Sabir Rashid Avan, Huang-Link Yumin, Johnsson Marcus, Wetterhäll Simon, Gauffin Helena
Department of Biomedical and Clinical Sciences (BKV), Faculty of Medicine and Health Sciences, Linköping University, Linköping, Sweden.
Department of Neurology, Linköping University Hospital, Region Östergötland, Linköping, Sweden.
Neuropsychiatr Dis Treat. 2022 Sep 6;18:1993-2002. doi: 10.2147/NDT.S365758. eCollection 2022.
Early neurological deterioration (END) in acute ischemic stroke (AIS) can be associated with poor outcome. The aim of this study was to investigate the association between infarction subtypes, biomarkers and END, and to identify patients with risk of unfavorable functional outcome.
This prospective study enrolled 101 patients with AIS. Neurological status was evaluated according to NIHSS at acute onset, on days 2, 3, and 90. END was defined as ≥2-point increase of NIHSS within 72 hours. Functional outcome was assessed using NIHSS and the modified Rankin Scale (mRS) at day 90.
END was observed in 20, 8%. Patients with large artery disease had higher risk of developing END compared with patients with cardioembolism or small vessel disease (p <0.01). Significant higher blood glucose level and leukocytes were observed in the END group. Patients with END had higher scores of mRS at day 90 (p <0.01). Levels of NSE, IL-6, hsCRP and NT-proBNP were higher in the patients with unfavorable compared with favorable functional outcome.
Large artery disease, high blood glucose and leukocytes levels are associated with END. Elevated levels of blood markers NSE, IL-6, HsCRP and NT-proBNP indicate poor functional outcome at 90 days after AIS. These patients must be identified and be offered treatment immediately in order to improve the functional outcome after AIS.
急性缺血性卒中(AIS)早期神经功能恶化(END)可能与不良预后相关。本研究旨在探讨梗死亚型、生物标志物与END之间的关联,并识别功能预后不良风险的患者。
这项前瞻性研究纳入了101例AIS患者。在急性发病时、第2天、第3天和第90天根据美国国立卫生研究院卒中量表(NIHSS)评估神经功能状态。END定义为72小时内NIHSS评分增加≥2分。在第90天使用NIHSS和改良Rankin量表(mRS)评估功能预后。
观察到20例(8%)出现END。与心源性栓塞或小血管疾病患者相比,大动脉疾病患者发生END的风险更高(p<0.01)。END组的血糖水平和白细胞显著更高。END患者在第90天的mRS评分更高(p<0.01)。功能预后不良的患者中,神经元特异性烯醇化酶(NSE)、白细胞介素-6(IL-6)、高敏C反应蛋白(hsCRP)和N末端脑钠肽前体(NT-proBNP)水平更高。
大动脉疾病、高血糖和白细胞水平与END相关。血液标志物NSE、IL-6、HsCRP和NT-proBNP水平升高表明AIS后90天功能预后不良。必须识别出这些患者并立即给予治疗,以改善AIS后的功能预后。