Jack Clifford R, Graf Ana, Burnham Samantha C, Doty Erin G, Moebius Hans J, Montenigro Philip, Siemers Eric, Sink Kaycee M, Shaw Leslie M, Hansen Charlotte Thim, Wildsmith Kristin R, Mahinrad Simin, Carrillo Maria C, Weber Christopher J
Department of Neurology Mayo Clinic Rochester Minnesota USA.
Novartis Pharma AG Basel Switzerland.
Alzheimers Dement (N Y). 2024 Dec 14;10(4):e70013. doi: 10.1002/trc2.70013. eCollection 2024 Oct-Dec.
The newly proposed revised criteria for diagnosis and staging of Alzheimer's disease (AD) by the Alzheimer's Association (AA) Workgroup represent a significant milestone in the field. These criteria offer objective measures for diagnosing and staging biological AD, bridging the gap between research and clinical care. Although implementation feasibility may vary across regions and settings, improving the availability and accuracy of biomarkers, especially plasma biomarkers, is expected to enhance the applicability of these criteria in clinical practice. The Fall 2023 Alzheimer's Association Research Roundtable (AARR) meeting served as a forum for gathering industry perspectives and feedback on these revised criteria, ensuring that the new criteria inform research, clinical trial design, and clinical care. In this article, we outline a summary of the newly proposed "Revised Criteria for Diagnosis and Staging of AD: AA Workgroup" and provide highlights from the AARR meeting in fall 2023.
The Alzheimer's Association Research Roundtable (AARR) convened leaders from industry, academia, and government, to review the , and gather industry perspectives and feedback on these revised criteria before its publication.The newly proposed revised criteria for diagnosis and staging of Alzheimer's disease (AD) by the AA's Workgroup represent a significant milestone, offering objective measures for the biological and staging of AD and bridging the gap between research and clinical care.Improving the availability and accuracy of biomarkers, especially blood-based biomarkers (BBMs) is expected to improve clinical research and enhance the applicability of these criteria in clinical practice.
阿尔茨海默病协会(AA)工作组新提出的阿尔茨海默病(AD)诊断和分期修订标准是该领域的一个重要里程碑。这些标准为生物性AD的诊断和分期提供了客观指标,弥合了研究与临床护理之间的差距。尽管实施可行性可能因地区和环境而异,但提高生物标志物,尤其是血浆生物标志物的可及性和准确性,有望增强这些标准在临床实践中的适用性。2023年秋季阿尔茨海默病协会研究圆桌会议(AARR)作为一个论坛,收集了行业对这些修订标准的观点和反馈,确保新标准为研究、临床试验设计和临床护理提供信息。在本文中,我们概述了新提出的“AD诊断和分期修订标准:AA工作组”的要点,并介绍了2023年秋季AARR会议的亮点。
阿尔茨海默病协会研究圆桌会议(AARR)召集了行业、学术界和政府的领导人,在新标准发布前对其进行审查,并收集行业对这些修订标准的观点和反馈。AA工作组新提出的阿尔茨海默病(AD)诊断和分期修订标准是一个重要里程碑,为AD的生物学诊断和分期提供了客观指标,弥合了研究与临床护理之间的差距。提高生物标志物,尤其是基于血液的生物标志物(BBM)的可及性和准确性,有望改善临床研究并增强这些标准在临床实践中的适用性。