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Perspective: Clinical relevance of the dichotomous classification of Alzheimer's disease biomarkers: Should there be a “gray zone”?

机译:透视:阿尔茨海默病生物标志物二分法分类的临床相关性:应该有一个“灰色区域”吗?

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摘要

Abstract The 2018 National Institute on Aging and the Alzheimer's Association (NIA‐AA) research framework recently redefined Alzheimer's disease (AD) as a biological construct, based on in?vivo biomarkers reflecting key neuropathologic features. Combinations of normal/abnormal levels of three biomarker categories, based on single thresholds, form the AD signature profile that defines the biological disease state as a continuum, independent of clinical symptomatology. While single thresholds may be useful in defining the biological signature profile, we provide evidence that their use in studies with cognitive outcomes merits further consideration. Using data from the Alzheimer's Disease Neuroimaging Initiative with a focus on cortical amyloid binding, we discuss the limitations of applying the biological definition of disease status as a tool to define the increased likelihood of the onset of the Alzheimer's clinical syndrome and the effects that this may have on trial study design. We also suggest potential research objectives going forward and what the related data requirements would be.
机译:摘要2018年老龄化学院和阿尔茨海默氏症协会(NIA-AA)研究框架最近重新定义了阿尔茨海默病(AD)作为一种生物结构,基于反映关键神经病理学特征的体内生物标志物。基于单个阈值的三个生物标志物类别的正常/异常水平的组合形成了将生物疾病状态定义为连续体,与临床症状学相同的广告签名轮廓。虽然单个阈值可能有用在定义生物签名简介中,但我们提供了证据表明他们在认知结果的研究中使用了优异的考虑。使用来自阿尔茨海默病的疾病的数据具有重点在皮质淀粉样蛋白结合的关注,我们讨论了将疾病状态的生物学定义作为一种临床综合征起发作增加的疾病的生物学定义以及这可能有试验研究设计。我们还建议潜在的研究目标,以及相关数据要求是什么。

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