Lu Xiuhong, Ji Bin, Huang Gang, Ding Hong
Shanghai Key Laboratory of Molecular Imaging, Jiading District Central Hospital Affiliated Shanghai University of Medicine and Health Sciences, Shanghai 201318, China.
School of pharmacy, Shanghai University of Medicine and Health Sciences, Shanghai 201318, China.
Fundam Res. 2024 Apr 21;5(1):63-71. doi: 10.1016/j.fmre.2024.04.013. eCollection 2025 Jan.
Dementia is characterized by synaptic and neuronal dysfunction in disease-specific brain regions. Repeated failure of dementia clinical trials with therapeutic drugs targeting abnormal protein aggregates has caused researchers to shift their focus to synaptic functions and increased the importance of clinically available imaging for synaptic density and the development of synapse-targeted intervention. Synaptic density imaging with positron emission tomography (PET) tracer enables non-invasive detection of synaptic loss and hence investigates the association with other neuropathological events exemplified by disease-specific abnormal protein accumulation. Many studies have reviewed the progress of synaptic density imaging; however, to our knowledge, there is no article yet that summarizes the research progress of multimodal imaging of synaptic density tracers combined with other dementia biomarkers. Moreover, synaptic function intervention for dementia therapy has not yet been summarized. In this review, first we detail the progress of synaptic density imaging including tracer development and preclinical/clinical application, followed by a discussion of multimodal imaging of synaptic density tracers combined with classic dementia biomarkers in the clinical research stage. Finally, we briefly summarize the synapse-targeted drugs for dementia therapy.
痴呆症的特征是特定疾病脑区的突触和神经元功能障碍。针对异常蛋白质聚集体的治疗药物在痴呆症临床试验中屡屡失败,这使得研究人员将重点转向突触功能,并提高了临床可用成像技术在检测突触密度以及开发突触靶向干预措施方面的重要性。使用正电子发射断层扫描(PET)示踪剂进行突触密度成像能够非侵入性地检测突触丢失,从而研究其与其他神经病理事件(如特定疾病的异常蛋白质积累)之间的关联。许多研究综述了突触密度成像的进展;然而,据我们所知,尚无文章总结突触密度示踪剂与其他痴呆生物标志物联合的多模态成像研究进展。此外,尚未对用于痴呆症治疗的突触功能干预进行总结。在本综述中,我们首先详细介绍突触密度成像的进展,包括示踪剂开发以及临床前/临床应用,随后讨论在临床研究阶段突触密度示踪剂与经典痴呆生物标志物联合的多模态成像。最后,我们简要总结用于痴呆症治疗的突触靶向药物。