Molecular Markers Laboratory, IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Brescia, Italy.
Don Carlo Gnocchi ONLUS Foundation, Milan, Italy.
J Alzheimers Dis. 2018;62(4):1507-1518. doi: 10.3233/JAD-170953.
The criteria for the clinical diagnosis of AD include the analysis of biomarkers of the underlying brain disease pathology; a set of cerebrospinal fluid (CSF) tests, amyloid-β1-42 (Aβ42), total-tau (t-tau), and phosphorylated tau (p-tau), are available and their performance in a clinical setting has been assessed in several studies. Thus, in dementia research, great advances have been made in the discovery of putative biomarkers; however, disappointingly, few of them have been translated into clinically applicable assays. To find biomarkers able to reliably detect AD pathology already at prodromal stages and in blood is even more important. Recent technical breakthroughs have provided ultrasensitive methods that allow the detection of brain-specific proteins in blood. In the present review, we will focus on the usefulness of ultrasensitive technologies for biomarker discovery and trace elements detection; moreover, we will review studies on circulating nano-compartments, a promising novel source of material for molecular diagnostics.
AD 的临床诊断标准包括对潜在脑疾病病理的生物标志物进行分析;有一套脑脊液 (CSF) 测试,包括淀粉样蛋白-β1-42 (Aβ42)、总 tau (t-tau) 和磷酸化 tau (p-tau),已经在多项研究中评估了其在临床环境中的性能。因此,在痴呆症研究中,在发现潜在生物标志物方面取得了重大进展;然而,令人失望的是,其中很少有转化为临床应用的检测方法。发现能够在疾病前驱期可靠地检测 AD 病理的生物标志物,甚至在血液中检测,更为重要。最近的技术突破提供了超灵敏的方法,可以在血液中检测到大脑特异性蛋白质。在本综述中,我们将重点介绍超灵敏技术在生物标志物发现和微量元素检测中的应用;此外,我们还将回顾循环纳米隔间的研究,这是一种有前途的分子诊断新物质来源。