Kong Yanyan, Zhang Shibo, Huang Lin, Zhang Chencheng, Xie Fang, Zhang Zhengwei, Huang Qi, Jiang Donglang, Li Junpeng, Zhou Weiyan, Hua Tao, Sun Bomin, Wang Jiao, Guan Yihui
PET Center, Huashan Hospital, Fudan University, Shanghai, China.
Laboratory of Molecular Neural Biology, School of Life Sciences, Shanghai University, Shanghai, China.
Front Aging Neurosci. 2021 Nov 2;13:731114. doi: 10.3389/fnagi.2021.731114. eCollection 2021.
Alzheimer's disease (AD) is the most common neurodegenerative disorder seen in age-dependent dementia. There is currently no effective treatment for AD, which may be attributed in part to lack of a clear underlying mechanism. Early diagnosis of AD is of great significance to control the development of the disease. Synaptic loss is an important pathology in the early stage of AD, therefore the measurement of synaptic density using molecular imaging technology may be an effective way to early diagnosis of AD. Synaptic vesicle glycoprotein 2A (SV2A) is located in the presynaptic vesicle membrane of virtually all synapses. SV2A Positron Emission Computed Tomography (PET) could provide a way to measure synaptic density quantitatively in living humans and to track changes in synaptic density in AD. In view of the fact that synaptic loss is the pathology of both epilepsy and AD, this review summarizes the potential role of SV2A in the pathogenesis of AD, and suggests that SV2A should be used as an important target molecule of PET imaging agent for the early diagnosis of AD.
阿尔茨海默病(AD)是年龄相关性痴呆中最常见的神经退行性疾病。目前尚无针对AD的有效治疗方法,这可能部分归因于缺乏明确的潜在机制。AD的早期诊断对于控制疾病发展具有重要意义。突触丢失是AD早期的重要病理学特征,因此利用分子成像技术测量突触密度可能是早期诊断AD的有效方法。突触囊泡糖蛋白2A(SV2A)几乎存在于所有突触的突触前囊泡膜中。SV2A正电子发射计算机断层显像(PET)能够提供一种在活体人类中定量测量突触密度以及追踪AD中突触密度变化的方法。鉴于突触丢失是癫痫和AD的共同病理学特征,本综述总结了SV2A在AD发病机制中的潜在作用,并提出SV2A应作为PET显像剂的重要靶点分子用于AD的早期诊断。