Chen Jia-Hung, Chan Lung, Chung Chen-Chih, Bamodu Oluwaseun Adebayo, Hong Chien-Tai
Department of Neurology, Shuang Ho Hospital, Taipei Medical University, New Taipei City 235, Taiwan.
Department of Neurology, School of Medicine, College of Medicine, Taipei Medical University, Taipei City 110, Taiwan.
J Clin Med. 2021 Oct 29;10(21):5085. doi: 10.3390/jcm10215085.
Elevated blood neurofilament light chain (NfL), which indicates the loss of neuronal integrity, is increasingly implicated as a diagnostic and outcome-predicting biomarker for neurological diseases. However, its diagnostic implication for Parkinson's disease (PD) remains unclear, with conflicting data reported by several studies. This may result from the demographic heterogeneity of the studied cohorts. The present study investigated the comparability of blood NfL between a domestic, single-centered PD cohort from Shuang Ho Hospital (SHH) in Taiwan, with the large international, multi-center cohort, Parkinson's Progression Markers Initiative (PPMI). In the SHH PD cohort, with 61 people with PD (PwP) and 25 healthy non-PD controls, plasma NfL unexpectedly was significantly higher in the control group than PwP (14.42 ± 13.84 vs. 9.39 ± 6.91 pg/mL, = 0.05). Interestingly, subgroup analysis revealed a non-significant difference of plasma NfL levels in male PwP compared with controls (8.58 ± 6.21 vs. 7.25 ± 4.43 pg/mL, =0.575), whereas NfL levels were significantly lower in the female PwP group than in their healthy control peers (10.29 ± 7.62 vs. 17.79 ± 15.52 pg/mL, = 0.033). Comparative analysis of the SHH and PPMI cohorts revealed a comparable gender-stratified distribution of blood NfL based on approximate theoretical quantiles. After adjusting for age and gender, no apparent difference in NfL value distribution was observed between the SHH and PPMI cohorts' control or PD groups. Significant downregulation of blood NfL levels were positively correlated with a reduced probability of having a PD diagnosis in both cohorts. These results demonstrated that the adjustment for demographic background enhances comparability between cohorts, and may be required to eliminate covariate/confounder-associated conflict in blood NfL results between different PD studies. This experience may be beneficial to other researchers around the world who are saddled with limited study participants, especially as data from small cohort sizes are often at greater risk of being skewed by specific variables.
血液神经丝轻链(NfL)水平升高表明神经元完整性受损,越来越多地被认为是神经系统疾病的诊断和预后预测生物标志物。然而,其对帕金森病(PD)的诊断意义仍不明确,多项研究报告的数据相互矛盾。这可能是由于研究队列的人口统计学异质性所致。本研究调查了台湾双和医院(SHH)的一个国内单中心PD队列与大型国际多中心队列帕金森病进展标志物倡议(PPMI)之间血液NfL的可比性。在SHH的PD队列中,有61例帕金森病患者(PwP)和25名健康非PD对照者,血浆NfL出人意料地在对照组中显著高于PwP(14.42±13.84 vs. 9.39±6.91 pg/mL,P = 0.05)。有趣的是,亚组分析显示男性PwP的血浆NfL水平与对照组相比无显著差异(8.58±6.21 vs. 7.25±4.43 pg/mL,P = 0.575),而女性PwP组的NfL水平显著低于其健康对照者(10.29±7.62 vs. 17.79±15.52 pg/mL,P = 0.033)。SHH和PPMI队列的比较分析显示,基于近似理论分位数,血液NfL的性别分层分布具有可比性。在调整年龄和性别后,SHH和PPMI队列的对照组或PD组之间未观察到NfL值分布的明显差异。血液NfL水平的显著下调与两个队列中PD诊断概率的降低呈正相关。这些结果表明,对人口统计学背景进行调整可提高队列之间的可比性,可能需要消除不同PD研究之间血液NfL结果中协变量/混杂因素相关的冲突。这种经验可能对世界各地研究参与者有限的其他研究人员有益,特别是因为小队列规模的数据往往更容易受到特定变量的影响而产生偏差。