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血浆可溶性尿激酶型纤溶酶原激活物受体与动脉瘤性蛛网膜下腔出血患者的神经功能结局无关。

Plasma Soluble Urokinase-Type Plasminogen Activator Receptor Is Not Associated with Neurological Outcome in Patients with Aneurysmal Subarachnoid Hemorrhage.

作者信息

Kiiski Heikki, Jalkanen Ville, Ala-Peijari Marika, Hämäläinen Mari, Moilanen Eeva, Peltola Jukka, Tenhunen Jyrki

机构信息

Critical Care Medicine Research Group, Department of Intensive Care, Tampere University Hospital, Tampere, Finland.

The Immunopharmacology Research Group, Faculty of Medicine and Life Sciences, University of Tampere, Tampere University Hospital, Tampere, Finland.

出版信息

Front Neurol. 2017 Apr 18;8:144. doi: 10.3389/fneur.2017.00144. eCollection 2017.

DOI:10.3389/fneur.2017.00144
PMID:28458650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5394110/
Abstract

OBJECT

Aneurysmal subarachnoid hemorrhage (aSAH) is a common cause of death or long-term disability. Despite advances in neurocritical care, there is still only a very limited ability to monitor the development of secondary brain injury or to predict neurological outcome after aSAH. Soluble urokinase-type plasminogen activator receptor (suPAR) has shown potential as a prognostic and as an inflammatory biomarker in a wide range of critical illnesses since it displays an association with overall immune system activation. This is the first time that suPAR has been evaluated as a prognostic biomarker in aSAH.

METHODS

In this prospective population-based study, plasma suPAR levels were measured in aSAH patients ( = 47) for up to 5 days. suPAR was measured at 0, 12, and 24 h after patient admission to the intensive care unit (ICU) and daily thereafter until he/she was transferred from the ICU. The patients' neurological outcome was evaluated with the modified Rankin Scale (mRS) at 6 months after aSAH.

RESULTS

suPAR levels ( = 47) during the first 24 h after aSAH were comparable in groups with a favorable (mRS 0-2) or an unfavorable (mRS 3-6) outcome. suPAR levels during the first 24 h were not associated with the findings in the primary brain CT, with acute hydrocephalus, or with antimicrobial medication use during 5-days' follow-up. suPAR levels were associated with generally accepted inflammatory biomarkers (C-reactive protein, leukocyte count).

CONCLUSION

Plasma suPAR level was not associated with either neurological outcome or selected clinical conditions. While suPAR is a promising biomarker for prognostication in several conditions requiring intensive care, it did not reveal any value as a prognostic biomarker after aSAH.

摘要

目的

动脉瘤性蛛网膜下腔出血(aSAH)是死亡或长期残疾的常见原因。尽管神经重症监护取得了进展,但监测继发性脑损伤的发展或预测aSAH后的神经功能结局的能力仍然非常有限。可溶性尿激酶型纤溶酶原激活物受体(suPAR)已显示出作为多种危重病的预后和炎症生物标志物的潜力,因为它与整体免疫系统激活有关。这是首次评估suPAR作为aSAH的预后生物标志物。

方法

在这项基于人群的前瞻性研究中,对47例aSAH患者的血浆suPAR水平进行了长达5天的测量。在患者入住重症监护病房(ICU)后0、12和24小时测量suPAR,此后每天测量,直至其从ICU转出。在aSAH后6个月用改良Rankin量表(mRS)评估患者的神经功能结局。

结果

aSAH后最初24小时内,预后良好(mRS 0-2)或预后不良(mRS 3-6)组的suPAR水平相当。最初24小时内的suPAR水平与原发性脑CT检查结果、急性脑积水或5天随访期间的抗菌药物使用无关。suPAR水平与普遍接受的炎症生物标志物(C反应蛋白、白细胞计数)相关。

结论

血浆suPAR水平与神经功能结局或选定的临床状况均无关。虽然suPAR在几种需要重症监护的疾病中是一种有前景的预后生物标志物,但在aSAH后它并未显示出作为预后生物标志物的任何价值。

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本文引用的文献

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eNeurologicalSci. 2016 Dec 2;6:55-62. doi: 10.1016/j.ensci.2016.11.010. eCollection 2017 Mar.
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Aneurysmal Subarachnoid Hemorrhage and Neuroinflammation: A Comprehensive Review.动脉瘤性蛛网膜下腔出血与神经炎症:全面综述
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Increased plasma UCH-L1 after aneurysmal subarachnoid hemorrhage is associated with unfavorable neurological outcome.
Temporal patterns of inflammation-related proteins measured in the cerebrospinal fluid of patients with aneurysmal subarachnoid hemorrhage using multiplex Proximity Extension Assay technology.
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PLoS One. 2022 Mar 24;17(3):e0263460. doi: 10.1371/journal.pone.0263460. eCollection 2022.
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Admission Lower Serum Phosphate Ion Levels Predict Acute Hydrocephalus of Aneurysmal Subarachnoid Hemorrhage.入院时较低的血清磷酸根离子水平可预测动脉瘤性蛛网膜下腔出血后的急性脑积水。
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Clin Neurol Neurosurg. 2015 Nov;138:177-83. doi: 10.1016/j.clineuro.2015.08.030. Epub 2015 Aug 28.
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Nosocomial infections after aneurysmal subarachnoid hemorrhage: time course and causative pathogens.动脉瘤性蛛网膜下腔出血后的医院感染:时间进程及致病病原体
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Systemic, local, and imaging biomarkers of brain injury: more needed, and better use of those already established?脑损伤的系统、局部和影像学生物标志物:是否需要更多,以及如何更好地利用已经建立的生物标志物?
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