Braak staging (p = 0.03) and the neuritic plaque load (p = 0.01). Further analysis revealed there were a greater number of cerebral infarcts associated with frontal DWMH (p = 0.03) but not with frontal PVWMH.

CONCLUSIONS

Our study showed an association between neurofibrillary pathology and frontal PVWMH and DWMH (rather than parietal), as a surrogate of small vessel disease, particularly in very old community-dwelling individuals.

摘要

背景

目前的研究表明,血管机制与神经退行性过程之间存在相互作用,导致迟发性阿尔茨海默病(AD)。我们测试了 AD 病理学是否与最年长个体的白质高信号(WMH)或脑梗死有关。

方法

对来自万塔 85+人群为基础的队列中 132 名 85 岁以上接受尸检的个体的大脑进行死后 MRI 扫描,并检查神经病理学变化。对冠状图像进行分析,以确定额部和顶叶脑室周围 WMH(PVWMH)和深部 WMH(DWMH)以及脑梗死的程度。神经病理学变量包括 Consortium to Establish a Registry for Alzheimer's Disease 评分(用于评估神经纤维缠结和 Braak 分期),研究对象分为 5 组:正常老化(NA)、边界性 AD 病理学不足、AD、AD 合并其他病理学和其他原发性退行性疾病。

结果

50%的样本中检测到额部 DWMH。与 NA 组或 NA 和边界性组相比,AD 组的额部 PVWMH 和 DWMH 均明显更广泛。额部 PVWMH 和 DWMH 与 Braak 分期增加(p = 0.03)和神经纤维缠结负荷增加(p = 0.01)相关。进一步分析显示,与额部 DWMH 相关的脑梗死数量更多(p = 0.03),但与额部 PVWMH 无关。

结论

我们的研究表明,神经纤维病理学与额部 PVWMH 和 DWMH(而非顶叶)之间存在关联,作为小血管疾病的替代标志物,特别是在非常年长的社区居住者中。