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淀粉样蛋白成像的预后价值。

The prognostic value of amyloid imaging.

机构信息

Department of Neurology and Nuclear Medicine, University of Milano-Bicocca, Monza, Italy.

出版信息

Eur J Nucl Med Mol Imaging. 2012 Jul;39(7):1207-19. doi: 10.1007/s00259-012-2108-x. Epub 2012 Apr 11.

Abstract

Mild cognitive impairment is characterized by a decline in cognitive performance without interference with activities of daily living. The amnestic subtype of mild cognitive impairment progresses to Alzheimer's disease at a rate of 10-15% per year and in the majority the neuropathology is intermediate between the neuropathological changes of typical ageing and Alzheimer's disease. Amyloid deposition occurs over a decade before the development of noticeable cognitive symptoms in a continuous process that starts in healthy elderly individuals. Newly developed PET amyloid imaging agents provide noninvasive biomarkers for the early in vivo detection of Alzheimer's pathology in healthy elderly individuals and those with mild cognitive impairment. Exclusion of amyloid pathology should allow a more accurate prognosis to be given and ensure appropriate recruitment into clinical trials testing the efficacy of new putative antiamyloid agents at an earlier disease stage. The development of (18)F-labelled amyloid imaging agents has increased the availability of this new technology for clinical and research use since they can be used in PET centres where a cyclotron and radiochemistry are not available. This review discusses the role of PET imaging for assessing the amyloid load in cognitively normal elderly subjects and subjects with mild cognitive impairment at risk of conversion to Alzheimer's disease.

摘要

轻度认知障碍的特点是认知表现下降,而日常生活活动不受影响。遗忘型轻度认知障碍每年以 10-15%的速度进展为阿尔茨海默病,大多数患者的神经病理学介于典型衰老和阿尔茨海默病的神经病理学变化之间。淀粉样蛋白沉积在出现明显认知症状前 10 多年就开始了,这是一个从健康老年人开始的连续过程。新开发的 PET 淀粉样蛋白成像剂为在健康老年人和轻度认知障碍患者中早期体内检测阿尔茨海默病病理学提供了非侵入性生物标志物。排除淀粉样蛋白病理学可以更准确地预测预后,并确保在疾病早期阶段适当招募到临床试验中,以测试新的潜在抗淀粉样蛋白药物的疗效。由于(18)F 标记的淀粉样蛋白成像剂可在没有回旋加速器和放射化学的 PET 中心使用,因此增加了这项新技术在临床和研究中的可用性。这篇综述讨论了 PET 成像在评估认知正常的老年受试者和有转化为阿尔茨海默病风险的轻度认知障碍受试者的淀粉样蛋白负荷中的作用。

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