阿尔茨海默病诊断的新景观

Giovanni B Frisoni, Oskar Hansson, Emma Nichols, Valentina Garibotto, Suzanne E Schindler, Wiesje M van der Flier, Frank Jessen, Nicolas Villain, Eider M Arenaza-Urquijo, Lucia Crivelli, Juan Fortea, Lea T Grinberg, Zahinoor Ismail, Satoshi Minoshima, Rik Ossenkoppele, Henrik Zetterberg, Ronald C Petersen, Bruno Dubois
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引用次数: 0

摘要

阿尔茨海默病严重偏离了正常衰老的认知、功能和行为轨迹,是一种可怕的、非常普遍的个人残疾原因,也是社会卫生和社会护理支出的主要来源。在生物标志物出现之前,死后检查是唯一可用于确定诊断的方法。在该系列的第一篇论文中,我们回顾了最先进的诊断实践和专家设置的典型患者旅程,临床医生参与鉴别诊断,以确定阿尔茨海默病的病理(β-淀粉样蛋白和过度磷酸化的tau沉积)是否是认知障碍的一个贡献者。表明β-淀粉样蛋白和tau稳态失调的生物标志物,用PET和脑脊液分析测量,允许分子水平的诊断-这是确定最近批准的抗淀粉样蛋白治疗资格的强制性步骤。我们预计,一些国家已经提供的易于获得的血液生物标志物将导致一场新的诊断革命,并给全世界的卫生保健系统带来重大变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New landscape of the diagnosis of Alzheimer's disease
Alzheimer's disease involves a drastic departure from the cognitive, functional, and behavioural trajectory of normal ageing, and is both a dreaded and highly prevalent cause of disability to individuals, and a leading source of health and social care expenditure for society. Before the advent of biomarkers, post-mortem examination was the only method available to establish a definitive diagnosis. In this first paper of the Series, we review state-of-the-art diagnostic practices and the typical patient journey in specialist settings, where clinicians engage in a differential diagnosis to establish whether Alzheimer's pathology (cerebral deposition of β-amyloid and hyperphosphorylated tau) is a contributor to cognitive impairment. Biomarkers indicating dysregulation of β-amyloid and tau homeostasis, measured with PET and cerebrospinal fluid analysis, allow a molecular-level diagnosis—a mandatory step in defining eligibility for the recently approved anti-amyloid treatments. We anticipate that easily accessible blood biomarkers, already available in some countries, will lead to a new diagnostic revolution and bring about major changes in health-care systems worldwide.
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