Cheng Qian, Fan Yiou, Zhang Pengfei, Liu Huan, Han Jialin, Yu Qian, Wang Xueying, Wu Shuang, Lu Zhiming
Department of Clinical Laboratory, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong 250021, China.
Laboratory and Quality Management Department, Centers for Disease Control and Prevention of Shandong, Jinan, Shandong, China.
Ageing Res Rev. 2025 Feb;104:102642. doi: 10.1016/j.arr.2024.102642. Epub 2024 Dec 17.
Synapse has been considered a critical neuronal structure in the procession of Alzheimer's disease (AD), attacked by two pathological molecule aggregates (amyloid-β and phosphorylated tau) in the brain, disturbing synaptic homeostasis before disease manifestation and subsequently causing synaptic degeneration. Recently, evidence has emerged indicating that soluble oligomeric amyloid-β (AβO) and tau exert direct toxicity on synapses, causing synaptic damage. Synaptic degeneration is closely linked to cognitive decline in AD, even in the asymptomatic stages of AD. Therefore, the identification of novel, specific, and sensitive biomarkers involved in synaptic degeneration holds significant promise for early diagnosis of AD, reducing synaptic degeneration and loss, and controlling the progression of AD. Currently, a range of biomarkers in cerebrospinal fluid (CSF), such as synaptosome-associated protein 25 (SNAP-25), synaptotagmin-1, growth-associated protein-43 (GAP-43), and neurogranin (Ng), along with functional brain imaging techniques, can detect variations in synaptic density, offering high sensitivity and specificity for AD diagnosis. However, these methods face challenges, including invasiveness, high cost, and limited accessibility. In contrast, biomarkers found in blood or urine provide a minimally invasive, cost-effective, and more accessible alternative to traditional diagnostic methods. Notably, neuron-derived exosomes in blood, which contain synaptic proteins, show variations in concentration that can serve as indicators of synaptic injury, providing an additional, less invasive approach to AD diagnosis and monitoring.
突触被认为是阿尔茨海默病(AD)进程中的关键神经元结构,在大脑中受到两种病理性分子聚集体(淀粉样β蛋白和磷酸化tau蛋白)的攻击,在疾病表现出来之前扰乱突触稳态,随后导致突触退化。最近,有证据表明可溶性寡聚淀粉样β蛋白(AβO)和tau蛋白对突触具有直接毒性,导致突触损伤。突触退化与AD的认知衰退密切相关,即使在AD的无症状阶段也是如此。因此,鉴定参与突触退化的新型、特异性和敏感的生物标志物对于AD的早期诊断、减少突触退化和损失以及控制AD的进展具有重大前景。目前,脑脊液(CSF)中的一系列生物标志物,如突触小体相关蛋白25(SNAP - 25)、突触结合蛋白 - 1、生长相关蛋白 - 43(GAP - 43)和神经颗粒素(Ng),以及功能性脑成像技术,可以检测突触密度的变化,为AD诊断提供高灵敏度和特异性。然而,这些方法面临挑战,包括侵入性、高成本和可及性有限。相比之下,血液或尿液中发现的生物标志物为传统诊断方法提供了一种微创、经济高效且更易获得的替代方案。值得注意的是,血液中神经元衍生的外泌体含有突触蛋白,其浓度变化可作为突触损伤的指标,为AD诊断和监测提供了另一种侵入性较小的方法。