An Chengyu, Cai Huimin, Ren Ziye, Fu Xiaofeng, Quan Shuiyue, Jia Longfei
Innovation Center for Neurological Disorders and Department of Neurology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, Beijing, China.
Med Rev (2021). 2024 Oct 17;4(6):467-491. doi: 10.1515/mr-2023-0071. eCollection 2024 Dec.
Alzheimer's disease (AD) is a gradually progressive neurodegenerative disease with tremendous social and economic burden. Therefore, early and accurate diagnosis is imperative for effective treatment or prevention of the disease. Cerebrospinal fluid and blood biomarkers emerge as favorable diagnostic tools due to their relative accessibility and potential for widespread clinical use. This review focuses on the AT(N) biomarker system, which includes biomarkers reflecting AD core pathologies, amyloid deposition, and pathological tau, as well as neurodegeneration. Novel biomarkers associated with inflammation/immunity, synaptic dysfunction, vascular pathology, and α-synucleinopathy, which might contribute to either the pathogenesis or the clinical progression of AD, have also been discussed. Other emerging candidates including non-coding RNAs, metabolites, and extracellular vesicle-based markers have also enriched the biofluid biomarker landscape for AD. Moreover, the review discusses the current challenges of biofluid biomarkers in AD diagnosis and offers insights into the prospective future development.
阿尔茨海默病(AD)是一种渐进性神经退行性疾病,带来了巨大的社会和经济负担。因此,早期准确诊断对于有效治疗或预防该疾病至关重要。脑脊液和血液生物标志物因其相对易于获取以及广泛临床应用的潜力,成为了有利的诊断工具。本综述聚焦于AT(N)生物标志物系统,该系统包括反映AD核心病理、淀粉样蛋白沉积、病理性tau以及神经退行性变的生物标志物。还讨论了与炎症/免疫、突触功能障碍、血管病理和α-突触核蛋白病相关的新型生物标志物,这些可能对AD的发病机制或临床进展有影响。其他新兴候选物,包括非编码RNA、代谢物和基于细胞外囊泡的标志物,也丰富了AD生物流体生物标志物的领域。此外,本综述讨论了生物流体生物标志物在AD诊断中的当前挑战,并对未来的发展前景提供了见解。