Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
GRC N° 21, Alzheimer Precision Medicine (APM), AP-HP, Pitié-Salpêtrière Hospital, Boulevard De L'hôpital, Sorbonne University, Paris, France.
Expert Rev Proteomics. 2021 Jan;18(1):27-48. doi: 10.1080/14789450.2021.1886929. Epub 2021 Mar 7.
: Tau protein misfolding and accumulation in toxic species is a critical pathophysiological process of Alzheimer's disease (AD) and other neurodegenerative disorders (NDDs). Tau biomarkers, namely cerebrospinal fluid (CSF) total-tau (t-tau), 181-phosphorylated tau (p-tau), and tau-PET tracers, have been recently embedded in the diagnostic criteria for AD. Nevertheless, the role of tau as a diagnostic and prognostic biomarker for other NDDs remains controversial.: We performed a systematical PubMed-based review of the most recent advances in tau-related biomarkers for NDDs. We focused on papers published from 2015 to 2020 assessing the diagnostic or prognostic value of each biomarker.: The assessment of tau biomarkers in alternative easily accessible matrices, through the development of ultrasensitive techniques, represents the most significant perspective for AD-biomarker research. In NDDs, novel tau isoforms (e.g. p-tau217) or proteolytic fragments (e.g. N-terminal fragments) may represent candidate diagnostic and prognostic biomarkers and may help monitoring disease progression. Protein misfolding amplification assays, allowing the identification of different tau strains (e.g. 3 R- . 4 R-tau) in CSF, may constitute a breakthrough for the in vivo stratification of NDDs. Tau-PET may help tracking the spatial-temporal evolution of tau pathophysiology in AD but its application outside the AD-spectrum deserves further studies.
tau 蛋白错误折叠和聚集形成毒性物种是阿尔茨海默病(AD)和其他神经退行性疾病(NDD)的关键病理生理过程。tau 生物标志物,即脑脊液(CSF)总 tau(t-tau)、181 位磷酸化 tau(p-tau)和 tau-PET 示踪剂,最近已被纳入 AD 的诊断标准。然而,tau 作为其他 NDD 的诊断和预后生物标志物的作用仍存在争议。
我们基于 PubMed 进行了一项系统性综述,研究了与 NDD 相关的 tau 生物标志物的最新进展。我们重点关注了 2015 年至 2020 年期间发表的评估每种生物标志物诊断或预后价值的论文。
通过开发超灵敏技术,在替代的易于获取的基质中评估 tau 生物标志物,代表了 AD 生物标志物研究的最重要前景。在 NDD 中,新型 tau 同工型(例如 p-tau217)或蛋白水解片段(例如 N 端片段)可能是候选的诊断和预后生物标志物,并有助于监测疾病进展。蛋白错误折叠放大测定法允许在 CSF 中鉴定不同的 tau 株(例如 3R-、4R-tau),这可能是 NDD 体内分层的突破。tau-PET 可能有助于追踪 AD 中 tau 病理生理学的时空演变,但在 AD 谱之外的应用值得进一步研究。