阿尔茨海默病(AD),最常见的痴呆症,尽管进行了数十年的研究和临床研究,但理解和治疗仍然具有挑战性。这可能部分是由于缺乏广泛可用且具有成本效益的诊断和预后方式。最近,基于血液的AD生物标志物领域在技术进步的推动下取得了重大进展,主要提高了分析和测量平台的分析灵敏度和精度。几种基于血液的生物标志物已显示出准确检测AD病理生理学的高潜力。因此,已经有相当大的兴趣应用这些生物标志物用于诊断和预后,作为替代指标,以研究各种协变量对AD病理生理学的影响,并加速AD治疗试验和监测治疗效果。然而,如何收集和收集血液样本缺乏标准化,已处理,存储的分析和报告可能会影响这些生物标志物测量的可重复性,可能会阻碍它们在临床和研究环境中的广泛使用。为了帮助解决这些问题,我们根据最近的研究结果,就样本处理对血液生物标志物测量的影响提供了基本指南.这些指南涵盖了重要的考虑因素,包括研究设计,采血,血液处理,生物缓冲,生物标志物测量,和结果报告。此外,拟议的指南包括用于遗传和核糖核酸分析的适当血液处理程序的最佳实践。虽然我们专注于AT(N)标准的关键基于血液的AD生物标志物(例如,淀粉样β[Aβ]40,Aβ42,Aβ42/40比例,total-tau,磷酸化-tau,神经丝轻链,脑源性tau和神经胶质原纤维酸性蛋白),我们预计这些指南将普遍适用于其他类型的血液生物标志物.我们还预计,这些指南将有助于研究人员规划和执行生物标志物研究,实现样品处理的统一,以提高研究之间的可比性。
Alzheimer\'s disease (AD), the most common form of dementia, remains challenging to understand and treat despite decades of research and clinical investigation. This might be partly due to a lack of widely available and cost-effective modalities for diagnosis and prognosis. Recently, the blood-based AD biomarker field has seen significant progress driven by technological advances, mainly improved analytical sensitivity and precision of the assays and measurement platforms. Several blood-based biomarkers have shown high potential for accurately detecting AD pathophysiology. As a result, there has been considerable interest in applying these biomarkers for diagnosis and prognosis, as surrogate metrics to investigate the impact of various covariates on AD pathophysiology and to accelerate AD therapeutic trials and monitor treatment effects. However, the lack of standardization of how blood samples and collected, processed, stored analyzed and reported can affect the reproducibility of these biomarker measurements, potentially hindering progress toward their widespread use in clinical and research settings. To help address these issues, we provide fundamental
guidelines developed according to recent research findings on the impact of sample handling on blood biomarker measurements. These
guidelines cover important considerations including study design, blood collection, blood processing, biobanking, biomarker measurement, and result reporting. Furthermore, the proposed
guidelines include best practices for appropriate blood handling procedures for genetic and ribonucleic acid analyses. While we focus on the key blood-based AD biomarkers for the AT(N) criteria (e.g., amyloid-beta [Aβ]40, Aβ42, Aβ42/40 ratio, total-tau, phosphorylated-tau, neurofilament light chain, brain-derived tau and glial fibrillary acidic protein), we anticipate that these
guidelines will generally be applicable to other types of blood biomarkers. We also anticipate that these
guidelines will assist investigators in planning and executing biomarker research, enabling harmonization of sample handling to improve comparability across studies.