Kodosaki Eleftheria, Zetterberg Henrik, Heslegrave Amanda
Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK.
Dementia Research Institute at UCL, London, UK.
Expert Rev Mol Diagn. 2023 Jul-Dec;23(12):1153-1165. doi: 10.1080/14737159.2023.2289553. Epub 2023 Dec 15.
In recent years, exciting developments in disease modifying treatments for Alzheimer's disease (AD) have made accurate and timely diagnosis of this disease a priority. Blood biomarkers (BBMs) for amyloid pathology using improved immunoassay and mass spectrometry techniques have been an area of intense research for the last 10 years and are coming to the fore, as a real prospect to be used in the clinical diagnostics of the disease.
The following review will update and discuss blood biomarkers that will be most useful in diagnosing AD and the context necessary for their implementation.
It is clear we now have BBMs, and technology to measure them, that are capable of detecting amyloid pathology in AD. The challenge is to validate them across platforms and populations to incorporate them into clinical practice. It is important that implementation comes with education, we need to give clinicians the tools for appropriate use and interpretation. It is feasible that BBMs will be used to screen populations, initially for clinical trial entry but also therapeutic intervention in the foreseeable future. We now need to focus BBM research on other pathologies to ensure we accelerate the development of therapeutics for all neurodegenerative diseases.
近年来,阿尔茨海默病(AD)疾病修饰治疗方面令人兴奋的进展使该疾病的准确及时诊断成为当务之急。在过去10年中,利用改进的免疫测定和质谱技术检测淀粉样蛋白病理的血液生物标志物(BBM)一直是深入研究的领域,并且作为一种可用于该疾病临床诊断的切实可行的方法正崭露头角。
以下综述将更新并讨论在AD诊断中最有用的血液生物标志物及其应用所需的背景知识。
显然,我们现在拥有能够检测AD中淀粉样蛋白病理的BBM及其测量技术。挑战在于在不同平台和人群中对它们进行验证,以便将其纳入临床实践。实施过程中开展教育很重要,我们需要为临床医生提供正确使用和解读的工具。BBM用于人群筛查是可行的,最初用于临床试验入组,在可预见的未来也可用于治疗干预。我们现在需要将BBM研究重点放在其他病理方面,以确保加速所有神经退行性疾病治疗方法的开发。