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神经血管单元作为缺血性脑卒中生物标志物的来源——实验研究的局限性及临床应用展望。

Neurovascular Unit as a Source of Ischemic Stroke Biomarkers-Limitations of Experimental Studies and Perspectives for Clinical Application.

机构信息

Faculty of Health Sciences, Pomeranian University of Slupsk, 64 Bohaterów Westerplatte St., 76-200, Slupsk, Poland.

Department of Anatomy and Neurobiology, Medical University of Gdansk, 1 Debinki St., 80-211, Gdansk, Poland.

出版信息

Transl Stroke Res. 2020 Aug;11(4):553-579. doi: 10.1007/s12975-019-00744-5. Epub 2019 Nov 7.

DOI:10.1007/s12975-019-00744-5
PMID:31701356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7340668/
Abstract

Cerebral stroke, which is one of the most frequent causes of mortality and leading cause of disability in developed countries, often leads to devastating and irreversible brain damage. Neurological and neuroradiological diagnosis of stroke, especially in its acute phase, is frequently uncertain or inconclusive. This results in difficulties in identification of patients with poor prognosis or being at high risk for complications. It also makes difficult identification of these stroke patients who could benefit from more aggressive therapies. In contrary to the cardiovascular disease, no single biomarker is available for the ischemic stroke, addressing the abovementioned issues. This justifies the need for identifying of effective diagnostic measures characterized by high specificity and sensitivity. One of the promising avenues in this area is studies on the panels of biomarkers characteristic for processes which occur in different types and phases of ischemic stroke and represent all morphological constituents of the brains' neurovascular unit (NVU). In this review, we present the current state of knowledge concerning already-used or potentially applicable biomarkers of the ischemic stroke. We also discuss the perspectives for identification of biomarkers representative for different types and phases of the ischemic stroke, as well as for different constituents of NVU, which concentration levels correlate with extent of brain damage and patients' neurological status. Finally, a critical analysis of perspectives on further improvement of the ischemic stroke diagnosis is presented.

摘要

脑卒中是发达国家最常见的死亡原因之一,也是导致残疾的主要原因,常导致毁灭性和不可逆转的脑损伤。脑卒中的神经和神经放射学诊断,尤其是在其急性期,往往不确定或不确定。这导致难以识别预后不良或有并发症高风险的患者。也难以识别那些可能受益于更积极治疗的脑卒中患者。与心血管疾病不同,缺血性脑卒中没有单一的生物标志物可以解决上述问题。这证明需要确定具有高特异性和敏感性的有效诊断措施。在这方面有希望的途径之一是研究在不同类型和阶段的缺血性脑卒中发生的过程中具有特征的生物标志物,代表大脑神经血管单元 (NVU) 的所有形态成分。在这篇综述中,我们介绍了目前关于已经使用或潜在适用的缺血性脑卒中生物标志物的知识状况。我们还讨论了鉴定代表缺血性脑卒中不同类型和阶段以及 NVU 不同成分的生物标志物的前景,这些标志物的浓度水平与脑损伤程度和患者的神经状态相关。最后,对进一步改善缺血性脑卒中诊断的前景进行了批判性分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce74/7340668/8edf6dae2bd5/12975_2019_744_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce74/7340668/9dc72d8dccec/12975_2019_744_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce74/7340668/8edf6dae2bd5/12975_2019_744_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce74/7340668/9dc72d8dccec/12975_2019_744_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce74/7340668/8edf6dae2bd5/12975_2019_744_Fig2_HTML.jpg

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本文引用的文献

1
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Front Cell Neurosci. 2019 Mar 7;13:77. doi: 10.3389/fncel.2019.00077. eCollection 2019.
2
Amino Acid Biosignature in Plasma among Ischemic Stroke Subtypes.血浆中氨基酸生物标志物与缺血性脑卒中亚型。
Biomed Res Int. 2019 Jan 20;2019:8480468. doi: 10.1155/2019/8480468. eCollection 2019.
3
Involvement of classical neurotransmitter systems in memory reconsolidation: Focus on destabilization.经典神经递质系统在记忆再巩固中的作用:聚焦于去稳定化。
脑病中的神经血管耦合功能障碍:病理生理学进展及临床意义
Front Neurol. 2025 May 20;16:1522485. doi: 10.3389/fneur.2025.1522485. eCollection 2025.
4
Assessment of Phase-Dependent Alterations in Cortical Glycolytic and Mitochondrial Metabolism Following Ischemic Stroke.缺血性中风后皮质糖酵解和线粒体代谢的相位依赖性改变评估
ASN Neuro. 2025;17(1):2488935. doi: 10.1080/17590914.2025.2488935. Epub 2025 Apr 10.
5
Blood Biomarkers in Ischemic Stroke Diagnostics and Treatment-Future Perspectives.缺血性中风诊断与治疗中的血液生物标志物——未来展望
Medicina (Kaunas). 2025 Mar 17;61(3):514. doi: 10.3390/medicina61030514.
6
Advances in the detection of biomarkers for ischemic stroke.缺血性中风生物标志物检测的进展
Front Neurol. 2025 Feb 24;16:1488726. doi: 10.3389/fneur.2025.1488726. eCollection 2025.
7
A review of the 's intervention mechanism and clinical application in ischemic stroke.关于“[具体干预措施]”在缺血性卒中中的干预机制及临床应用的综述。 (注:原文中‘’处内容缺失,需补充完整具体的干预措施名称才能准确翻译)
Front Pharmacol. 2025 Jan 15;15:1510779. doi: 10.3389/fphar.2024.1510779. eCollection 2024.
8
GFAP as Astrocyte-Derived Extracellular Vesicle Cargo in Acute Ischemic Stroke Patients-A Pilot Study.胶质纤维酸性蛋白作为急性缺血性脑卒中患者星形细胞衍生细胞外囊泡的载体:一项初步研究。
Int J Mol Sci. 2024 May 24;25(11):5726. doi: 10.3390/ijms25115726.
9
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Biophys Rev. 2023 Sep 4;15(5):1279-1286. doi: 10.1007/s12551-023-01121-1. eCollection 2023 Oct.
10
Brain pericyte biology: from physiopathological mechanisms to potential therapeutic applications in ischemic stroke.脑周细胞生物学:从病理生理机制到缺血性卒中的潜在治疗应用
Front Cell Neurosci. 2023 Sep 14;17:1267785. doi: 10.3389/fncel.2023.1267785. eCollection 2023.
Neurobiol Learn Mem. 2018 Dec;156:68-79. doi: 10.1016/j.nlm.2018.11.001. Epub 2018 Nov 2.
4
Clinical and laboratory factors related to acute isolated vertigo or dizziness and cerebral infarction.与急性孤立性眩晕或头晕和脑梗死相关的临床和实验室因素。
Brain Behav. 2018 Sep;8(9):e01092. doi: 10.1002/brb3.1092. Epub 2018 Aug 11.
5
Association between matrix metalloproteinase family gene polymorphisms and risk of ischemic stroke: A systematic review and meta-analysis of 29 studies.基质金属蛋白酶家族基因多态性与缺血性脑卒中风险的关联:29 项研究的系统评价和荟萃分析。
Gene. 2018 Sep 25;672:180-194. doi: 10.1016/j.gene.2018.06.027. Epub 2018 Jun 12.
6
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J Korean Neurosurg Soc. 2018 Sep;61(5):548-558. doi: 10.3340/jkns.2017.0200. Epub 2018 May 4.
7
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Mol Med Rep. 2018 Jun;17(6):8196-8202. doi: 10.3892/mmr.2018.8888. Epub 2018 Apr 16.
8
Blood biomarkers in ischemic stroke: potential role and challenges in clinical practice and research.缺血性脑卒中的血液生物标志物:在临床实践和研究中的潜在作用和挑战。
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9
Inhibition in the amygdala anxiety circuitry.杏仁核焦虑回路的抑制。
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10
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