Rajmohan Ravi, Wen April, Henchcliffe Claire
Department of Neurology, University of California, Irvine. Irvine, CA, USA.
Department of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
Expert Rev Neurother. 2025 Aug;25(8):951-958. doi: 10.1080/14737175.2025.2515068. Epub 2025 Jun 29.
Parkinson's disease (PD) is a common neurodegenerative disease leading to motor and non-motor disabilities. Broadly accessible fluid- or tissue-based biomarkers will complement neuroimaging and may allow earlier identification and more precise tracking.
The authors have reviewed the recent advances from original full-text English-language articles that were indexed in the PubMed database between June 2023 and June 2024. Articles were identified using the PubMed MESH terms 'Parkinson's Disease' AND 'biomarkers' that focused on using a fluid or tissue-based biomarker to distinguish participants with PD from healthy controls or other conditions. The most promising new biomarkers are those measuring α-synuclein from cerebrospinal fluid or skin biopsy. A significant limitation of these studies is their reliance on a clinical diagnosis of PD, mostly without neuropathological confirmation.
Mounting evidence supports the validity of CSF and skin biopsy-based detection of α-synuclein for the distinction of PD from healthy controls, although not yet from the spectrum of α-synucleinopathies nor from non-α-synuclein forms of parkinsonism. Nonetheless, the potential to detect individuals who will develop PD may revolutionize our ability to test potential preventive interventions before motor symptoms develop. Machine-learning approaches offer promising strategies for efficient identification and validation of novel biomarkers.
帕金森病(PD)是一种常见的神经退行性疾病,会导致运动和非运动功能障碍。广泛可用的基于体液或组织的生物标志物将补充神经影像学检查,并可能有助于更早地识别和更精确地跟踪病情。
作者回顾了2023年6月至2024年6月期间在PubMed数据库中索引的英文原创全文文章的最新进展。使用PubMed医学主题词“帕金森病”和“生物标志物”来识别文章,这些文章专注于使用基于体液或组织的生物标志物来区分帕金森病患者与健康对照或其他疾病。最有前景的新生物标志物是那些测量脑脊液或皮肤活检中的α-突触核蛋白的标志物。这些研究的一个重大局限是它们依赖于帕金森病的临床诊断,大多数情况下没有神经病理学确认。
越来越多的证据支持基于脑脊液和皮肤活检检测α-突触核蛋白以区分帕金森病患者与健康对照的有效性,尽管尚未能区分α-突触核蛋白病谱系或非α-突触核蛋白形式的帕金森综合征。尽管如此,检测出可能患帕金森病的个体的潜力可能会彻底改变我们在运动症状出现之前测试潜在预防干预措施的能力。机器学习方法为高效识别和验证新型生物标志物提供了有前景的策略。