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用于阿尔茨海默病诊断和进展的基于血液的生物标志物:概述。

Blood-Based Biomarkers for Alzheimer's Disease Diagnosis and Progression: An Overview.

机构信息

Department of Biology and Biotechnology, University of Pavia, 27100 Pavia, Italy.

Almo Collegio Borromeo, 27100 Pavia, Italy.

出版信息

Cells. 2022 Apr 17;11(8):1367. doi: 10.3390/cells11081367.

Abstract

Alzheimer's Disease (AD) is a progressive neurodegenerative disease characterized by amyloid-β (Aβ) plaque deposition and neurofibrillary tangle accumulation in the brain. Although several studies have been conducted to unravel the complex and interconnected pathophysiology of AD, clinical trial failure rates have been high, and no disease-modifying therapies are presently available. Fluid biomarker discovery for AD is a rapidly expanding field of research aimed at anticipating disease diagnosis and following disease progression over time. Currently, Aβ, phosphorylated tau, and total tau levels in the cerebrospinal fluid are the best-studied fluid biomarkers for AD, but the need for novel, cheap, less-invasive, easily detectable, and more-accessible markers has recently led to the search for new blood-based molecules. However, despite considerable research activity, a comprehensive and up-to-date overview of the main blood-based biomarker candidates is still lacking. In this narrative review, we discuss the role of proteins, lipids, metabolites, oxidative-stress-related molecules, and cytokines as possible disease biomarkers. Furthermore, we highlight the potential of the emerging miRNAs and long non-coding RNAs (lncRNAs) as diagnostic tools, and we briefly present the role of vitamins and gut-microbiome-related molecules as novel candidates for AD detection and monitoring, thus offering new insights into the diagnosis and progression of this devastating disease.

摘要

阿尔茨海默病(AD)是一种进行性神经退行性疾病,其特征是大脑中淀粉样蛋白-β(Aβ)斑块沉积和神经纤维缠结积聚。尽管已经进行了几项研究来揭示 AD 的复杂和相互关联的病理生理学,但临床试验失败率一直很高,目前尚无疾病修饰疗法。AD 的液体检标志发现是一个快速发展的研究领域,旨在预测疾病诊断,并随着时间的推移跟踪疾病进展。目前,脑脊液中 Aβ、磷酸化 tau 和总 tau 水平是研究最充分的 AD 液体检标志,但需要新的、廉价的、创伤性更小的、更易检测的和更容易获得的标志物,最近导致了对新的基于血液的分子的探索。然而,尽管研究活动相当多,但仍缺乏对主要基于血液的生物标志物候选物的全面和最新概述。在这篇叙述性综述中,我们讨论了蛋白质、脂质、代谢物、氧化应激相关分子和细胞因子作为可能的疾病生物标志物的作用。此外,我们强调了新兴的 microRNA 和长非编码 RNA(lncRNA)作为诊断工具的潜力,并简要介绍了维生素和肠道微生物群相关分子作为 AD 检测和监测的新候选物的作用,从而为这种破坏性疾病的诊断和进展提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f7c/9044750/07feabf84c16/cells-11-01367-g001.jpg

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