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AD 分子标志物:阿尔茨海默病的分子影像学:神经递质系统的正电子发射断层扫描成像。

AD molecular: Molecular imaging of Alzheimer's disease: PET imaging of neurotransmitter systems.

机构信息

Department of Psychiatry and Alzheimer's Disease Research Unit, Yale University School of Medicine, New Haven, CT, United States.

出版信息

Prog Mol Biol Transl Sci. 2019;165:139-165. doi: 10.1016/bs.pmbts.2019.04.003. Epub 2019 May 23.

Abstract

Current understanding of Alzheimer's disease (AD) pathogenesis relies on the observed accumulations of amyloid β and phosphorylated tau aggregates that are thought to play key roles in initiating or propagating disease. However, other processes including changes in synaptic proteins and neurotransmitter loss have been suggested as important etiologies or contributors. Positron emission tomography (PET) imaging allows in vivo investigations of molecular changes associated with AD. PET imaging with multiple radiotracers can be used in combination with other modalities such as magnetic resonance imaging (MRI), and with assessments of cognition and neuropsychiatric symptoms to investigate the molecular underpinnings of AD. Studies of synaptic protein changes may improve the understanding of disease mechanisms and provide valuable markers of disease progression and therapeutic efficacy. This chapter will illustrate the importance of in vivo molecular imaging in the study of AD with a specific emphasis on PET and radioligands for several non-amyloid targets.

摘要

目前对阿尔茨海默病(AD)发病机制的理解依赖于观察到的淀粉样β和磷酸化 tau 聚集物的积累,这些聚集物被认为在引发或传播疾病方面发挥着关键作用。然而,其他过程,包括突触蛋白的变化和神经递质的丧失,已被认为是重要的病因或促成因素。正电子发射断层扫描(PET)成像允许对与 AD 相关的分子变化进行体内研究。使用多种放射性示踪剂的 PET 成像可与磁共振成像(MRI)等其他模式结合使用,并与认知和神经精神症状评估相结合,以研究 AD 的分子基础。研究突触蛋白变化可能有助于更好地了解疾病机制,并为疾病进展和治疗效果提供有价值的标志物。本章将特别强调正电子发射断层扫描(PET)和几种非淀粉样蛋白靶标放射性配体,说明在 AD 研究中体内分子成像的重要性。

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