呼吁改善临床和认知评估,以减少淀粉样蛋白/Tau病理发病与认知功能障碍检测之间的差距。

Jordi A Matias-Guiu, Rosie E Curiel-Cid, Bruce P Hermann, David A Loewenstein
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引用次数: 0

摘要

在这篇评论中,我们讨论了关于阿尔茨海默病的定义和标准的新观点,特别是与生物学和临床生物学方法有关的观点。我们认为,研究必须继续专注于改进临床和认知工具,以将生物标志物发现置于背景中,并在个体水平上理解不同病理生理过程的临床意义。我们提出了几种解决方案,包括开发“认知压力测试”、数字临床生物标志物、创新的分析程序、更精细的研究以收集严格和纵向的规范数据,以及最终提高临床技能。总的来说,这些策略可以帮助“缩短”临床前时间,并通过更有效地将生物标志物异常与认知功能障碍的发病联系起来,弥合生物学和临床生物学方法之间的差距。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Call for Improving Clinical and Cognitive Assessments to Reduce the Gap Between Amyloid/Tau Pathology Onset and Detection of Cognitive Dysfunction.

In this commentary, we discuss the new perspectives on the definition and criteria for Alzheimer's disease, particularly in relation to the biological and clinical-biological approaches. We argue that research must continue to focus on improving clinical and cognitive tools to contextualize biomarker findings and understand the clinical implications of different pathophysiological processes at the individual level. We propose several solutions, including the development of "cognitive stress tests," digital clinical biomarkers, innovative analytical procedures, more refined studies for collecting rigorous and longitudinal normative data, and, ultimately, enhanced clinical skills. Overall, these strategies could help "shorten" the preclinical period and bridge the gap between the biological and clinical-biological approaches by aligning biomarker abnormalities with the onset of cognitive dysfunction more effectively.

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