Kiiski Heikki, Jalkanen Ville, Ala-Peijari Marika, Hämäläinen Mari, Moilanen Eeva, Peltola Jukka, Tenhunen Jyrki
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.
Front Neurol. 2017 Apr 18;8:144. doi: 10.3389/fneur.2017.00144. eCollection 2017.
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.
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.
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).
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.
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。
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。
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。
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。