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

被引:72
|
作者
Polvikoski, T. M.
van Straaten, E. C. W. [2 ]
Barkhof, F. [3 ]
Sulkava, R. [4 ]
Aronen, H. J. [5 ]
Niinisto, L. [6 ]
Oinas, M. [7 ,8 ]
Scheltens, P. [2 ]
Erkinjuntti, T. [9 ]
Kalaria, R. N. [1 ]
机构
[1] Newcastle Univ, Wolfson Res Ctr Neuropathol, Inst Ageing & Hlth, Newcastle Upon Tyne NE4 5PL, Tyne & Wear, England
[2] Vrije Univ Amsterdam Med Ctr, Dept Neurol, Amsterdam, Netherlands
[3] Vrije Univ Amsterdam Med Ctr, Dept Radiol, Amsterdam, Netherlands
[4] Univ Kuopio, Dept Community Hlth & Gen Practice, FIN-70211 Kuopio, Finland
[5] Turku Univ, Cent Hosp, Dept Radiol, Turku, Finland
[6] Katriina Hosp, Vantaa, Finland
[7] Univ Helsinki, Dept Neurosurg, Helsinki, Finland
[8] Univ Helsinki, Dept Pathol, Helsinki, Finland
[9] Univ Helsinki, Dept Neurol, Helsinki, Finland
基金
英国医学研究理事会; 芬兰科学院; 美国国家卫生研究院;
关键词
ALZHEIMERS-DISEASE; VASCULAR DEMENTIA; LEWY BODIES; LESIONS; ATROPHY; RISK; POPULATION; CONSORTIUM; DEPOSITION; BRAIN;
D O I
10.1212/WNL.0b013e318200d6f9
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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. Neurology (R) 2010;75:2071-2078
引用
收藏
页码:2071 / 2078
页数:8
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