Pawlowski Matthias, Meuth Sven G, Duning Thomas
Department of Neurology, University Hospital Münster, Albert-Schweitzer-Campus 1, Building A1, Münster 48149, Germany.
Diagnostics (Basel). 2017 Jul 13;7(3):42. doi: 10.3390/diagnostics7030042.
Alzheimer's disease is the most common cause of dementia. Over the last three decades, research has advanced dramatically and provided a detailed understanding of the molecular events underlying the pathogenesis of Alzheimer's disease. In parallel, assays for the detection of biomarkers that reflect the typical Alzheimer's disease-associated pathology have been developed and validated in myriads of clinical studies. Such biomarkers complement clinical diagnosis and improve diagnostic accuracy. The use of biomarkers will become even more important with the advent of disease-modifying therapies. Such therapies will likely be most beneficial when administered early in the disease course. Here, we summarise the development of the core Alzheimer's disease cerebrospinal fluid biomarkers: amyloid-β and tau. We provide an overview of their role in cellular physiology and Alzheimer's disease pathology, and embed their development as cerebrospinal fluid biomarkers into the historical context of Alzheimer's disease research. Finally, we summarise recommendations for their use in clinical practice, and outline perspectives for novel cerebrospinal fluid candidate biomarkers.
阿尔茨海默病是痴呆最常见的病因。在过去三十年中,研究取得了巨大进展,对阿尔茨海默病发病机制背后的分子事件有了详细了解。与此同时,反映典型阿尔茨海默病相关病理的生物标志物检测方法已在大量临床研究中得到开发和验证。此类生物标志物辅助临床诊断并提高诊断准确性。随着疾病修饰疗法的出现,生物标志物的应用将变得更加重要。此类疗法在疾病进程早期给药可能最为有益。在此,我们总结了阿尔茨海默病核心脑脊液生物标志物:淀粉样蛋白-β和tau的发展历程。我们概述了它们在细胞生理学和阿尔茨海默病病理学中的作用,并将它们作为脑脊液生物标志物的发展置于阿尔茨海默病研究的历史背景中。最后,我们总结了它们在临床实践中的应用建议,并概述了新型脑脊液候选生物标志物的前景。