散发性帕金森病症状前和症状性病例脑病理分期的关键评价

G M Halliday, K Del Tredici, H Braak
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引用次数: 104

摘要

临床帕金森病(PD)是一种明显受益于多巴胺替代疗法的综合征。布拉克等人提出了散发性帕金森病的分期方法,假设α -突触核蛋白的异常沉积表明了导致临床帕金森病的细胞内过程。这种模式在将具有相似细胞机制的患者聚集在一起并确定可能预示临床综合征的潜在事件顺序方面具有优点。确定了进行性病理分期:1)临床前(1-2期),2)早期(3-4期,35%为临床PD)和3)晚期(5-6期,86%为临床PD)。然而,在抽样时,临床前、早期和晚期病例的平均年龄应该逐渐增大,这一特征在队列分析中没有观察到。在这个队列中,与其他类型的病例相比,临床前病例会发展为极晚发性PD。虽然分期方案是一个有价值的概念,但需要进一步发展。
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Critical appraisal of brain pathology staging related to presymptomatic and symptomatic cases of sporadic Parkinson's disease.

Clinical Parkinson's disease (PD) is a well-characterised syndrome that benefits significantly from dopamine replacement therapies. A staging procedure for sporadic PD pathology was developed by Braak et al. assuming that the abnormal deposition of alpha-synuclein indicates the intracellular process responsible for clinical PD. This paradigm has merit in corralling patients with similar cellular mechanisms together and determining the potential sequence of events that may herald the clinical syndrome. Progressive pathological stages were identified--1) preclinical (stages 1-2), 2) early (stages 3-4, 35% with clinical PD) and 3) late (stages 5-6, 86% with clinical PD). However, preclinical versus early versus late-stage cases should on average be progressively older at the time of sampling, a feature not observed in the cohort analysed. In this cohort preclinical cases would have developed extremely late-onset PD compared with the other types of cases analysed. While the staging scheme is a valuable concept, further development is required.

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