Farotti Lucia, Paolini Paoletti Federico, Simoni Simone, Parnetti Lucilla
Section of Neurology, Department of Medicine, University of Perugia, Perugia, Italy.
Biomark Insights. 2020 Oct 12;15:1177271920964077. doi: 10.1177/1177271920964077. eCollection 2020.
Diagnosis of Parkinson's disease (PD) relies on clinical history and physical examination, but misdiagnosis is common in early stages. Identification of biomarkers for PD may allow for early and more precise diagnosis and provide information about prognosis. Developments in analytical chemistry allow for the detection of a large number of molecules in cerebrospinal fluid (CSF), which are known to be associated with the pathogenesis of PD. Given the pathophysiology of PD, CSF α-synuclein species have the strongest rationale for use, also providing encouraging preliminary results in terms of early diagnosis. In the field of classical Alzheimer's disease (AD) biomarkers, low CSF Aβ levels have shown a robust prognostic value in terms of development of cognitive impairment. Other CSF biomarkers including lysosomal enzymes, neurofilament light chain, markers of neuroinflammation and oxidative stress, although promising, have not proved to be reliable for diagnostic and prognostic purposes yet. Overall, the implementation of CSF biomarkers may give a substantial contribution to the optimal use of disease-modifying drugs.
帕金森病(PD)的诊断依赖于临床病史和体格检查,但在疾病早期误诊很常见。识别PD的生物标志物可能有助于早期更精确的诊断,并提供预后信息。分析化学的发展使得能够检测脑脊液(CSF)中大量已知与PD发病机制相关的分子。鉴于PD的病理生理学,脑脊液α-突触核蛋白种类最有理由被使用,在早期诊断方面也提供了令人鼓舞的初步结果。在经典阿尔茨海默病(AD)生物标志物领域,脑脊液Aβ水平低在认知障碍发展方面显示出强大的预后价值。其他脑脊液生物标志物,包括溶酶体酶、神经丝轻链、神经炎症和氧化应激标志物,尽管很有前景,但尚未被证明对诊断和预后目的可靠。总体而言,脑脊液生物标志物的应用可能会对疾病修饰药物的最佳使用做出重大贡献。