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首页> 外文期刊>Alzheimer’s & dementia: the journal of the Alzheimer’s Association >Amyloid-related imaging abnormalities in amyloid-modifying therapeutic trials: recommendations from the Alzheimer's Association Research Roundtable Workgroup.
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Amyloid-related imaging abnormalities in amyloid-modifying therapeutic trials: recommendations from the Alzheimer's Association Research Roundtable Workgroup.

机译:淀粉样蛋白修饰治疗试验中与淀粉样蛋白相关的成像异常:阿尔茨海默氏病协会研究圆桌会议的建议。

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摘要

Amyloid imaging related abnormalities (ARIA) have now been reported in clinical trials with multiple therapeutic avenues to lower amyloid-beta burden in Alzheimer's disease (AD). In response to concerns raised by the Food and Drug Administration, the Alzheimer's Association Research Roundtable convened a working group to review the publicly available trial data, attempts at developing animal models, and the literature on the natural history and pathology of related conditions. The spectrum of ARIA includes signal hyperintensities on fluid attenuation inversion recoverysequences thought to represent "vasogenic edema" and/or sulcal effusion (ARIA-E), as well as signal hypointensities on GRE/T2* thought to represent hemosiderin deposits (ARIA-H), including microhemorrhage and superficial siderosis. The etiology of ARIA remains unclear but the prevailing data support vascular amyloid as a common pathophysiological mechanism leading to increased vascular permeability. The workgroup proposes recommendations for the detection and monitoring of ARIA in ongoing AD clinical trials, as well as directions for future research.
机译:现已在临床试验中报道了与淀粉样蛋白成像相关的异常(ARIA),它具有多种治疗途径,可降低阿尔茨海默病(AD)中的淀粉样β负担。为了回应食品药品监督管理局提出的关注,阿尔茨海默氏症协会研究圆桌会议召集了一个工作组,以审查可公开获得的试验数据,开发动物模型的尝试以及有关相关条件的自然史和病理学的文献。 ARIA的频谱包括在流体衰减倒置恢复序列上的信号高强度,被认为代表“血管性水肿”和/或脑腔积液(ARIA-E),以及在GRE / T2 *上的信号低强度,被认为代表血铁蛋白沉积物(ARIA-H)包括微出血和浅表铁症。 ARIA的病因仍不清楚,但主要数据支持血管淀粉样蛋白是导致血管通透性增加的常见病理生理机制。该工作组为正在进行的AD临床试验中ARIA的检测和监测提出了建议,并提出了未来研究的方向。

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