痴呆的分子影像学研究

Jens Kurth , Monique Sakretz , Stefan Teipel , Bernd Joachim Krause
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引用次数: 18

摘要

在过去的一个世纪里,由于医疗保健的改善,人口的年龄不断增加,导致痴呆症患者人数增加。然而,通过适当的支持和对症治疗,许多患者可以继续拥有积极的生活和良好的生活质量。如果在早期阶段应用治疗和支持,效果最好,而且新的疾病改善治疗需要关注痴呆症前期和症状前阶段的疾病。本文重点介绍了分子神经成像生物标志物在老年痴呆症、路易体痴呆和额颞叶变性等不同形式痴呆的早期可靠临床诊断中的作用。这些不同类型的痴呆与F-18-FDG PET中代谢低下的特征性模式相关。这些减少在症状出现前几年就已经发生,并且与临床严重程度密切相关。最近开发的淀粉样蛋白- pet示踪剂有望在不久的将来成为描述AD早期阶段的有效工具。由于新的治疗方法,它们也可以直接监测淀粉样蛋白负荷的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular imaging of dementia

The increasing age of the population due to improvements in health care in the past century contributes to an increase in the number of people with dementia. However, with an appropriate support and symptomatic treatment, many patients can continue to have an active life and a good quality of life. Treatment and support work best if they are applied at an early stage and also new disease modifying treatments need to focus on predementia and presymptomatic stages of disease.

This article focuses on the role of molecular neuroimaging biomarkers in the reliable clinical diagnosis of dementia at the earliest possible stage of different forms of dementia like Alzheimer's disease, Dementia with Lewy Bodies and frontotemporal lobar degeneration. These different types of dementia are associated with characteristic patterns of hypometabolism in F-18-FDG PET. These reductions occur already years before the onset of symptoms and are strongly correlated with clinical severity.

Recently developed Amyloid-PET-tracers hold promises to be efficient tools in the near future to depict the earliest stages of AD. They may also serve to directly monitor changes of amyloid load due to new treatment approaches.

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