Leuzy Antoine, Bollack Ariane, Pellegrino Daniela, Teunissen Charlotte E, La Joie Renaud, Rabinovici Gil D, Franzmeier Nicolai, Johnson Keith, Barkhof Frederik, Shaw Leslie M, Arkhipenko Alexander, Schindler Suzanne E, Honig Lawrence S, Moscoso Rial Alexis, Schöll Michael, Zetterberg Henrik, Blennow Kaj, Hansson Oskar, Farrar Gill
Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Lund, Sweden.
Wallenberg Centre for Molecular and Translational Medicine, University of Gothenburg, Gothenburg, Sweden.
Alzheimers Dement. 2025 Mar;21(3):e14528. doi: 10.1002/alz.14528.
Amyloid-β (Aβ) positron emission tomography (PET) imaging and cerebrospinal fluid (CSF) biomarkers are now established tools in the diagnostic workup of patients with Alzheimer's disease (AD), and their use is anticipated to increase with the introduction of new disease-modifying therapies. Although these biomarkers are comparable alternatives in research settings to determine Aβ status, biomarker testing in clinical practice requires careful consideration of the strengths and limitations of each modality, as well as the specific clinical context, to identify which test is best suited for each patient. This article provides a comprehensive review of the pathologic processes reflected by Aβ-PET and CSF biomarkers, their performance, and their current and future applications and contexts of use. The primary aim is to assist clinicians in making better-informed decisions about the suitability of each biomarker in different clinical situations, thereby reducing the risk of misdiagnosis or incorrect interpretation of biomarker results. HIGHLIGHTS: Recent advances have positioned Aβ PET and CSF biomarkers as pivotal in AD diagnosis. It is crucial to understand the differences in the clinical use of these biomarkers. A team of experts reviewed the state of Aβ PET and CSF markers in clinical settings. Differential features in the clinical application of these biomarkers were reviewed. We discussed the role of Aβ PET and CSF in the context of novel plasma biomarkers.
淀粉样蛋白-β(Aβ)正电子发射断层扫描(PET)成像和脑脊液(CSF)生物标志物现已成为阿尔茨海默病(AD)患者诊断检查中的既定工具,随着新的疾病修饰疗法的引入,其使用预计会增加。尽管在研究环境中,这些生物标志物是确定Aβ状态的可比替代方法,但在临床实践中进行生物标志物检测需要仔细考虑每种检测方法的优势和局限性,以及具体的临床背景,以确定哪种检测最适合每位患者。本文全面综述了Aβ-PET和CSF生物标志物所反映的病理过程、它们的性能以及它们当前和未来的应用及使用背景。主要目的是帮助临床医生在不同临床情况下就每种生物标志物的适用性做出更明智的决策,从而降低生物标志物结果误诊或错误解读的风险。要点:最近的进展使Aβ PET和CSF生物标志物在AD诊断中占据关键地位。了解这些生物标志物在临床应用中的差异至关重要。一组专家回顾了Aβ PET和CSF标志物在临床环境中的状况。回顾了这些生物标志物在临床应用中的差异特征。我们讨论了Aβ PET和CSF在新型血浆生物标志物背景下的作用。