Emdina Anna, Hermann Peter, Varges Daniela, Nuhn Sabine, Goebel Stefan, Bunck Timothy, Maass Fabian, Schmitz Matthias, Llorens Franc, Kruse Niels, Lingor Paul, Mollenhauer Brit, Zerr Inga
Department of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Bellvitge Biomedical Research Institute (IDIBELL), Hospitalet de Llobregat, 08908 Barcelona, Spain.
Diagnostics (Basel). 2022 May 18;12(5):1259. doi: 10.3390/diagnostics12051259.
Biomarkers are increasingly recognized as tools in the diagnosis and prognosis of neurodegenerative diseases. No fluid biomarker for Parkinson’s disease (PD) has been established to date, but α-synuclein, a major component of Lewy bodies in PD and dementia with Lewy bodies (DLB), has become a promising candidate. Here, we investigated CSF α-synuclein in patients with PD (n = 28), PDD (n = 8), and DLB (n = 5), applying an electrochemiluminescence immunoassay. Median values were non-significantly (p = 0.430) higher in patients with PDD and DLB (287 pg/mL) than in PD (236 pg/mL). A group of n = 36 primarily non-demented patients with PD and PDD was clinically followed for up to two years. A higher baseline α-synuclein was associated with increases in Hoehn and Yahr classifications (p = 0.019) and Beck Depression Inventory scores (p < 0.001) as well as worse performance in Trail Making Test A (p = 0.017), Trail Making Test B (p = 0.043), and the Boston Naming Test (p = 0.002) at follow-up. Surprisingly, higher levels were associated with a better performance in semantic verbal fluency tests (p = 0.046). In summary, CSF α-synuclein may be a potential prognostic marker for disease progression, affective symptoms, and executive cognitive function in PD. Larger-scaled studies have to validate these findings and the discordant results for single cognitive tests in this exploratory investigation.
生物标志物越来越被视为神经退行性疾病诊断和预后的工具。迄今为止,尚未建立帕金森病(PD)的体液生物标志物,但α-突触核蛋白是PD和路易体痴呆(DLB)中路易小体的主要成分,已成为一个有前景的候选标志物。在此,我们应用电化学发光免疫分析法,对28例PD患者、8例帕金森病痴呆(PDD)患者和5例DLB患者的脑脊液α-突触核蛋白进行了研究。PDD和DLB患者的中位数(287 pg/mL)略高于PD患者(236 pg/mL),但差异无统计学意义(p = 0.430)。一组共36例主要为非痴呆的PD和PDD患者接受了长达两年的临床随访。较高的基线α-突触核蛋白与随访时Hoehn和Yahr分级增加(p = 0.019)、贝克抑郁量表评分升高(p < 0.001)以及连线测验A(p = 0.017)、连线测验B(p = 0.043)和波士顿命名测验(p = 0.002)表现较差相关。令人惊讶的是,较高水平与语义言语流畅性测试中较好的表现相关(p = 0.046)。总之,脑脊液α-突触核蛋白可能是PD疾病进展、情感症状和执行认知功能的潜在预后标志物。更大规模的研究必须验证这些发现以及本次探索性研究中单一认知测试的不一致结果。