AXA Research Fund and Sorbonne University Chair, Paris, France.
Sorbonne University, GRC n° 21, Alzheimer Precision Medicine (APM), AP-HP, Pitié-Salpêtrière Hospital, Paris, France.
Nat Rev Neurol. 2018 Nov;14(11):639-652. doi: 10.1038/s41582-018-0079-7.
Biomarker discovery and development for clinical research, diagnostics and therapy monitoring in clinical trials have advanced rapidly in key areas of medicine - most notably, oncology and cardiovascular diseases - allowing rapid early detection and supporting the evolution of biomarker-guided, precision-medicine-based targeted therapies. In Alzheimer disease (AD), breakthroughs in biomarker identification and validation include cerebrospinal fluid and PET markers of amyloid-β and tau proteins, which are highly accurate in detecting the presence of AD-associated pathophysiological and neuropathological changes. However, the high cost, insufficient accessibility and/or invasiveness of these assays limit their use as viable first-line tools for detecting patterns of pathophysiology. Therefore, a multistage, tiered approach is needed, prioritizing development of an initial screen to exclude from these tests the high numbers of people with cognitive deficits who do not demonstrate evidence of underlying AD pathophysiology. This Review summarizes the efforts of an international working group that aimed to survey the current landscape of blood-based AD biomarkers and outlines operational steps for an effective academic-industry co-development pathway from identification and assay development to validation for clinical use.
生物标志物在临床研究、临床试验中的诊断和治疗监测中的发现和开发在医学的关键领域迅速发展——在肿瘤学和心血管疾病方面尤为显著——使早期快速检测成为可能,并支持了基于生物标志物指导的、精准医学为基础的靶向治疗的发展。在阿尔茨海默病(AD)中,生物标志物鉴定和验证方面的突破包括脑脊液和淀粉样蛋白-β和tau 蛋白的 PET 标志物,这些标志物在检测 AD 相关病理生理和神经病理学变化的存在方面具有高度准确性。然而,这些检测的高成本、不足的可及性和/或侵入性限制了它们作为检测病理生理学模式的可行一线工具的使用。因此,需要采用多阶段、分层的方法,优先开发初始筛选,以排除这些测试中大量认知障碍但没有表现出潜在 AD 病理生理学证据的人群。这篇综述总结了一个国际工作组的努力,该工作组旨在调查基于血液的 AD 生物标志物的现状,并概述了从鉴定和检测开发到临床应用验证的有效学术-产业共同开发途径的操作步骤。