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帕金森病患者对α-突触核蛋白种子扩增检测生物标志物在帕金森病诊断中作用的看法。

A perspective of persons with Parkinson's disease on the contribution of alpha-synuclein seed amplification assay biomarker to the diagnosis of Parkinson's disease.

作者信息

Bowen Susanne, Blacker David, Prettyman Richard

机构信息

Independent Researcher, Westfield, IN, USA.

Perron Institute for Neurological and Translational Science, Nedlands, Western Australia. University of Western Australia, Nedlands, Western Australia, Australia.

出版信息

J Parkinsons Dis. 2025 Aug;15(5):953-956. doi: 10.1177/1877718X251315651. Epub 2025 Feb 6.

Abstract

Alpha-synuclein is a normal protein, but misfolded forms in the cerebrospinal fluid can be detected using the alpha-synuclein seed amplification assay (αSyn-SAA), a potential biomarker for Parkinson's disease (PD). Some experts consider this assay a 'game changer' for redefining and reclassifying PD. In this article, we, three individuals with PD, share our perspective on the suitability of αSyn-SAA as the basis for a new classification and staging system for PD. We also discuss other biomarkers and their relevance to those with PD, drawing on our research and the scientific background of two authors. We aim to clarify complex media reports and study findings for the PD community. We argue that while αSyn-SAA can identify the presence of pathology, it cannot explain the underlying cause for such pathology or predict the progression of PD. Given the varied biological pathways leading to PD, using αSyn-SAA as a unified biological definition for a new classification system is premature. Further research is needed before it can serve as the foundation for defining and staging Parkinson's disease. Although αSyn-SAA has its place, like the DAT scan, it should be seen as a tool for confirming diagnoses rather than defining them.

摘要

α-突触核蛋白是一种正常蛋白质,但脑脊液中错误折叠的形式可通过α-突触核蛋白种子扩增检测法(αSyn-SAA)检测到,这是帕金森病(PD)的一种潜在生物标志物。一些专家认为这种检测方法是重新定义和重新分类帕金森病的“变革者”。在本文中,我们三位帕金森病患者分享了我们对于αSyn-SAA作为帕金森病新分类和分期系统基础的适用性的看法。我们还借鉴我们的研究以及两位作者的科学背景,讨论了其他生物标志物及其与帕金森病患者的相关性。我们旨在为帕金森病群体澄清复杂的媒体报道和研究结果。我们认为,虽然αSyn-SAA可以识别病理状态的存在,但它无法解释这种病理状态的潜在原因,也无法预测帕金森病的进展。鉴于导致帕金森病的生物途径多种多样,将αSyn-SAA用作新分类系统的统一生物学定义还为时过早。在它能够作为定义和分期帕金森病的基础之前,还需要进一步的研究。尽管αSyn-SAA有其作用,就像多巴胺转运体(DAT)扫描一样,它应被视为一种辅助诊断的工具,而非用于定义疾病。

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