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痴呆谱系障碍:从数十年的 PET 研究中吸取的经验教训。

Dementia spectrum disorders: lessons learnt from decades with PET research.

机构信息

Neurodegeneration Imaging Group, Maurice Wohl Clinical Neuroscience Institute, 125 Coldharbour Lane, Camberwell, London, SE5 9NU, UK.

出版信息

J Neural Transm (Vienna). 2019 Mar;126(3):233-251. doi: 10.1007/s00702-019-01975-4. Epub 2019 Feb 14.

Abstract

The dementia spectrum encompasses a range of disorders with complex diagnosis, pathophysiology and limited treatment options. Positron emission tomography (PET) imaging provides insights into specific neurodegenerative processes underlying dementia disorders in vivo. Here we focus on some of the most common dementias: Alzheimer's disease, Parkinsonism dementias including Parkinson's disease with dementia, dementia with Lewy bodies, progressive supranuclear palsy and corticobasal syndrome, and frontotemporal lobe degeneration. PET tracers have been developed to target specific proteinopathies (amyloid, tau and α-synuclein), glucose metabolism, cholinergic system and neuroinflammation. Studies have shown distinct imaging abnormalities can be detected early, in some cases prior to symptom onset, allowing disease progression to be monitored and providing the potential to predict symptom onset. Furthermore, advances in PET imaging have identified potential therapeutic targets and novel methods to accurately discriminate between different types of dementias in vivo. There are promising imaging markers with a clinical application on the horizon, however, further studies are required before they can be implantation into clinical practice.

摘要

痴呆谱系包括一系列具有复杂诊断、病理生理学和有限治疗选择的疾病。正电子发射断层扫描 (PET) 成像提供了对痴呆症中潜在神经退行性过程的深入了解。在这里,我们重点介绍一些最常见的痴呆症:阿尔茨海默病、帕金森病痴呆症,包括伴有痴呆的帕金森病、路易体痴呆症、进行性核上性麻痹和皮质基底节综合征,以及额颞叶变性。已经开发了 PET 示踪剂来靶向特定的蛋白病(淀粉样蛋白、tau 和 α-突触核蛋白)、葡萄糖代谢、胆碱能系统和神经炎症。研究表明,在某些情况下,在症状出现之前就可以早期检测到不同的影像学异常,从而可以监测疾病进展,并有可能预测症状出现。此外,PET 成像的进展已经确定了潜在的治疗靶点和新的方法,可以在体内准确区分不同类型的痴呆症。有一些有前途的成像标志物具有临床应用前景,但在将其应用于临床实践之前,还需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc84/6449308/04887ab0377d/702_2019_1975_Fig1_HTML.jpg

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