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阿尔茨海默病生物标志物及其在临床研究与实践中的当前应用。

Alzheimer's disease biomarkers and their current use in clinical research and practice.

作者信息

Hunter Tai R, Santos Luis E, Tovar-Moll Fernanda, De Felice Fernanda G

机构信息

Department of Biomedical and Molecular Sciences, Queen's University, Kingston, ON, Canada.

D'Or Institute for Research and Education, Rio de Janeiro, RJ, Brazil.

出版信息

Mol Psychiatry. 2025 Jan;30(1):272-284. doi: 10.1038/s41380-024-02709-z. Epub 2024 Sep 4.

Abstract

While blood-based tests are readily available for various conditions, including cardiovascular diseases, type 2 diabetes, and common cancers, Alzheimer's disease (AD) and other neurodegenerative diseases lack an early blood-based screening test that can be used in primary care. Major efforts have been made towards the investigation of approaches that may lead to minimally invasive, cost-effective, and reliable tests capable of measuring brain pathological status. Here, we review past and current technologies developed to investigate biomarkers of AD, including novel blood-based approaches and the more established cerebrospinal fluid and neuroimaging biomarkers of disease. The utility of blood as a source of AD-related biomarkers in both clinical practice and interventional trials is discussed, supported by a comprehensive list of clinical trials for AD drugs and interventions that list biomarkers as primary or secondary endpoints. We highlight that identifying individuals in early preclinical AD using blood-based biomarkers will improve clinical trials and the optimization of therapeutic treatments as they become available. Lastly, we discuss challenges that remain in the field and address new approaches being developed, such as the examination of cargo packaged within extracellular vesicles of neuronal origin isolated from peripheral blood.

摘要

虽然基于血液的检测可用于多种病症,包括心血管疾病、2型糖尿病和常见癌症,但阿尔茨海默病(AD)和其他神经退行性疾病缺乏一种可用于初级保健的早期基于血液的筛查检测。人们已付出巨大努力来研究各种方法,以期开发出微创、经济高效且可靠的检测手段,用于测量脑部病理状态。在此,我们回顾过去和当前为研究AD生物标志物而开发的技术,包括新型基于血液的方法以及更成熟的脑脊液和神经影像疾病生物标志物。文中讨论了血液作为AD相关生物标志物来源在临床实践和干预试验中的效用,并列出了以生物标志物为主要或次要终点的AD药物和干预措施的综合临床试验清单作为支撑。我们强调,利用基于血液的生物标志物识别临床前AD早期阶段的个体,将改善临床试验以及治疗方法可用时的优化治疗。最后,我们讨论了该领域仍然存在的挑战,并阐述了正在开发的新方法,例如对外周血中分离出的神经元来源细胞外囊泡内包裹物质的检测。

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