阿尔茨海默病的生物流体生物标志物:过去、现在和未来。

Medical review (Berlin, Germany) Pub Date : 2024-10-17 eCollection Date: 2024-12-01 DOI:10.1515/mr-2023-0071
Chengyu An, Huimin Cai, Ziye Ren, Xiaofeng Fu, Shuiyue Quan, Longfei Jia
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引用次数: 0

摘要

阿尔茨海默病(AD)是一种逐渐进行性的神经退行性疾病,具有巨大的社会和经济负担。因此,早期准确的诊断对于有效的治疗或预防疾病至关重要。脑脊液和血液生物标志物由于其相对可及性和广泛临床应用的潜力而成为有利的诊断工具。本文综述了AT(N)生物标志物系统,包括反映AD核心病理、淀粉样蛋白沉积、病理性tau以及神经变性的生物标志物。与炎症/免疫、突触功能障碍、血管病理和α-突触核蛋白病变相关的新型生物标志物也被讨论,这些生物标志物可能与AD的发病机制或临床进展有关。其他新兴的候选物,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的生物流体生物标志物景观。此外,本文还讨论了目前生物流体生物标志物在AD诊断中的挑战,并对未来的发展前景提出了见解。
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Biofluid biomarkers for Alzheimer's disease: past, present, and future.

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.

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