Amyloid imaging in dementia

Azhaar Ashraf, P. Mehta, P. Edison
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引用次数: 2

Abstract

A major advancement in the field of medicine has been the timely advent of amyloid imaging, which has allowed critical evaluation of the complex relationship between amyloid β peptide (Aβ) aggregation and Alzheimer's disease in vivo . Most importantly, amyloid imaging has the potential to detect Aβ in mildly affected as well as asymptomatic individuals, when the therapeutic window of opportunity might still be open to pharmacological intervention. It also shows significant promise in differential diagnosis of mild cognitive impairment or atypical dementias. Amyloid imaging studies support a model in which amyloid aggregation is considered an early event on the path of dementia, beginning insidiously in cognitively healthy individuals being accompanied by subtle cognitive, functional and structural brain alterations suggestive of incipient AD. As individuals progress to dementia, clinical decline and neurodegeneration accelerate and might proceed independently of amyloid accumulation. In this review we focus on amyloid imaging with particular emphasis on [ 11 C]PIB in AD, mild cognitive impairment and other dementias, and discuss the advances made in this perplexing field.
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痴呆中的淀粉样蛋白成像
淀粉样蛋白成像的及时出现是医学领域的一个重大进步,它使得对体内淀粉样蛋白β肽(Aβ)聚集与阿尔茨海默病之间复杂关系的关键评估成为可能。最重要的是,淀粉样蛋白成像有可能在轻度影响和无症状的个体中检测到Aβ,当治疗机会之窗可能仍然对药物干预开放时。它在轻度认知障碍或非典型痴呆的鉴别诊断中也显示出显著的前景。淀粉样蛋白成像研究支持一种模型,即淀粉样蛋白聚集被认为是痴呆路径上的一个早期事件,在认知健康的个体中悄然开始,伴随着提示早期AD的微妙认知、功能和大脑结构改变。当个体进展为痴呆时,临床衰退和神经退行性变加速,并且可能独立于淀粉样蛋白积累进行。在这篇综述中,我们将重点关注淀粉样蛋白成像,特别强调[11 C]PIB在AD、轻度认知障碍和其他痴呆症中的应用,并讨论这一令人困惑的领域的进展。
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