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Biomarkers for the clinical evaluation of the cognitively impaired elderly: Amyloid is not enough

机译:用于认知障碍老年人临床评估的生物标志物:淀粉样蛋白还不够

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The number of elderly patients seeking clinical treatment for memory problems will rise sharply in coming years as our population ages. These patients present a challenge for diagnosis and prognosis since cognitive problems in older patients can arise from many etiologies, some of which are curable. With the development of clinically available biomarkers for detecting Alzheimers disease pathology in living patients, evaluation of cognitively impaired elderly patients is about to undergo a major paradigm shift. This article describes the two classes of biomarkers available for assessing Alzheimers disease risk: those that indicate presence of amyloid pathology and those that provide evidence of neuronal injury and neurodegeneration. We argue that, currently, incorporation of biomarkers of neurodegeneration can help in patient prognosis whereas tests for amyloid, if used in isolation, have potential for harm. Amyloid tests are clinically useful only when evidence suggests progressive cognitive decline or neurodegeneration.
机译:随着我们的人口老龄化,在未来几年中寻求临床治疗记忆问题的老年患者人数将急剧增加。这些患者对诊断和预后提出了挑战,因为老年患者的认知问题可能源于许多病因,其中一些是可以治愈的。随着临床上可用于检测活体患者阿尔茨海默氏病病理的生物标记物的发展,对认知障碍老年患者的评估即将发生重大的范例转变。本文介绍了可用于评估阿尔茨海默氏病风险的两类生物标志物:指示存在淀粉样蛋白病理的生物标志物和提供神经元损伤和神经变性证据的生物标志物。我们认为,目前,掺入神经退行性生物标志物可以帮助患者预后,而淀粉样蛋白的检测(如果单独使用)可能会造成伤害。仅当证据表明进行性认知功能减退或神经退行性变时,淀粉样蛋白测试才在临床上有用。

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