Berman Sara E, Siderowf Andrew D
Parkinson's Disease and Movement Disorders Center, Department of Neurology, Pennsylvania Hospital, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Cells. 2025 Aug 18;14(16):1272. doi: 10.3390/cells14161272.
Synucleinopathies are neurodegenerative disorders defined by the pathological aggregation of α-synuclein. Several α-synuclein biomarkers have been developed to aid diagnosis and research, such as cerebrospinal fluid (CSF) and blood-based measurements, seed amplification assays (SAAs), and immunohistochemical detection from skin biopsies. While these existing biomarkers have important uses, they face limitations in diagnostic specificity, spatial localization, and the ability to monitor disease progression or response to therapy. The development of α-synuclein PET tracers, which would allow for the direct in vivo imaging of α-synuclein, represents an important unmet need in both research and the clinical care of patients with movement disorders. This review outlines the current landscape of α-synuclein biomarkers and discusses both the scientific and technical challenges in developing α-synuclein PET imaging tracers.
突触核蛋白病是由α-突触核蛋白的病理性聚集所定义的神经退行性疾病。已经开发了几种α-突触核蛋白生物标志物来辅助诊断和研究,例如脑脊液(CSF)和基于血液的检测、种子扩增分析(SAA)以及皮肤活检的免疫组织化学检测。虽然这些现有的生物标志物有重要用途,但它们在诊断特异性、空间定位以及监测疾病进展或对治疗反应的能力方面面临局限性。α-突触核蛋白PET示踪剂的开发能够实现α-突触核蛋白的直接体内成像,这在运动障碍患者的研究和临床护理中都是一项尚未满足的重要需求。本综述概述了α-突触核蛋白生物标志物的当前情况,并讨论了开发α-突触核蛋白PET成像示踪剂所面临的科学和技术挑战。