Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Boston, MA, USA; Department of Neurology, Harvard Medical School, Boston, MA, USA.
Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden; Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden; Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, UK; UK Dementia Research Institute at UCL, London, UK; Hong Kong Center for Neurodegenerative Diseases, Hong Kong, China.
J Neurosci Methods. 2021 Sep 1;361:109281. doi: 10.1016/j.jneumeth.2021.109281. Epub 2021 Jul 6.
Neurodegenerative diseases are heterogeneous in their cause and clinical presentation making clinical assessment and disease monitoring challenging. Because of this, there is an urgent need for objective tools such as fluid biomarkers able to quantitate different aspects of the disease. In the last decade, technological improvements and awareness of the importance of biorepositories led to the discovery of an evolving number of fluid biomarkers covering the main characteristics of neurodegenerative diseases such as neurodegeneration, protein aggregates and inflammation. The ability to quantitate each aspect of the disease at a high definition enables a more precise stratification of the patients at inclusion in clinical trials, hence reducing the noise that may hamper the detection of therapeutical efficacy and allowing for smaller but likewise powered studies, which particularly improves the ability to start clinical trials for rare neurological diseases. Moreover, the use of fluid biomarkers has the potential to support a targeted therapeutical intervention, as it is now emerging for the treatment of amyloid-beta deposition in patients suffering from Alzheimer's disease. Here we review the knowledge that evolved from the measurement of fluid biomarker proteins in neurodegenerative conditions.
神经退行性疾病在病因和临床表现上存在异质性,这使得临床评估和疾病监测具有挑战性。因此,迫切需要一些客观的工具,如能够定量评估疾病不同方面的体液生物标志物。在过去的十年中,技术的进步和对生物库重要性的认识,促使人们发现了越来越多的能够涵盖神经退行性疾病主要特征的体液生物标志物,如神经退行性变、蛋白质聚集和炎症。能够以高清晰度定量评估疾病的各个方面,使得在临床试验纳入患者时能够进行更精确的分层,从而减少可能阻碍治疗效果检测的噪声,并允许进行更小但同样有力的研究,这尤其提高了开展罕见神经疾病临床试验的能力。此外,体液生物标志物的使用有可能支持靶向治疗干预,因为现在已经开始在治疗阿尔茨海默病患者的淀粉样β沉积方面应用。在这里,我们回顾了在神经退行性疾病中测量体液生物标志物蛋白所获得的知识。