Sheng Ze-Hu, Ma Ling-Zhi, Liu Jia-Yao, Ou Ya-Nan, Zhao Bing, Ma Ya-Hui, Tan Lan
Department of Neurology, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
Front Aging Neurosci. 2022 Dec 16;14:1061096. doi: 10.3389/fnagi.2022.1061096. eCollection 2022.
Neurofilament light chain protein (NfL) in cerebrospinal fluid (CSF) reflects the severity of neurodegeneration, with its altered concentrations discovered in Parkinson's disease (PD) and Parkinson's disease dementia (PD-D).
To determine whether CSF NfL, a promising biomarker of neuronal/axonal damage, can be used to monitor cognitive progression in Parkinson's disease and predict future cognitive decline.
A total of 259 people were recruited in this study, including 85 healthy controls (HC) and 174 neonatal PD patients from the Parkinson's Progression Markers Initiative (PPMI). Multiple linear regression and linear mixed effects models were used to examine the associations of baseline/longitudinal CSF NfL with cognitive decline and other CSF biomarkers. Kaplan-Meier analysis and log-rank test were used to compare the cumulative probability risk of cognition progression during the follow-up. Multivariate cox regression was used to detect cognitive progression in PD.
We found PD patients with mild cognitive impairment (PD-MCI) was higher than with normal cognition (PD-NC) in terms of CSF NfL baseline levels ( = 0.003) and longitudinal increase rate ( = 0.034). Both baseline CSF NfL and its rate of change predicted measurable cognitive decline in PD (MoCA, = -0.010, = 0.011; = -0.0002, < 0.001, respectively). The predictive effects in PD patients aged >65, male, ill-educated (<13 years) and without carrying Apolipoprotein E () seemed to be more obvious and reflected in more domains investigated. We also observed that CSF NfL levels predicted progression in PD patients with different cognitive diagnosis and amyloid status. After an average follow-up of 6.66 ± 2.54 years, higher concentration above the median of baseline CSF NfL was associated with a future high risk of PD with dementia (adjusted HR 2.82, 95% CI: 1.11-7.20, = 0.030).
Our results indicated that CSF NfL is a promising prognostic predictor of PD, and its concentration and dynamics can monitor the severity and progression of cognitive decline in PD patients.
脑脊液(CSF)中的神经丝轻链蛋白(NfL)反映神经退行性变的严重程度,帕金森病(PD)和帕金森病痴呆(PD-D)患者脑脊液中NfL浓度发生改变。
确定脑脊液NfL这一有前景的神经元/轴突损伤生物标志物是否可用于监测帕金森病患者的认知进展并预测未来认知功能下降。
本研究共纳入259人,包括85名健康对照(HC)和来自帕金森病进展标志物倡议(PPMI)的174例帕金森病患者。采用多元线性回归和线性混合效应模型来研究基线/纵向脑脊液NfL与认知功能下降及其他脑脊液生物标志物之间的关联。采用Kaplan-Meier分析和对数秩检验比较随访期间认知进展的累积概率风险。采用多因素Cox回归检测帕金森病患者的认知进展情况。
我们发现,帕金森病伴轻度认知障碍(PD-MCI)患者脑脊液NfL基线水平(P = 0.003)和纵向升高率(P = 0.034)均高于认知正常的帕金森病(PD-NC)患者。脑脊液NfL基线水平及其变化率均能预测帕金森病患者可测量的认知功能下降(蒙特利尔认知评估量表,P = -0.010,P = 0.011;P = -0.0002,P < 0.001)。在年龄>65岁、男性、受教育程度低(<13年)且未携带载脂蛋白E(ApoE)的帕金森病患者中,其预测作用似乎更明显,且体现在更多研究领域。我们还观察到,脑脊液NfL水平可预测不同认知诊断和淀粉样蛋白状态的帕金森病患者的病情进展。平均随访6.66±2.54年后,基线脑脊液NfL浓度高于中位数与未来患帕金森病痴呆的高风险相关(校正风险比2.82,95%置信区间:1.11 - 7.20,P = 0.030)。
我们的结果表明,脑脊液NfL是帕金森病有前景的预后预测指标,其浓度和动态变化可监测帕金森病患者认知功能下降的严重程度和进展情况。