Lin Chin-Hsien, Yang Shieh-Yueh, Horng Herng-Er, Yang Che-Chuan, Chieh Jen-Jie, Chen Hsin-Hsien, Liu Bing-Hsien, Chiu Ming-Jang
Neurology, National Taiwan University Hospital, Taipei, Taiwan.
MagQu Co., Ltd., Taipei, Taiwan.
J Neurol Neurosurg Psychiatry. 2017 Oct;88(10):818-824. doi: 10.1136/jnnp-2016-314857. Epub 2017 May 26.
α-Synuclein is critical to the pathogenesis of Parkinson's disease (PD). Few studies examined the plasma levels of α-synuclein due to the exceptionally low level of α-synuclein in plasma compared with cerebrospinal fluid. We aimed to investigate plasma α-synuclein in patients with PD of different disease severity.
There were total 114 participants, including 80 patients with PD and 34 controls, in the study. Participants received a complete evaluation of motor and non-motor symptoms, including cognitive function. We applied immunomagnetic reduction-based immunoassay to measure plasma levels of α-synuclein.
Plasma levels of α-synuclein were significantly higher in patients with PD compared with controls (median: 1.56 pg/mL, 95% CI 1.02 to 1.98 pg/mL vs 0.02 pg/mL, 95% CI 0.01 to 0.03 pg/mL; p<0.0001). Although there was a significant increase in plasma α-synuclein levels in PD patients with a higher Hoehn-Yahr (H-Y) stage, there was no correlation with motor symptom severity, as assessed by Unified Parkinson's Disease Rating Scale part III scores, after confounders (age, gender, and disease duration) were taken into account. However, plasma α-synuclein levels were significantly higher in PD patients with dementia (PDD) than in PD patients with mild cognitive impairment (PD-MCI) or normal cognition (0.42 pg/mL, (95% CI 0.25 to 0.93) for PD with normal cognition; 1.29 pg/mL (95% CI 0.76 to 1.93) for PD-MCI and 4.09 pg/mL (95% CI 1.99 to 6.19) for PDD, p<0.01) and were negatively correlated with Mini-Mental State Examination scores (R-adjusted=0.3004, p<0.001), even after confounder adjustment.
Our data suggest that plasma α-synuclein level correlates with cognitive decline but not motor severity in patients with PD. Plasma α-synuclein could serve as a surrogate biomarker for patients at risk of cognitive decline.
α-突触核蛋白对帕金森病(PD)的发病机制至关重要。由于血浆中α-突触核蛋白水平与脑脊液相比极低,很少有研究检测血浆中α-突触核蛋白水平。我们旨在研究不同疾病严重程度的PD患者的血浆α-突触核蛋白水平。
本研究共有114名参与者,包括80名PD患者和34名对照。参与者接受了包括认知功能在内的运动和非运动症状的全面评估。我们应用基于免疫磁珠减少的免疫测定法来测量血浆中α-突触核蛋白水平。
与对照组相比,PD患者血浆中α-突触核蛋白水平显著更高(中位数:1.56 pg/mL,95%可信区间1.02至1.98 pg/mL,而对照组为0.02 pg/mL,95%可信区间0.01至0.03 pg/mL;p<0.0001)。虽然Hoehn-Yahr(H-Y)分期较高的PD患者血浆α-突触核蛋白水平显著升高,但在考虑混杂因素(年龄、性别和病程)后,与统一帕金森病评定量表第三部分评分评估的运动症状严重程度无相关性。然而,痴呆型PD(PDD)患者的血浆α-突触核蛋白水平显著高于轻度认知障碍型PD(PD-MCI)或认知正常的PD患者(认知正常的PD患者为0.42 pg/mL,(95%可信区间0.25至0.93);PD-MCI患者为1.29 pg/mL(95%可信区间0.76至1.93),PDD患者为4.09 pg/mL(95%可信区间1.99至6.19),p<0.01),并且即使在调整混杂因素后,与简易精神状态检查表评分呈负相关(调整后R=0.3004,p<0.001)。
我们的数据表明,PD患者血浆α-突触核蛋白水平与认知功能下降相关,但与运动严重程度无关。血浆α-突触核蛋白可作为认知功能下降风险患者的替代生物标志物。