Department of Nuclear Medicine, University Medical Center, University of Leipzig, Leipzig, Germany;
Department of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania; and.
J Nucl Med. 2022 Jun;63(Suppl 1):68S-74S. doi: 10.2967/jnumed.121.263202.
The improvement of existing techniques and the development of new molecular imaging methods are an exciting and rapidly developing field in clinical care and research of neurodegenerative disorders. In the clinic, molecular imaging has the potential to improve early and differential diagnosis and to stratify and monitor therapy in these disorders. Meanwhile, in research, these techniques improve our understanding of the underlying pathophysiology and pathobiochemistry of these disorders and allow for drug testing. This article is an overview on our perspective on future developments in neurodegeneration tracers and the associated imaging technologies. For example, we predict that the current portfolio of β-amyloid and tau aggregate tracers will be improved and supplemented by tracers allowing imaging of other protein aggregation pathologies, such as α-synuclein and transactive response DNA binding protein 43 kDa. Future developments will likely also be observed in imaging neurotransmitter systems. This refers to both offering imaging to a broader population in cases involving the dopaminergic, cholinergic, and serotonergic systems and making possible the imaging of systems not yet explored, such as the glutamate and opioid systems. Tracers will be complemented by improved tracers of neuroinflammation and synaptic density. Technologywise, the use of hybrid PET/MRI, dedicated brain PET, and total-body PET scanners, as well as advanced image acquisition and processing protocols, will open doors toward broader and more efficient clinical use and novel research applications. Molecular imaging has the potential of becoming a standard and essential clinical and research tool to diagnose and study neurodegenerative disorders and to guide treatments. On that road, we will need to redefine the role of molecular imaging in relation to that of emerging blood-based biomarkers. Taken together, the unique features of molecular imaging-that is, the potential to provide direct noninvasive information on the presence, extent, localization, and quantity of molecular pathologic processes in the living body-together with the predicted novel tracer and imaging technology developments, provide optimism about a bright future for this approach to improved care and research on neurodegenerative disorders.
现有技术的改进和新的分子影像学方法的发展是临床神经退行性疾病诊疗和研究中令人兴奋且快速发展的领域。在临床实践中,分子影像学有可能改善早期和鉴别诊断,并对这些疾病进行分层和监测治疗。同时,在研究中,这些技术可以增进我们对这些疾病潜在病理生理学和病理生物化学的理解,并允许进行药物测试。本文概述了我们对神经退行性疾病示踪剂及其相关影像学技术未来发展的看法。例如,我们预计目前的β-淀粉样蛋白和 tau 聚集示踪剂组合将得到改进和补充,增加可用于成像其他蛋白聚集病理学的示踪剂,如 α-突触核蛋白和转导反应 DNA 结合蛋白 43 kDa。未来的发展也可能出现在神经递质系统的成像中。这既包括为涉及多巴胺能、胆碱能和 5-羟色胺能系统的病例中的更广泛人群提供成像,也包括使尚未探索的系统(如谷氨酸能和阿片能系统)的成像成为可能。示踪剂将得到神经炎症和突触密度的改进示踪剂的补充。在技术方面,使用混合正电子发射断层扫描/磁共振成像、专用脑正电子发射断层扫描、全身正电子发射断层扫描仪,以及先进的图像采集和处理协议,将为更广泛和更有效的临床应用和新的研究应用打开大门。分子影像学有可能成为诊断和研究神经退行性疾病以及指导治疗的标准和基本临床及研究工具。在这条道路上,我们将需要重新定义分子影像学相对于新兴的基于血液的生物标志物的作用。总的来说,分子影像学的独特特征——即有可能提供活体中分子病理过程的存在、程度、定位和数量的直接非侵入性信息——以及预测的新型示踪剂和成像技术的发展,为这种改善神经退行性疾病的诊疗和研究的方法带来了光明的前景。