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阿尔茨海默病诊断生物标志物验证的战略生物标志物路线图:方法学更新。

The strategic biomarker roadmap for the validation of Alzheimer's diagnostic biomarkers: methodological update.

机构信息

German Center for Neurodegenerative Diseases DZNE-Standort Rostock/Greifswald, Gehlsheimer Str. 20, 18147, Rostock, Germany.

LANVIE - Laboratory of Neuroimaging of Aging, University of Geneva, Geneva, Switzerland.

出版信息

Eur J Nucl Med Mol Imaging. 2021 Jul;48(7):2070-2085. doi: 10.1007/s00259-020-05120-2. Epub 2021 Mar 10.

Abstract

BACKGROUND

The 2017 Alzheimer's disease (AD) Strategic Biomarker Roadmap (SBR) structured the validation of AD diagnostic biomarkers into 5 phases, systematically assessing analytical validity (Phases 1-2), clinical validity (Phases 3-4), and clinical utility (Phase 5) through primary and secondary Aims. This framework allows to map knowledge gaps and research priorities, accelerating the route towards clinical implementation. Within an initiative aimed to assess the development of biomarkers of tau pathology, we revised this methodology consistently with progress in AD research.

METHODS

We critically appraised the adequacy of the 2017 Biomarker Roadmap within current diagnostic frameworks, discussed updates at a workshop convening the Alzheimer's Association and 8 leading AD biomarker research groups, and detailed the methods to allow consistent assessment of aims achievement for tau and other AD diagnostic biomarkers.

RESULTS

The 2020 update applies to all AD diagnostic biomarkers. In Phases 2-3, we admitted a greater variety of study designs (e.g., cross-sectional in addition to longitudinal) and reference standards (e.g., biomarker confirmation in addition to clinical progression) based on construct (in addition to criterion) validity. We structured a systematic data extraction to enable transparent and formal evidence assessment procedures. Finally, we have clarified issues that need to be addressed to generate data eligible to evidence-to-decision procedures.

DISCUSSION

This revision allows for more versatile and precise assessment of existing evidence, keeps up with theoretical developments, and helps clinical researchers in producing evidence suitable for evidence-to-decision procedures. Compliance with this methodology is essential to implement AD biomarkers efficiently in clinical research and diagnostics.

摘要

背景

2017 年阿尔茨海默病(AD)战略生物标志物路线图(SBR)将 AD 诊断生物标志物的验证分为 5 个阶段,通过主要和次要目标系统地评估分析有效性(第 1-2 阶段)、临床有效性(第 3-4 阶段)和临床实用性(第 5 阶段)。该框架允许映射知识差距和研究重点,加速向临床实施的路线。在一项旨在评估 tau 病理学生物标志物发展的倡议中,我们根据 AD 研究的进展对该方法进行了修订。

方法

我们批判性地评估了 2017 年生物标志物路线图在当前诊断框架中的充分性,在一次召集阿尔茨海默病协会和 8 个领先的 AD 生物标志物研究小组的研讨会讨论了更新内容,并详细说明了允许对 tau 和其他 AD 诊断生物标志物的目标实现进行一致评估的方法。

结果

2020 年的更新适用于所有 AD 诊断生物标志物。在第 2-3 阶段,我们根据构念(而不仅仅是标准)有效性,接受了更多种类的研究设计(例如,横断面研究除了纵向研究)和参考标准(例如,生物标志物的确认除了临床进展)。我们构建了一个系统的数据提取,以实现透明和正式的证据评估程序。最后,我们澄清了需要解决的问题,以生成有资格进行证据决策程序的数据。

讨论

这次修订允许更灵活和精确地评估现有证据,跟上理论发展,并帮助临床研究人员生成适合证据决策程序的数据。遵守该方法对于在临床研究和诊断中有效地实施 AD 生物标志物至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a91c/8175304/2615a6375713/259_2020_5120_Fig1_HTML.jpg

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