河北医科大学学报 ›› 2024, Vol. 45 ›› Issue (3): 348-354.doi: 10.3969/j.issn.1007-3205.2024.03.016

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脑梗死患者静脉溶栓疗程中VILIP-1、Annexin A2、sEPCR动态变化及与病情转归相关性

  

  1. 云南省第三人民医院神经内科,云南 昆明 650200

  • 出版日期:2024-03-25 发布日期:2024-04-07
  • 作者简介:李词(1982-),男,四川万源人,云南省第三人民医院主治医师,医学学士,从事神经内科疾病诊治研究。
  • 基金资助:
    云南省科技厅科技计划项目(202001BA070023-0077)

Dynamic changes of VILIP-1, Annexin A2 and sEPCR during intravenous thrombolytic therapy in patients with cerebral infarction and their correlation with outcome of disease

  1. Department of Neurology, the Third People′s Hospital of Yunnan Province, Kunming 650200, China

  • Online:2024-03-25 Published:2024-04-07

摘要: 目的 探讨脑梗死患者静脉溶栓疗程中视椎蛋白样蛋白1(visinin like protein-1,VILIP-1)、膜联蛋白A2(Annexin A2)、可溶性血管内皮蛋白C受体(solubleendothelium protein c receptor,sEPCR)动态变化及与病情转归相关性,为临床预测、改善患者预后提供参考。
方法 选取急性脑梗死患者105例进行前瞻性研究,均接受静脉溶栓治疗。以门诊方式随访28 d,根据患者病情转归情况分为良好组、不良组,检测2组溶栓前、溶栓后1 d、3 d的VILIP-1、Annexin A2、sEPCR水平,分析其与mRS评分的相关性,随机森林算法筛选特征变量,并分析病情转归的影响因素,分析不同时间点VILIP-1、Annexin A2、sEPCR及联合预测病情转归价值。
结果 不良组美国国立卫生研究院卒中量表(National Institutes of Health Stroke Scale,NIHSS)评分、D-二聚体、纤维蛋白原、三酰甘油高于良好组(P<0.05)。2组VILIP-1、sEPCR水平随着溶栓时间的延长而减低,Annexin A2随着溶栓时间的延长而升高(P<0.05);不良组VILIP-1、sEPCR和Annexin A2波动高于良好组(P<0.05)。溶栓后1 d、溶栓后3 d的VILIP-1、sEPCR与mRS评分呈正相关,Annexin A2与mRS评分呈负相关(P<0.05)。选取决策树数量ntree为390颗,得到最优结果,重要性排序前4的变量分别是sEPCR、Annexin A2、NIHSS评分、VILIP-1,均与mRS评分相关(P<0.05);溶栓后3 d三者联合的AUC最大,其预测敏感度为78.79%,特异度为95.83%。
结论 血清VILIP-1、Annexin A2、sEPCR异常表达与脑梗死患者脑损伤程度、溶栓预后有关,溶栓后3 d联合检测的预后价值较高,可作为脑梗死患者预后预测的重要标志物。


关键词:  , 脑梗死, 血栓溶解疗法, 视椎蛋白样蛋白1

Abstract: Objective To investigate the dynamic changes of Visinin-like protein-1 (VILIP-1), Annexin A2 and soluble endothelium protein c receptor (sEPCR) during the course of intravenous thrombolytic therapy in patients with cerebral infarction and their correlation with outcome of disease, so as to provide reference for clinical prediction and improvement of patient prognosis. 
Methods One hundred and five patients with acute cerebral infarction (ACI) were selected for a prospective study, and all received intravenous thrombolytic therapy. The patients were followed up during outpatient visit for 28 d. The patients were divided into good and poor groups according to their outcome of disease, and the levels of VILIP-1, Annexin A2, and sEPCR were detected before thrombolysis, and at 1 d and 3 d after thrombolysis in both groups, to analyze their correlation with mRS score. The characteristic variables were screened by random forest algorithm, and the influencing factors of outcome of disease were analyzed. In addition, the value of VILIP-1, Annexin A2, and sEPCR alone and in combination in predicting the outcome of disease at different time points were analyzed. 
Results The National Institutes of Health Stroke Scale (NIHSS) score, D-dimer (DD), fibrinogen, and triglycerides in the poor group were higher than those in the good group (P<0.05). The levels of VILIP-1 and sEPCR in the two groups decreased with the prolongation of thrombolysis time, while Annexin A2 increased with the prolongation of thrombolysis time (P<0.05). The VILIP-1, sEPCR, and Annexin A2 fluctuations in the poor group were higher than those in the good group (P<0.05). VILIP-1 and sEPCR were positively correlated with mRS scores at 1 day and 3 days after thrombolysis, while Annexin A2 was negatively correlated with mRS scores (P<0.05). Selecting 390 decision trees, the optimal result was obtained. The top 4 variables in importance ranking were sEPCR, Annexin A2, NIHSS score, and VILIP-1, all of which were correlated with mRS score (P<0.05). At 3 days after thrombolysis, the combination of the three had the highest AUC, with a predictive sensitivity of 78.79% and a specificity of 95.83%. 
Conclusion Abnormal expression of serum VILIP-1, Annexin A2 and sEPCR is related to the degree of brain injury and prognosis of thrombolysis in patients with cerebral infarction, and the prognostic value of the combined detection at 3 d after thrombolysis is higher, which can be used as an important marker for prognosis prediction in patients with cerebral infarction. 


Key words: brain infarction, thrombolytic therapy, Visinin-like protein-1