Department of Radiology, Mayo Clinic, Rochester, Minnesota
Department of Radiology, Mayo Clinic, Rochester, Minnesota.
J Nucl Med. 2024 Jun 3;65(6):829-837. doi: 10.2967/jnumed.123.266463.
Antiamyloid therapies for Alzheimer disease recently entered clinical practice, making imaging biomarkers for Alzheimer disease even more relevant to guiding patient management. Amyloid and tau PET are valuable tools that can provide objective evidence of Alzheimer pathophysiology in living patients and will increasingly be used to complement F-FDG PET in the diagnostic evaluation of cognitive impairment and dementia. Parkinsonian syndromes, also common causes of dementia, can likewise be evaluated with a PET imaging biomarker,F-DOPA, allowing in vivo assessment of the presynaptic dopaminergic neurons. Understanding the role of these PET biomarkers will help the nuclear medicine physician contribute to the appropriate diagnosis and management of patients with cognitive impairment and dementia. To successfully evaluate brain PET examinations for neurodegenerative diseases, knowledge of the necessary protocol details for obtaining a reliable imaging study, inherent limitations for each PET radiopharmaceutical, and pitfalls in image interpretation is critical. This review will focus on underlying concepts for interpreting PET examinations, important procedural details, and guidance for avoiding potential interpretive pitfalls for amyloid, tau, and dopaminergic PET examinations.
抗淀粉样蛋白疗法最近已进入临床实践,这使得阿尔茨海默病的影像学生物标志物对指导患者管理更为重要。淀粉样蛋白和 tau PET 是有价值的工具,可在活体患者中提供阿尔茨海默病病理生理学的客观证据,并将越来越多地与 F-FDG PET 一起用于认知障碍和痴呆的诊断评估。帕金森综合征也是常见的痴呆原因,同样可以使用 PET 成像生物标志物 F-DOPA 进行评估,从而可以在体内评估突触前多巴胺能神经元。了解这些 PET 生物标志物的作用将有助于核医学医师为认知障碍和痴呆患者的适当诊断和治疗做出贡献。为了成功评估神经退行性疾病的脑 PET 检查,了解获得可靠成像研究所需的协议细节、每种 PET 放射性药物的固有局限性以及图像解释中的陷阱至关重要。本综述将重点介绍解释 PET 检查的基本概念、重要的程序细节以及避免淀粉样蛋白、tau 和多巴胺 PET 检查中潜在解释陷阱的指导。