Nerattini Matilde, Abenavoli Elisabetta Maria, Berti Valentina
Nuclear Medicine Unit, Department of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy.
Nuclear Medicine Unit, Azienda Ospedaliero-Universitaria Careggi, Florence, Italy.
Semin Nucl Med. 2025 Jul;55(4):565-576. doi: 10.1053/j.semnuclmed.2025.03.007. Epub 2025 May 4.
This review synthesizes recent literature, primarily from the last 5 years, to highlight the impact of innovative technologies and analytical approaches on the application of positron emission tomography (PET) in movement disorders. PET remains a cornerstone for investigating these conditions, with recent advancements enhancing our understanding of disease pathophysiology and progression. Established findings, such as the ability of [F]-fluorodeoxyglucose PET (18F-FDG PET) to differentiate Parkinson's disease (PD) from atypical parkinsonian syndromes based on characteristic metabolic patterns, have been consistently validated. PD typically presents with relative hypermetabolism in the basal ganglia, thalamus and cerebellum, while atypical parkinsonisms exhibit more widespread subcortical hypometabolism. Technological innovations, particularly in quantification methods and metabolic connectivity analysis, have improved diagnostic precision and provided deeper insights into disease mechanisms. Dopaminergic PET imaging, crucial for assessing presynaptic and postsynaptic dysfunction, has also benefited from these advances. The field is further evolving with the development of novel tracers targeting pathological hallmarks, such as alpha-synuclein in PD and multiple system atrophy (MSA), tau in progressive supranuclear palsy (PSP) and cortico-basal degeneration (CBD), and tracers for neuroinflammation, microglial activation, and neurotransmitter systems like serotonin and acetylcholine. While PET is not yet routinely used for the clinical assessment of Huntington's disease or ataxia, research applications are expanding, driven by the potential of these new tracers and analytical techniques. These advancements not only reinforce existing knowledge but also open new avenues for enhancing the understanding and management of movement disorders.
本综述综合了主要来自过去5年的近期文献,以突出创新技术和分析方法对正电子发射断层扫描(PET)在运动障碍应用中的影响。PET仍然是研究这些疾病的基石,最近的进展加深了我们对疾病病理生理学和进展的理解。既定的发现,如[F] - 氟脱氧葡萄糖PET(18F - FDG PET)基于特征性代谢模式区分帕金森病(PD)和非典型帕金森综合征的能力,已得到持续验证。PD通常表现为基底神经节、丘脑和小脑相对代谢亢进,而非典型帕金森综合征则表现为更广泛的皮质下代谢减退。技术创新,特别是在定量方法和代谢连接性分析方面,提高了诊断精度,并为疾病机制提供了更深入的见解。多巴胺能PET成像对于评估突触前和突触后功能障碍至关重要,也受益于这些进展。随着针对病理特征的新型示踪剂的开发,该领域正在进一步发展,例如针对PD和多系统萎缩(MSA)中的α-突触核蛋白、进行性核上性麻痹(PSP)和皮质基底节变性(CBD)中的tau以及神经炎症、小胶质细胞活化以及血清素和乙酰胆碱等神经递质系统的示踪剂。虽然PET尚未常规用于亨廷顿舞蹈病或共济失调的临床评估,但在这些新示踪剂和分析技术的推动下,研究应用正在不断扩大。这些进展不仅巩固了现有知识,还为加强对运动障碍的理解和管理开辟了新途径。