Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Malmö, Sweden.
Department of Neurology, Skåne University Hospital, Lund, Sweden.
EMBO Mol Med. 2022 Jan 11;14(1):e14408. doi: 10.15252/emmm.202114408. Epub 2021 Dec 3.
Neurodegenerative disorders such as Alzheimer's disease (AD) represent a mounting public health challenge. As these diseases are difficult to diagnose clinically, biomarkers of underlying pathophysiology are playing an ever-increasing role in research, clinical trials, and in the clinical work-up of patients. Though cerebrospinal fluid (CSF) and positron emission tomography (PET)-based measures are available, their use is not widespread due to limitations, including high costs and perceived invasiveness. As a result of rapid advances in the development of ultra-sensitive assays, the levels of pathological brain- and AD-related proteins can now be measured in blood, with recent work showing promising results. Plasma P-tau appears to be the best candidate marker during symptomatic AD (i.e., prodromal AD and AD dementia) and preclinical AD when combined with Aβ42/Aβ40. Though not AD-specific, blood NfL appears promising for the detection of neurodegeneration and could potentially be used to detect the effects of disease-modifying therapies. This review provides an overview of the progress achieved thus far using AD blood-based biomarkers, highlighting key areas of application and unmet challenges.
神经退行性疾病,如阿尔茨海默病(AD),是当前公共健康面临的严峻挑战。由于这些疾病在临床上难以诊断,因此潜在病理生理学的生物标志物在研究、临床试验和患者的临床评估中发挥着越来越重要的作用。虽然脑脊液(CSF)和正电子发射断层扫描(PET)等检测方法已被应用,但由于成本高、侵入性强等局限性,其应用并不广泛。由于超敏检测方法的快速发展,现在可以在血液中测量病理性脑和 AD 相关蛋白的水平,最近的研究结果表明这是一种很有前景的方法。在有症状 AD(即前驱 AD 和 AD 痴呆)和临床前 AD 中,与 Aβ42/Aβ40 联合检测时,血浆 P-tau 似乎是最佳候选标志物。虽然血液 NfL 不是 AD 特异性的,但它在检测神经退行性变方面很有前景,有可能用于检测疾病修饰疗法的效果。本文综述了迄今为止利用 AD 血液生物标志物取得的进展,重点介绍了关键的应用领域和尚未解决的挑战。