Coutinho Artur M, Ghilardi Maria Gabriela, Campos Ana Carolina P, Etchebehere Elba, Fonoff Fernanda C, Cury Rubens G, Pagano Rosana L, Martinez Raquel C R, Fonoff Erich T
Division of Neuroscience, Hospital Sírio-Libanês, Sao Paulo 01308-060, SP, Brazil.
Laboratory of Nuclear Medicine (LIM 43), Department of Radiology and Oncology, Faculdade de Medicina (FMUSP), Universidade de Sao Paulo, Sao Paulo 05403-010, SP, Brazil.
Biomedicines. 2023 Jan 20;11(2):296. doi: 10.3390/biomedicines11020296.
Parkinson's disease (PD) is characterized by a progressive loss of nigrostriatal dopaminergic neurons with impaired motor and non-motor symptoms. It has been suggested that motor asymmetry could be caused due to an imbalance in dopamine levels, as visualized by dopamine transporter single emission computed tomography test (DAT-SPECT), which might be related to indirect measures of neurodegeneration, evaluated by the Montreal Cognitive Assessment (MOCA) and α-synuclein levels in the cerebrospinal fluid (CSF). Therefore, this study aimed to understand the correlation between disease laterality, DAT-SPECT, cognition, and α-synuclein levels in PD.
A total of 28 patients in the moderate-advanced stage of PD were subjected to neurological evaluation, TRODAT-1-SPECT/CT imaging, MOCA, and quantification of the levels of α-synuclein.
We found that α-synuclein in the CSF was correlated with global cognition (positive correlation, r = 0.3, = 0.05) and DAT-SPECT concentration in the putamen (positive correlation, r = 0.4, = 0.005), and striatum (positive correlation, r = 0.2, = 0.03), thus working as a neurodegenerative biomarker. No other correlations were found between DAT-SPECT, CSF α-synuclein, and cognition, thus suggesting that they may be lost with disease progression.
Our data highlight the importance of understanding the dysfunction of the dopaminergic system in the basal ganglia and its complex interactions in modulating cognition.
帕金森病(PD)的特征是黑质纹状体多巴胺能神经元进行性丧失,伴有运动和非运动症状受损。有人提出,运动不对称可能是由于多巴胺水平失衡所致,这在多巴胺转运体单光子发射计算机断层扫描检查(DAT-SPECT)中可见,而这可能与通过蒙特利尔认知评估(MOCA)评估的神经变性间接指标以及脑脊液(CSF)中的α-突触核蛋白水平有关。因此,本研究旨在了解PD患者疾病偏侧性、DAT-SPECT、认知和α-突触核蛋白水平之间的相关性。
对28例中晚期PD患者进行神经学评估、TRODAT-1-SPECT/CT成像、MOCA以及α-突触核蛋白水平定量分析。
我们发现脑脊液中的α-突触核蛋白与整体认知(正相关,r = 0.3,P = 0.05)以及壳核(正相关,r = 0.4,P = 0.005)和纹状体(正相关,r = 0.2,P = 0.03)中的DAT-SPECT浓度相关,因此可作为一种神经变性生物标志物。在DAT-SPECT、脑脊液α-突触核蛋白和认知之间未发现其他相关性,这表明它们可能会随着疾病进展而丧失。
我们的数据强调了了解基底神经节中多巴胺能系统功能障碍及其在调节认知中的复杂相互作用的重要性。