Institute of Clinical Neurobiology, Alberichgasse 5/13, 1150, Vienna, Austria.
J Neural Transm (Vienna). 2019 Apr;126(4):423-431. doi: 10.1007/s00702-018-1898-9. Epub 2018 Jun 25.
Braak et al. proposed that cases with Lewy pathology in the peripheral nervous sytem, spinal cord and brain stem are prodromal Parkinson's disease (PD), suggesting a hypothesized progression of PD pathology. However, the putative potential of peripheral α-synuclein to promote brain pathology has been questioned recently. The Braak staging is a matter of vigorous debate, since < 100% of cases with Lewy pathology fitting the proposed PD staging scheme; however, most studies assessing typical PD cases show that the vast majority (80-100%) fit the Braak staging scheme. Incidental Lewy body disease and PD can show Lewy pathology in substantia nigra or other brain areas without involvement of dorsal motor nucleus of the vagus nerve. The Braak staging system is valid for PD patients with young onset, long duration with motor symptoms, but not for others, e.g., late onset and rapid course PD. The validity of Braak staging and its relationship to various subtypes of PD warrants further studies.
布拉克等人提出,在周围神经系统、脊髓和脑干中存在路易体病理的病例是前驱帕金森病(PD),提示 PD 病理存在假设的进展。然而,最近有人质疑外周α-突触核蛋白是否具有促进大脑病理的潜在能力。布拉克分期存在激烈的争论,因为符合 PD 分期方案的路易体病理的病例不到 100%;然而,评估典型 PD 病例的大多数研究表明,绝大多数(80-100%)符合布拉克分期方案。偶然的路易体病和 PD 可以在没有迷走神经背核参与的情况下在黑质或其他脑区显示路易体病理。布拉克分期系统适用于发病年龄早、持续时间长、伴有运动症状的 PD 患者,但不适用于其他患者,例如发病晚、病程快的 PD 患者。布拉克分期的有效性及其与各种 PD 亚型的关系需要进一步研究。