Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, INSERM, CNRS, 75013 Paris, France.
ICM, Centre de NeuroImagerie de Recherche - CENIR, 75013 Paris, France.
Brain. 2021 Nov 29;144(10):3114-3125. doi: 10.1093/brain/awab191.
In Parkinson's disease, there is a progressive reduction in striatal dopaminergic function, and loss of neuromelanin-containing dopaminergic neurons and increased iron deposition in the substantia nigra. We tested the hypothesis of a relationship between impairment of the dopaminergic system and changes in the iron metabolism. Based on imaging data of patients with prodromal and early clinical Parkinson's disease, we assessed the spatiotemporal ordering of such changes and relationships in the sensorimotor, associative and limbic territories of the nigrostriatal system. Patients with Parkinson's disease (disease duration < 4 years) or idiopathic REM sleep behaviour disorder (a prodromal form of Parkinson's disease) and healthy controls underwent longitudinal examination (baseline and 2-year follow-up). Neuromelanin and iron sensitive MRI and dopamine transporter single-photon emission tomography were performed to assess nigrostriatal levels of neuromelanin, iron, and dopamine. For all three functional territories of the nigrostriatal system, in the clinically most and least affected hemispheres separately, the following was performed: cross-sectional and longitudinal intergroup difference analysis of striatal dopamine and iron, and nigral neuromelanin and iron; in Parkinson's disease patients, exponential fitting analysis to assess the duration of the prodromal phase and the temporal ordering of changes in dopamine, neuromelanin or iron relative to controls; and voxel-wise correlation analysis to investigate concomitant spatial changes in dopamine-iron, dopamine-neuromelanin and neuromelanin-iron in the substantia nigra pars compacta. The temporal ordering of dopaminergic changes followed the known spatial pattern of progression involving first the sensorimotor, then the associative and limbic striatal and nigral regions. Striatal dopaminergic denervation occurred first followed by abnormal iron metabolism and finally neuromelanin changes in the substantia nigra pars compacta, which followed the same spatial and temporal gradient observed in the striatum but shifted in time. In conclusion, dopaminergic striatal dysfunction and cell loss in the substantia nigra pars compacta are interrelated with increased nigral iron content.
在帕金森病中,纹状体多巴胺能功能逐渐降低,黑质中含神经黑色素的多巴胺能神经元丢失和铁沉积增加。我们检验了多巴胺能系统损伤与铁代谢变化之间存在相关性的假说。根据前驱期和早期临床帕金森病患者的影像学数据,我们评估了这种变化的时空顺序以及黑质纹状体系统感觉运动、联合和边缘区域中的关系。帕金森病患者(病程<4 年)或特发性 REM 睡眠行为障碍(帕金森病的前驱形式)和健康对照者接受了纵向检查(基线和 2 年随访)。进行了神经黑色素和铁敏感 MRI 和多巴胺转运体单光子发射断层扫描,以评估黑质纹状体的神经黑色素、铁和多巴胺水平。对于黑质纹状体系统的所有三个功能区域,分别在临床上最受影响和最不受影响的半球中,进行了以下分析:纹状体多巴胺和铁的横断面和纵向组间差异分析,以及黑质神经黑色素和铁的分析;在帕金森病患者中,进行指数拟合分析以评估前驱期的持续时间以及相对于对照组多巴胺、神经黑色素或铁变化的时间顺序;并进行体素相关性分析以研究黑质致密部多巴胺-铁、多巴胺-神经黑色素和神经黑色素-铁的同时空间变化。多巴胺能变化的时间顺序遵循已知的空间进展模式,首先涉及感觉运动,然后涉及联合和边缘纹状体和黑质区域。纹状体多巴胺能神经支配首先发生,然后是异常的铁代谢,最后是黑质致密部的神经黑色素变化,其遵循在纹状体中观察到的相同的时空梯度,但时间上有所转移。总之,纹状体内的多巴胺能功能障碍和黑质致密部的神经元丢失与黑质铁含量增加有关。