College of Pharmacy, Shenzhen Technology University, Shenzhen, China.
Department of Pharmacy, Shenzhen People's Hospital (The Second Clinical Medical College, The First Affiliated Hospital, Jinan University, Southern University of Science and Technology), Shenzhen, China.
CNS Neurosci Ther. 2024 Nov;30(11):e70060. doi: 10.1111/cns.70060.
Diagnosis and prediction of Alzheimer's disease (AD) are increasingly pressing in the early stage of the disease because the biomarker-targeted therapies may be most effective. Diagnosis of AD largely depends on the clinical symptoms of AD. Currently, cerebrospinal fluid biomarkers and neuroimaging techniques are considered for clinical detection and diagnosis. However, these clinical diagnosis results could provide indications of the middle and/or late stages of AD rather than the early stage, and another limitation is the complexity attached to limited access, cost, and perceived invasiveness. Therefore, the prediction of AD still poses immense challenges, and the development of novel biomarkers is needed for early diagnosis and urgent intervention before the onset of obvious phenotypes of AD. Blood-based biomarkers may enable earlier diagnose and aid detection and prognosis for AD because various substances in the blood are vulnerable to AD pathophysiology. The application of a systematic biological paradigm based on high-throughput techniques has demonstrated accurate alterations of molecular levels during AD onset processes, such as protein levels and metabolite levels, which may facilitate the identification of AD at an early stage. Notably, proteomics and metabolomics have been used to identify candidate biomarkers in blood for AD diagnosis. This review summarizes data on potential blood-based biomarkers identified by proteomics and metabolomics that are closest to clinical implementation and discusses the current challenges and the future work of blood-based candidates to achieve the aim of early screening for AD. We also provide an overview of early diagnosis, drug target discovery and even promising therapeutic approaches for AD.
阿尔茨海默病(AD)的诊断和预测在疾病早期变得越来越紧迫,因为针对生物标志物的治疗方法可能最有效。AD 的诊断在很大程度上取决于 AD 的临床症状。目前,脑脊液生物标志物和神经影像学技术被认为可用于临床检测和诊断。然而,这些临床诊断结果可能表明 AD 的中/晚期,而不是早期,另一个限制是由于获取受限、成本高和感知侵入性而带来的复杂性。因此,AD 的预测仍然面临巨大挑战,需要开发新的生物标志物,以便在 AD 明显表型出现之前进行早期诊断和紧急干预。基于血液的生物标志物可以实现更早的诊断,并有助于 AD 的检测和预后,因为血液中的各种物质容易受到 AD 病理生理学的影响。基于高通量技术的系统生物学范式的应用已经证明了 AD 发病过程中分子水平的准确改变,例如蛋白质水平和代谢物水平,这可能有助于在早期识别 AD。值得注意的是,蛋白质组学和代谢组学已被用于鉴定 AD 血液诊断的候选生物标志物。本综述总结了蛋白质组学和代谢组学鉴定的与临床实施最接近的潜在血液生物标志物的数据,并讨论了当前基于血液的候选物的挑战和未来工作,以实现 AD 的早期筛查目标。我们还概述了 AD 的早期诊断、药物靶点发现甚至有前途的治疗方法。