Beach Thomas G, Adler Charles H, Lue LihFen, Sue Lucia I, Bachalakuri Jyothi, Henry-Watson Jonette, Sasse Jeanne, Boyer Sarah, Shirohi Scophil, Brooks Reed, Eschbacher Jennifer, White Charles L, Akiyama Haru, Caviness John, Shill Holly A, Connor Donald J, Sabbagh Marwan N, Walker Douglas G
Sun Health Research Institute, Sun City, AZ 85351, USA.
Acta Neuropathol. 2009 Jun;117(6):613-34. doi: 10.1007/s00401-009-0538-8. Epub 2009 Apr 28.
The two current major staging systems in use for Lewy body disorders fail to classify up to 50% of subjects. Both systems do not allow for large numbers of subjects who have Lewy-type alpha-synucleinopathy (LTS) confined to the olfactory bulb or who pass through a limbic-predominant pathway that at least initially bypasses the brainstem. The results of the current study, based on examination of a standard set of ten brain regions from 417 subjects stained immunohistochemically for alpha-synuclein, suggest a new staging system that, in this study, allows for the classification of all subjects with Lewy body disorders. The autopsied subjects included elderly subjects with Parkinson's disease, dementia with Lewy bodies, incidental Lewy body disease and Alzheimer's disease with Lewy bodies, as well as comparison groups without Lewy bodies. All subjects were classifiable into one of the following stages: I. Olfactory Bulb Only; IIa Brainstem Predominant; IIb Limbic Predominant; III Brainstem and Limbic; IV Neocortical. Progression of subjects through these stages was accompanied by a generally stepwise worsening in terms of striatal tyrosine hydroxylase concentration, substantia nigra pigmented neuron loss score, Mini Mental State Examination score and score on the Unified Parkinson's Disease Rating Scale Part 3. Additionally, there were significant correlations between these measures and LTS density scores. It is suggested that the proposed staging system would improve on its predecessors by allowing classification of a much greater proportion of cases.
目前用于路易体疾病的两种主要分期系统无法对多达50%的受试者进行分类。这两种系统都没有考虑到大量仅局限于嗅球的路易型α-突触核蛋白病(LTS)患者,或者那些至少在最初绕过脑干的以边缘系统为主的通路的患者。基于对417名受试者的一组标准的10个脑区进行免疫组织化学染色检测α-突触核蛋白的结果,本研究提出了一种新的分期系统,在本研究中,该系统能够对所有路易体疾病患者进行分类。尸检受试者包括患有帕金森病、路易体痴呆、偶然性路易体病和路易体合并阿尔茨海默病的老年受试者,以及无路易体的对照组。所有受试者均可分为以下阶段之一:I. 仅累及嗅球;IIa. 以脑干为主;IIb. 以边缘系统为主;III. 脑干和边缘系统;IV. 新皮质。受试者在这些阶段的进展伴随着纹状体酪氨酸羟化酶浓度、黑质色素神经元丢失评分、简易精神状态检查评分和统一帕金森病评定量表第3部分评分的普遍逐步恶化。此外,这些指标与LTS密度评分之间存在显著相关性。建议所提出的分期系统将通过对更大比例的病例进行分类而优于其前身。