Bereczki Erika, Bogstedt Anna, Höglund Kina, Tsitsi Panagiota, Brodin Lovisa, Ballard Clive, Svenningsson Per, Aarsland Dag
Department of Neurobiology, Care Sciences and Society, Center for Alzheimer Research, Division for Neurogeriatrics, Karolinska Institutet, Novum, Stockholm Sweden.
Cardiovascular and Metabolic Diseases, Innovative Medicines and Early Development, AstraZeneca, Integrated Cardio Metabolic Centre (ICMC), Karolinska Institutet, Novum, Huddinge Sweden.
NPJ Parkinsons Dis. 2017 Feb 8;3:7. doi: 10.1038/s41531-017-0008-2. eCollection 2017.
Recent findings of morphological and functional changes in Parkinson's disease brains have shown altered synapse formation, but their role in cognitive decline is still an area under exploration. Here we measured the concentration of three key synaptic proteins, Rab3A, SNAP25 and neurogranin by enzyme-linked immunosorbent assay, in cerebrospinal fluid from a total of 139 participants (87 controls and 52 Parkinson's disease patients out of which 30 were drug-naïve) and explored their associations with motor and cognitive symptoms. Associations with motor disease stage (assessed by Hoehn and Yahr scale) and cognitive performance (assessed by the Montreal Cognitive Assessment scores) were explored. An overall increase in the concentration of SNAP25 was found in Parkinson's disease patients ( = 0.032). Increased neurogranin levels were found in the drug naïve patients subgroup ( = 0.023). Significant associations were observed between increased concentration of neurogranin and cognitive impairment in total Parkinson's disease group ( = 0.017), as well as in the drug naïve ( = 0.021) and with motor disease stage ( = 0.041). There were no significant disease-driven changes observed in the concentration of Rab3a. Concentrations SNAP25 and neurogranin were increased in cerebrospinal fluid of Parkinson's disease patients in a disease specific manner and related to cognitive and motor symptom severity. Future longitudinal studies should explore whether cerebrospinal fluid synaptic proteins can predict cognitive decline in Parkinson's disease.
帕金森病大脑形态和功能变化的最新研究结果显示突触形成发生改变,但其在认知衰退中的作用仍处于探索阶段。在此,我们通过酶联免疫吸附测定法测量了总共139名参与者(87名对照者和52名帕金森病患者,其中30名未接受药物治疗)脑脊液中三种关键突触蛋白Rab3A、SNAP25和神经颗粒素的浓度,并探讨了它们与运动和认知症状的关联。研究了与运动疾病阶段(通过霍恩和雅尔分级量表评估)和认知表现(通过蒙特利尔认知评估分数评估)的关联。发现帕金森病患者中SNAP25的浓度总体升高(P = 0.032)。在未接受药物治疗的患者亚组中发现神经颗粒素水平升高(P = 0.023)。在整个帕金森病组(P = 0.017)以及未接受药物治疗的患者中(P = 0.021),神经颗粒素浓度升高与认知障碍之间存在显著关联,并且与运动疾病阶段也存在显著关联(P = 0.041)。未观察到Rab3a浓度有明显的疾病驱动变化。帕金森病患者脑脊液中SNAP25和神经颗粒素的浓度以疾病特异性方式升高,且与认知和运动症状严重程度相关。未来的纵向研究应探讨脑脊液突触蛋白是否能够预测帕金森病的认知衰退。