Zhang Yi, Bi Kefan, Zhou Linfu, Wang Jie, Huang Lingtong, Sun Yan, Peng Guoping, Wu Wei
Department of Laboratory Medicine, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, People's Republic of China.
State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, National Medical Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, People's Republic of China.
Degener Neurol Neuromuscul Dis. 2024 Jul 30;14:85-102. doi: 10.2147/DNND.S471174. eCollection 2024.
Alzheimer's disease has escalated into a critical public health concern, marked by its neurodegenerative nature that progressively diminishes cognitive abilities. Recognized as a continuously advancing and presently incurable condition, AD underscores the necessity for early-stage diagnosis and interventions aimed at delaying the decline in mental function. Despite the proven efficacy of cerebrospinal fluid and positron emission tomography in diagnosing AD, their broader utility is constrained by significant costs and the invasive nature of these procedures. Consequently, the innovation of blood biomarkers such as Amyloid-beta, phosphorylated-tau, total-tau et al, distinguished by their high sensitivity, minimal invasiveness, accessibility, and cost-efficiency, emerges as a promising avenue for AD diagnosis. The advent of ultra-sensitive detection methodologies, including single-molecule enzyme-linked immunosorbent assay and immunoprecipitation-mass spectrometry, has revolutionized the detection of AD plasma biomarkers, supplanting previous low-sensitivity techniques. This rapid advancement in detection technology facilitates the more accurate quantification of pathological brain proteins and AD-associated biomarkers in the bloodstream. This manuscript meticulously reviews the landscape of current research on immunological markers for AD, anchored in the National Institute on Aging-Alzheimer's Association AT(N) research framework. It highlights a selection of forefront ultra-sensitive detection technologies now integral to assessing AD blood immunological markers. Additionally, this review examines the crucial pre-analytical processing steps for AD blood samples that significantly impact research outcomes and addresses the practical challenges faced during clinical testing. These discussions are crucial for enhancing our comprehension and refining the diagnostic precision of AD using blood-based biomarkers. The review aims to shed light on potential avenues for innovation and improvement in the techniques employed for detecting and investigating AD, thereby contributing to the broader field of neurodegenerative disease research.
阿尔茨海默病已升级为一个关键的公共卫生问题,其特征是具有神经退行性本质,会逐渐削弱认知能力。作为一种持续发展且目前无法治愈的病症,阿尔茨海默病凸显了早期诊断以及旨在延缓心理功能衰退的干预措施的必要性。尽管脑脊液和正电子发射断层扫描在诊断阿尔茨海默病方面已被证明有效,但其更广泛的应用受到高昂成本和这些检查的侵入性的限制。因此,诸如淀粉样蛋白β、磷酸化tau蛋白、总tau蛋白等血液生物标志物的创新,因其高灵敏度、微创性、易获取性和成本效益而成为阿尔茨海默病诊断的一个有前景的途径。包括单分子酶联免疫吸附测定和免疫沉淀 - 质谱分析在内的超灵敏检测方法的出现,彻底改变了阿尔茨海默病血浆生物标志物的检测,取代了以前低灵敏度的技术。检测技术的这一快速发展有助于更准确地定量血液中病理性脑蛋白和与阿尔茨海默病相关的生物标志物。本手稿以美国国立衰老研究所 - 阿尔茨海默病协会(AT(N))研究框架为基础,精心回顾了当前关于阿尔茨海默病免疫标志物的研究情况。它突出了一系列前沿的超灵敏检测技术,这些技术现在对于评估阿尔茨海默病血液免疫标志物不可或缺。此外,本综述探讨了对阿尔茨海默病血液样本至关重要的分析前处理步骤,这些步骤会显著影响研究结果,并解决了临床检测过程中面临的实际挑战。这些讨论对于增强我们对使用基于血液的生物标志物诊断阿尔茨海默病的理解以及提高诊断精度至关重要。该综述旨在阐明在用于检测和研究阿尔茨海默病的技术方面潜在的创新和改进途径,从而为神经退行性疾病研究的更广泛领域做出贡献。