Yi Zhang, Kefan Bi, Linfu Zhou, Jie Wang, Lingtong Huang, Yan Sun, Guoping Peng, Wei Wu
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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. 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引用次数: 0
摘要
阿尔茨海默病是一种神经退行性疾病,会逐渐降低认知能力,因此已成为公共卫生领域的一个重要问题。阿兹海默症被认为是一种持续恶化且目前无法治愈的疾病,它凸显了早期诊断和干预以延缓智力功能衰退的必要性。尽管脑脊液和正电子发射断层扫描技术在诊断注意力缺失症方面的疗效已得到证实,但这些技术的高成本和侵入性限制了其更广泛的应用。因此,血液生物标志物(如淀粉样蛋白-β、磷酸化陶氏体、总陶氏体等)以其高灵敏度、微创性、可及性和成本效益等特点,成为诊断 AD 的一个有前途的途径。超灵敏检测方法的出现,包括单分子酶联免疫吸附测定法和免疫沉淀-质谱法,彻底改变了 AD 血浆生物标志物的检测方法,取代了以前的低灵敏度技术。检测技术的飞速发展有助于更准确地量化血液中的病理性脑蛋白和注意力缺失症相关生物标志物。本手稿以美国国家老龄化研究所-阿尔茨海默氏症协会AT(N)研究框架为基础,细致回顾了当前有关AD免疫标志物的研究概况。它重点介绍了目前评估阿兹海默症血液免疫标志物不可或缺的前沿超灵敏检测技术。此外,这篇综述还探讨了对研究成果有重大影响的 AD 血液样本分析前处理的关键步骤,并讨论了临床检测过程中面临的实际挑战。这些讨论对于提高我们的理解力和利用血液生物标记物完善对 AD 的诊断精度至关重要。本综述旨在阐明检测和研究 AD 所用技术的潜在创新和改进途径,从而为更广泛的神经退行性疾病研究领域做出贡献。
Advances in Blood Biomarkers for Alzheimer's Disease: Ultra-Sensitive Detection Technologies and Impact on Clinical Diagnosis.
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.