Mohamed Bouftas, 610 Purdue Mall, West Lafayette, IN 47907, USA,
J Prev Alzheimers Dis. 2021;8(1):84-91. doi: 10.14283/jpad.2020.57.
Early AD diagnosis is critical for ameliorating prognosis and treatment. The analysis of CSF biomarkers yields accurate results, but it necessitates a lumbar puncture procedure. Screening for peripheral biomarkers in saliva is advantageous since this medium is noninvasive and inexpensive to obtain. The objective of this systematic review is to analyze saliva biomarker studies which aim to diagnose AD. Titles, abstracts, and reference lists for publications from January 2004 to February 2020 were screened for by searching Google Scholar and PubMed. The inclusion criteria involved published studies that consisted of both AD and control groups. 88 studies were screened, and 20 publications fulfilled the inclusion criteria. These selected publications were scrutinized and included in this review. Aβ42, tau, certain metabolites, and oral microbiota might serve as reliable biomarkers for AD diagnosis. These results showcase the legitimate feasibility of proteomic, metabolomic, and microbiotic compounds in saliva for AD diagnostics in the near future. Supplemental studies must consider standardizing the analytical methods of measuring salivary biomarkers to establish coherence for the selection of valid AD biomarkers. Validation studies will require a large sample size of biomarker-diagnosed individuals for independent populations. This ensures accuracy and rigidity for receiver operating characteristic (ROC) curves that can be set for the most optimal salivary biomarkers in future clinical settings.
早期诊断对于改善预后和治疗至关重要。分析脑脊液生物标志物可得出准确的结果,但需要进行腰椎穿刺。筛选唾液中的外周生物标志物具有优势,因为这种介质是非侵入性的,并且获取成本低廉。本系统综述的目的是分析旨在诊断 AD 的唾液生物标志物研究。通过在 Google Scholar 和 PubMed 上搜索,筛选了 2004 年 1 月至 2020 年 2 月发表的出版物的标题、摘要和参考文献列表。纳入标准包括包含 AD 和对照组的发表研究。共筛选了 88 项研究,有 20 篇出版物符合纳入标准。对这些选定的出版物进行了仔细审查,并纳入了本综述。Aβ42、tau、某些代谢物和口腔微生物群可能成为 AD 诊断的可靠生物标志物。这些结果展示了在不久的将来,唾液中的蛋白质组学、代谢组学和微生物组学化合物在 AD 诊断中的合法可行性。补充研究必须考虑标准化测量唾液生物标志物的分析方法,以建立用于选择有效 AD 生物标志物的一致性。验证研究需要具有生物标志物诊断个体的大样本量,用于独立人群。这确保了未来临床环境中最佳唾液生物标志物的接收者操作特征 (ROC) 曲线的准确性和严格性。