van der Molen Lennart H, Boenink Marianne, van Lente Harro, Richard Edo
IQ Health science department, Radboudumc, Nijmegen, The Netherlands.
Society Studies department, Maastricht University, Maastricht, The Netherlands.
Alzheimers Dement. 2025 Apr;21(4):e70133. doi: 10.1002/alz.70133.
Whether Alzheimer's disease (AD) should be defined by symptoms, biological processes, or both, is a matter of debate. We aim to reconstruct the motivations, aims, and content of consecutive versions of AD diagnostic criteria.
We systematically analyzed publications on AD diagnostic criteria between 1984 and 2024.
Early diagnosis and incorporating recent scientific findings are recurring aims for criteria revisions but aims and motivations for revising are often unclear or ambiguous and reflection on previous criteria is lacking. The subsequent criteria, except International Working Group (IWG) 2021/2024, consistently lower the threshold for diagnosing AD and increasingly focus on amyloid β and tau biomarkers.
Subsequent AD criteria show an increasing "biomarkerization," but it is often unclear what problems revised criteria should solve and how effective they are. To overcome these limitations, future revisions should evaluate the effectiveness and impacts of previous criteria, and define clear problems and aims.
Early diagnosis and incorporating scientific insights are recurring aims. The aims of new criteria are often not clearly articulated or ambiguous. The number of requirements for an AD diagnosis decreases over time. Consecutive criteria for research and clinical use did not result in clear terminology. The AD definition is increasingly narrowed to amyloid β and tau.
阿尔茨海默病(AD)应根据症状、生物学过程还是两者来定义,这是一个有争议的问题。我们旨在重构AD诊断标准连续版本的动机、目标和内容。
我们系统分析了1984年至2024年间关于AD诊断标准的出版物。
早期诊断和纳入最新科学发现是标准修订的反复出现的目标,但修订的目标和动机往往不明确或含糊不清,且缺乏对先前标准的反思。除国际工作组(IWG)2021/2024外,后续标准持续降低AD诊断阈值,并越来越关注淀粉样β蛋白和tau生物标志物。
后续的AD标准显示出越来越多的“生物标志物化”,但修订后的标准应解决哪些问题以及它们的有效性如何,往往并不明确。为克服这些局限性,未来的修订应评估先前标准的有效性和影响,并明确问题和目标。
早期诊断和纳入科学见解是反复出现的目标。新标准的目标往往表述不清晰或含糊不清。AD诊断的要求数量随时间减少。连续的研究和临床使用标准并未产生明确的术语。AD的定义越来越局限于淀粉样β蛋白和tau。