Paraskevaidi Maria, Allsop David, Karim Salman, Martin Francis L, Crean StJohn
School of Pharmacy and Biomedical Sciences, University of Central Lancashire, Preston PR1 2HE, UK.
Department of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London W12 0NN, UK.
J Clin Med. 2020 Jun 1;9(6):1673. doi: 10.3390/jcm9061673.
Studies in the field of Alzheimer's disease (AD) have shown the emergence of biomarkers in biologic fluids that hold great promise for the diagnosis of the disease. A diagnosis of AD at a presymptomatic or early stage may be the key for a successful treatment, with clinical trials currently investigating this. It is anticipated that preventative and therapeutic strategies may be stage-dependent, which means that they have a better chance of success at a very early stage-before critical neurons are lost. Several studies have been investigating the use of cerebrospinal fluid (CSF) and blood as clinical samples for the detection of AD with a number of established core markers, such as amyloid beta (Aβ), total tau (T-tau) and phosphorylated tau (tau), being at the center of clinical research interest. The use of oral samples-including saliva and buccal mucosal cells-falls under one of the least-investigated areas in AD diagnosis. Such samples have great potential to provide a completely non-invasive alternative to current CSF and blood sampling procedures. The present work is a thorough review of the results and analytical approaches, including proteomics, metabolomics, spectroscopy and microbiome analyses that have been used for the study and detection of AD using salivary samples and buccal cells. With a few exceptions, most of the studies utilizing oral samples were performed in small cohorts, which in combination with the existence of contradictory results render it difficult to come to a definitive conclusion on the value of oral markers. Proteins such as Aβ, T-tau and tau, as well as small metabolites, were detected in saliva and have shown some potential as future AD diagnostics. Future large-cohort studies and standardization of sample preparation and (pre-)analytical factors are necessary to determine the use of these non-invasive samples as a diagnostic tool for AD.
阿尔茨海默病(AD)领域的研究表明,生物体液中出现了对该疾病诊断具有巨大潜力的生物标志物。在症状前或早期阶段诊断AD可能是成功治疗的关键,目前临床试验正在对此进行研究。预计预防和治疗策略可能因阶段而异,这意味着在非常早期阶段——在关键神经元丧失之前——它们有更大的成功机会。一些研究一直在调查使用脑脊液(CSF)和血液作为临床样本,以检测AD,一些已确立的核心标志物,如β淀粉样蛋白(Aβ)、总tau蛋白(T-tau)和磷酸化tau蛋白(tau),是临床研究兴趣的核心。使用口腔样本——包括唾液和颊黏膜细胞——属于AD诊断中研究最少的领域之一。此类样本极有可能为当前的脑脊液和血液采样程序提供一种完全非侵入性的替代方法。本研究全面综述了使用唾液样本和颊细胞进行AD研究和检测的结果及分析方法,包括蛋白质组学、代谢组学、光谱学和微生物组分析。除了少数例外,大多数利用口腔样本的研究是在小队列中进行的,再加上结果相互矛盾,因此很难就口腔标志物的价值得出明确结论。唾液中检测到了诸如Aβ、T-tau和tau等蛋白质以及小分子代谢物,它们已显示出作为未来AD诊断标志物的一些潜力。未来需要进行大规模队列研究以及样本制备和(预)分析因素的标准化,以确定这些非侵入性样本作为AD诊断工具的用途。