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中风的液体生物标志物:从动物模型到临床护理。

Fluid biomarkers in stroke: From animal models to clinical care.

机构信息

Department of Neurology, Centro Hospitalar Universitário do Porto, Porto, Portugal.

i3S - Instituto de Investigação e Inovação em Saúde, University of Porto, Porto, Portugal.

出版信息

Acta Neurol Scand. 2022 Oct;146(4):332-347. doi: 10.1111/ane.13668. Epub 2022 Jul 15.

Abstract

Stroke is a leading cause of death and disability worldwide. Stroke prevention, early diagnosis, and efficient acute treatment are priorities to successfully impact stroke death and disability. Fluid biomarkers may improve stroke differential diagnostic, patient stratification for acute treatment, and post-stroke individualized rehabilitation. In the present work, we characterized the use of stroke animal models in fluid biomarker research through a systematic review of PubMed and Scopus databases, followed by a literature review on the translation to the human stroke care setting and future perspectives in the field. We found increasing numbers of publications but with limited translation to the clinic. Animal studies are very heterogeneous, do not account for several human features present in stroke, and, importantly, only a minority of such studies used human cohorts to validate biomarker findings. Clinical studies have found appealing candidates, both protein and circulating nucleic acids, to contribute to a more personalized stroke care pathway. Still, brain tissue complexity and the fact that different brain pathologies share lesion biomarkers make this task challenging due to biomarker low specificity. Moreover, the study design and lack of validation cohorts may have precluded a formal integration of biomarkers in different steps of stroke diagnosis and treatment. To overcome such issues, recent pivotal studies on biomarker dynamics in individual patients are providing added value to diagnosis and anticipating patients' early prognosis. Presently, the most consistent protein biomarkers for stroke diagnosis and short- and long-term prognosis are associated with tissue damage at neuronal (TAU), axonal (NFL), or astroglial (GFAP and S100β) levels. Most promising nucleic acids are microRNAs (miR), due to their stability in plasma and ease of access. Still, clinical validation and standardized quantitation place them a step behind compared protein as stroke biomarkers. Ultimately, the definition of clinically relevant biomarker panels and optimization of fast and sensitive biomarker measurements in the blood, together with their combination with clinical and neuroimaging data, will pave the way toward personalized stroke care.

摘要

中风是全球范围内导致死亡和残疾的主要原因。预防中风、早期诊断和有效的急性治疗是成功降低中风死亡率和残疾率的重点。液体生物标志物可以改善中风的鉴别诊断、急性治疗的患者分层以及中风后的个体化康复。在本工作中,我们通过对 PubMed 和 Scopus 数据库进行系统回顾,对液体生物标志物研究中的中风动物模型的使用进行了特征描述,随后对其在人类中风护理环境中的转化以及该领域的未来展望进行了文献回顾。我们发现发表的文献数量在不断增加,但向临床的转化有限。动物研究非常多样化,没有考虑到中风中存在的几种人类特征,而且,重要的是,只有少数此类研究使用人类队列来验证生物标志物的发现。临床研究已经发现了有吸引力的候选物,包括蛋白质和循环核酸,以促进更个性化的中风护理途径。尽管如此,由于生物标志物特异性低,大脑组织的复杂性以及不同的脑病理学共享病变生物标志物,使得这一任务具有挑战性。此外,研究设计和缺乏验证队列可能阻碍了生物标志物在中风诊断和治疗的不同步骤中的正式整合。为了克服这些问题,最近对个体患者中生物标志物动态的重要研究为诊断提供了附加值,并预测了患者的早期预后。目前,用于中风诊断和短期及长期预后的最一致的蛋白质生物标志物与神经元(TAU)、轴突(NFL)或星形胶质细胞(GFAP 和 S100β)水平的组织损伤有关。最有前途的核酸是 microRNAs(miR),因为它们在血浆中稳定且易于获取。尽管如此,与蛋白质相比,它们在临床验证和标准化定量方面仍落后一步。最终,定义临床上相关的生物标志物谱,并优化血液中快速和敏感的生物标志物测量,以及将其与临床和神经影像学数据相结合,将为个性化中风护理铺平道路。

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