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路易体痴呆症中脑淀粉样蛋白沉积的分布及其与临床表型的相关性。

Distribution of cerebral amyloid deposition and its relevance to clinical phenotype in Lewy body dementia.

机构信息

PET/CT Dementia Research Center, Juntendo Tokyo Koto Geriatric Medical Center, Juntendo University School of Medicine, Koto-ku, Tokyo 136-0075, Japan.

出版信息

Neurosci Lett. 2010 Dec 3;486(1):19-23. doi: 10.1016/j.neulet.2010.09.036. Epub 2010 Sep 17.

Abstract

Parkinson's disease dementia (PDD) and dementia with Lewy bodies (DLB) are clinically distinguished based only on the duration of parkinsonism prior to dementia. It is known that there is considerable pathological overlap between these two conditions, but the pathological difference between them remains unknown. We evaluated Alzheimer-type pathology in 30 brains of patients with Lewy body dementia using standardized methods based on those of the Brain-Net Europe (BNE) Consortium. Only 2 of 13 PDD cases (15%) showed Aβ-immunoreactive pathology in the midbrain (amyloid phase IV). In contrast, 12 of 17 DLB cases (71%) exhibited midbrain involvement. Four of the DLB cases (24%) but none of the PDD cases exhibited Aβ-immunoreactive pathology in the cerebellum (amyloid phase V). The ratio of cases with subtentorial involvement of amyloid deposition was significantly higher in DLB than in PDD. The median of amyloid phases was significantly greater in DLB than in PDD, but there was no difference in neurofibrillary tangle (NFT) Braak stages or in Lewy body scores. When patients were classified according to whether dementia or parkinsonism had occurred first, the rate of dementia having occurred first was significantly greater in amyloid phase IV and V than in phase 0-I, with phase III in the middle, though there was no significant difference in median NFT Braak stage or mean Lewy body score associated with amyloid phase. These results suggest that amyloid deposition may contribute to the timing of the onset of dementia relative to that of parkinsonism in Lewy body dementia.

摘要

帕金森病痴呆(PDD)和路易体痴呆(DLB)仅根据痴呆前帕金森病的持续时间进行临床区分。已知这两种疾病在病理学上有很大的重叠,但它们之间的病理学差异仍不清楚。我们使用基于欧洲脑网(BNE)联盟的标准化方法评估了 30 例路易体痴呆患者的阿尔茨海默病样病理学。只有 13 例 PDD 病例中的 2 例(15%)在中脑(淀粉样蛋白阶段 IV)显示出 Aβ 免疫反应性病理学。相比之下,17 例 DLB 病例中有 12 例(71%)表现出中脑受累。4 例 DLB 病例(24%)但无 1 例 PDD 病例在小脑(淀粉样蛋白阶段 V)中表现出 Aβ 免疫反应性病理学。DLB 中淀粉样沉积累及小脑的病例比例明显高于 PDD。DLB 的淀粉样蛋白分期中位数明显高于 PDD,但神经纤维缠结(NFT)Braak 分期或路易体评分无差异。当根据痴呆或帕金森病是否先发生对患者进行分类时,淀粉样蛋白阶段 IV 和 V 的痴呆先发生的比例明显高于阶段 0-I,而阶段 III 居中,尽管与淀粉样蛋白分期相关的 NFT Braak 分期中位数或平均路易体评分无显著差异。这些结果表明,在路易体痴呆中,淀粉样沉积可能与帕金森病相比,与痴呆的发病时间有关。

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