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多系统萎缩和帕金森病患者小脑的病理变化——一项立体学研究。

Pathological changes in the cerebellum of patients with multiple system atrophy and Parkinson's disease-a stereological study.

机构信息

Research Laboratory for Stereology and Neuroscience, Department of Neurology, Bispebjerg-Frederiksberg Hospital, Nielsine Nielsens Vej 6B, DK-2400, Copenhagen, Denmark.

Institute of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3, DK-2200, Copenhagen, Denmark.

出版信息

Brain Pathol. 2020 May;30(3):576-588. doi: 10.1111/bpa.12806. Epub 2020 Jan 6.

Abstract

Multiple system atrophy (MSA) and Parkinson's disease (PD) are synucleinopathies characterized by aggregation of α-synuclein in brain cells. Recent studies have shown that morphological changes in terms of cerebral nerve cell loss and increase in glia cell numbers, the degree of brain atrophy and molecular and epidemiological findings are more severe in MSA than PD. In the present study, we performed a stereological comparison of cerebellar volumes, granule and Purkinje cells in 13 patients diagnosed with MSA [8 MSA-P (striatonigral subtype) and 5 MSA-C (olivopontocerebellar subtype)], 12 PD patients, and 15 age-matched control subjects. Only brains from MSA-C patients showed a reduction in the total number of Purkinje cells (anterior lobe) whereas both MSA-P and MSA-C patients had reduced Purkinje cell volumes (perikaryons and nuclei volume). The cerebellum of both diseases showed a reduction in the white matter volume compared to controls. The number of granule cells was unaffected in both diseases. Analyses of cell type-specific mRNA expression supported our structural data. This study of the cerebellum is in line with previous findings in the cerebrum and demonstrates that the degree of morphological changes is more pronounced in MSA-C than MSA-P and PD. Further, our results support an explicit involvement of cerebellar Purkinje cells and white matter connectivity in MSA-C > MSA-P and points to the potential importance of white matter alterations in PD pathology.

摘要

多系统萎缩(MSA)和帕金森病(PD)是两种以α-突触核蛋白在脑细胞中聚集为特征的突触核蛋白病。最近的研究表明,MSA 的神经细胞丢失和神经胶质细胞数量增加、脑萎缩程度以及分子和流行病学发现等形态学变化比 PD 更为严重。在本研究中,我们对 13 名被诊断为 MSA 的患者[8 名 MSA-P(纹状体黑质亚型)和 5 名 MSA-C(橄榄脑桥小脑萎缩亚型)]、12 名 PD 患者和 15 名年龄匹配的对照组患者的小脑体积、颗粒细胞和浦肯野细胞进行了立体学比较。只有 MSA-C 患者的浦肯野细胞总数减少(前叶),而 MSA-P 和 MSA-C 患者的浦肯野细胞体积(胞体和核体积)减少。与对照组相比,两种疾病的小脑白质体积均减少。两种疾病的颗粒细胞数量均未受影响。细胞类型特异性 mRNA 表达分析支持我们的结构数据。这项对小脑的研究与大脑的先前发现一致,表明 MSA-C 的形态学变化程度比 MSA-P 和 PD 更为明显。此外,我们的结果支持小脑浦肯野细胞和白质连接在 MSA-C 中的明确参与,以及在 PD 病理中白质改变的潜在重要性。

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