Rabinovici Gil D, Knopman David S, Arbizu Javier, Benzinger Tammie L S, Donohoe Kevin J, Hansson Oskar, Herscovitch Peter, Kuo Phillip H, Lingler Jennifer H, Minoshima Satoshi, Murray Melissa E, Price Julie C, Salloway Stephen P, Weber Christopher J, Carrillo Maria C, Johnson Keith A
Department of Neurology and Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, USA.
Mayo Clinic Neurology and Neurosurgery, Rochester, Minnesota, USA.
Alzheimers Dement. 2025 Jan;21(1):e14338. doi: 10.1002/alz.14338. Epub 2025 Jan 8.
The Alzheimer's Association and the Society of Nuclear Medicine and Molecular Imaging convened a multidisciplinary workgroup to update appropriate use criteria (AUC) for amyloid positron emission tomography (PET) and to develop AUC for tau PET.
The workgroup identified key research questions that guided a systematic literature review on clinical amyloid/tau PET. Building on this review, the workgroup developed 17 clinical scenarios in which amyloid or tau PET may be considered. A modified Delphi approach was used to rate each scenario by consensus as "rarely appropriate," "uncertain," or "appropriate." Ratings were performed separately for amyloid and tau PET as stand-alone modalities.
For amyloid PET, seven scenarios were rated as appropriate, two as uncertain, and eight as rarely appropriate. For tau PET, five scenarios were rated as appropriate, six as uncertain, and six as rarely appropriate.
AUC for amyloid and tau PET provide expert recommendations for clinical use of these technologies in the evolving landscape of diagnostics and therapeutics for Alzheimer's disease.
A multidisciplinary workgroup convened by the Alzheimer's Association and the Society of Nuclear Medicine and Molecular Imaging updated the appropriate use criteria (AUC) for amyloid positron emission tomography (PET) and to develop AUC for tau PET. The goal of these updated AUC is to assist clinicians in identifying clinical scenarios in which amyloid or tau PET may be useful for guiding the diagnosis and management of patients who have, or are at risk for, cognitive decline These updated AUC are intended for dementia specialists who spend a significant proportion of their clinical effort caring for patients with cognitive complaints, as well as serve as a general reference for a broader audience interested in implementation of amyloid and tau PET in clinical practice.
阿尔茨海默病协会与核医学和分子影像学会召集了一个多学科工作组,以更新淀粉样蛋白正电子发射断层扫描(PET)的合理使用标准(AUC),并制定tau PET的AUC。
该工作组确定了关键研究问题,这些问题指导了对临床淀粉样蛋白/tau PET的系统文献综述。在此综述的基础上,工作组制定了17种可能考虑使用淀粉样蛋白或tau PET的临床场景。采用改良的德尔菲法,通过共识将每个场景评为“极少适用”、“不确定”或“适用”。分别对作为独立检查手段的淀粉样蛋白PET和tau PET进行评级。
对于淀粉样蛋白PET,7种场景被评为适用,2种为不确定,8种为极少适用。对于tau PET,5种场景被评为适用,6种为不确定,6种为极少适用。
淀粉样蛋白和tau PET的AUC为这些技术在阿尔茨海默病诊断和治疗不断变化的格局中的临床应用提供了专家建议。
由阿尔茨海默病协会与核医学和分子影像学会召集的一个多学科工作组更新了淀粉样蛋白正电子发射断层扫描(PET)的合理使用标准(AUC),并制定了tau PET的AUC。这些更新后的AUC的目标是帮助临床医生识别淀粉样蛋白或tau PET可能有助于指导对有认知功能下降或有认知功能下降风险的患者进行诊断和管理的临床场景。这些更新后的AUC适用于将大量临床精力用于照顾有认知主诉患者的痴呆症专家,也可作为对有兴趣在临床实践中应用淀粉样蛋白和tau PET的更广泛受众的一般参考。