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路易体痴呆谱系中神经病理学特征的差异。

Differences in neuropathologic characteristics across the Lewy body dementia spectrum.

作者信息

Ballard C, Ziabreva I, Perry R, Larsen J P, O'Brien J, McKeith I, Perry E, Aarsland D

机构信息

Wolfson Centre for Age-Related Diseases, Wolfson Building, Guy's Campus, King's College London, London, SE1 1UL, UK.

出版信息

Neurology. 2006 Dec 12;67(11):1931-4. doi: 10.1212/01.wnl.0000249130.63615.cc.

Abstract

BACKGROUND

The objective of this comparative neuropathologic study was to determine the extent to which dementia with Lewy bodies (DLB) and Parkinson disease dementia (PDD) are distinct entities or part of a continuum with respect to the duration of parkinsonism.

METHODS

We evaluated the relationship between cortical alpha-synuclein pathology, plaques (Consortium to Establish a Registry for Alzheimer's Disease [CERAD]), tangles (Braak staging), and cholinergic deficits (choline acetyltransferase in temporal cortex) in 57 prospectively assessed patients (29 DLB, 28 PDD), confirmed at autopsy. The PDD group was divided according to the median duration of parkinsonism prior to dementia.

RESULTS

There was an association between longer duration of parkinsonism prior to dementia and less severe cortical alpha-synuclein pathology (chi(2) 10.4, df 2, p = 0.006) and lower CERAD plaque scores (chi(2) 26.6, df 9, p = 0.002), but not Braak staging. These findings were confirmed in a further correlation analysis, which also identified an unexpected correlation between more pronounced cortical cholinergic deficits and longer duration of parkinsonism prior to dementia (R = -0.37, p = 0.04).

CONCLUSION

While there is a clear relationship between the duration of Parkinson disease prior to the onset of dementia and key neuropathologic and neurochemical characteristics, there is a gradation of these differences across the dementia with Lewy bodies/Parkinson disease dementia spectrum and the findings do not support an arbitrary cut-off between the two disorders.

摘要

背景

这项比较神经病理学研究的目的是确定路易体痴呆(DLB)和帕金森病痴呆(PDD)在帕金森病病程方面是不同的实体还是连续统一体的一部分。

方法

我们评估了57例经尸检确诊的前瞻性评估患者(29例DLB,28例PDD)的皮质α-突触核蛋白病理学、斑块(阿尔茨海默病注册协会[CERAD])、缠结(Braak分期)和胆碱能缺陷(颞叶皮质中的胆碱乙酰转移酶)之间的关系。PDD组根据痴呆前帕金森病的病程中位数进行划分。

结果

痴呆前帕金森病病程较长与皮质α-突触核蛋白病理学较轻(χ² 10.4,自由度2,p = 0.006)和CERAD斑块评分较低(χ² 26.6,自由度9,p = 0.002)相关,但与Braak分期无关。这些发现在进一步的相关性分析中得到证实,该分析还发现痴呆前帕金森病病程较长与更明显的皮质胆碱能缺陷之间存在意外的相关性(R = -0.37,p = 0.04)。

结论

虽然痴呆发作前帕金森病的病程与关键的神经病理学和神经化学特征之间存在明确的关系,但在路易体痴呆/帕金森病痴呆谱系中这些差异存在梯度变化,且研究结果不支持在这两种疾病之间进行任意划分。

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