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散发性路易体病和帕金森病中黑质神经元丢失的分期依赖性

Stage-dependent nigral neuronal loss in incidental Lewy body and Parkinson's disease.

作者信息

Dijkstra Anke A, Voorn Pieter, Berendse Henk W, Groenewegen Henk J, Rozemuller Annemieke J M, van de Berg Wilma D J

机构信息

Department of Anatomy and Neurosciences, section of Functional Neuroanatomy, VU University Medical Center, Amsterdam, the Netherlands.

出版信息

Mov Disord. 2014 Sep;29(10):1244-51. doi: 10.1002/mds.25952. Epub 2014 Jul 3.

Abstract

To gain a better understanding of the significance of α-synuclein pathological conditions during disease progression in Parkinson's disease, we investigated whether 1) nigral neuronal loss in incidental Lewy body disease and Parkinson's disease donors is associated with the local burden α-synuclein pathological conditions during progression of pathological conditions; 2) the burden and distribution of α-synuclein pathological conditions are related to clinical measures of disease progression. Post-mortem tissue and medical records of 24 Parkinson's disease patients, 20 incidental Lewy body disease donors, and 12 age-matched controls were obtained from the Netherlands Brain Bank for morphometric analysis. We observed a 20% decrease in nigral neuronal cell density in incidental Lewy body disease compared with controls. Nigral neuronal loss (12%) was already observed before the appearance α-synuclein aggregates. The progression from Braak α-synuclein stage 3 to 4 was associated with a significant decline in neuronal cell density (46%). Nigral neuronal loss increased with later Braak α-synuclein stages but did not vary across consecutive Braak α-synuclein stages. We observed a negative correlation between neuronal density and local α-synuclein burden in the substantia nigra of Parkinson's disease patients (ρ = -0.54), but no relationship with Hoehn & Yahr stage or disease duration. In conclusion, our findings cast doubt on the pathogenic role of α-synuclein aggregates in elderly, but do suggest that the severity of neurodegeneration and local burden of α-synuclein pathological conditions are closely coupled during disease progression in Parkinson's disease.

摘要

为了更好地理解帕金森病疾病进展过程中α-突触核蛋白病理状态的意义,我们研究了:1)偶发性路易体病和帕金森病供体中黑质神经元丢失是否与病理状态进展过程中局部α-突触核蛋白病理状态的负担相关;2)α-突触核蛋白病理状态的负担和分布是否与疾病进展的临床指标相关。从荷兰脑库获取了24例帕金森病患者、20例偶发性路易体病供体和12例年龄匹配的对照的尸检组织及医疗记录,进行形态计量分析。我们观察到,与对照组相比,偶发性路易体病中黑质神经元细胞密度降低了20%。在α-突触核蛋白聚集体出现之前就已观察到黑质神经元丢失(12%)。从Braak α-突触核蛋白3期进展到4期与神经元细胞密度显著下降(46%)相关。黑质神经元丢失随着Braak α-突触核蛋白后期阶段增加,但在连续的Braak α-突触核蛋白阶段之间没有差异。我们观察到帕金森病患者黑质中神经元密度与局部α-突触核蛋白负担之间呈负相关(ρ = -0.54),但与Hoehn & Yahr分期或病程无关。总之,我们的研究结果对α-突触核蛋白聚集体在老年人中的致病作用提出了质疑,但确实表明在帕金森病疾病进展过程中,神经退行性变的严重程度与α-突触核蛋白病理状态的局部负担密切相关。

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