首页> 外文期刊>Journal of Translational Medicine >Comparison of acute versus convalescent stage high-sensitivity C-Reactive protein level in predicting clinical outcome after acute ischemic stroke and impact of erythropoietin
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Comparison of acute versus convalescent stage high-sensitivity C-Reactive protein level in predicting clinical outcome after acute ischemic stroke and impact of erythropoietin

机译:急性期与恢复期高敏C反应蛋白水平在预测急性缺血性中风后的临床结局及促红细胞生成素的影响方面的比较

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Background and Aim Currently, no data on the optimal time point after acute ischemic stroke (IS) at which high-sensitivity C-reactive protein (hs-CRP) level is most predictive of unfavorable outcome. We tested the hypothesis that hs-CRP levels during both acute (48 h after IS) and convalescent (21 days after IS) phases are equally important in predicting 90-day clinical outcome after acute IS. We further evaluated the impact of erythropoietin (EPO), an anti-inflammatory agent, on level of hs-CRP after acute IS. Methods Totally 160 patients were prospectively randomized to receive either EPO therapy (group 1, n = 80) (5,000 IU each time, subcutaneously) at 48 h and 72 h after acute IS, or placebo (group 2, n = 80). Serum level of hs-CRP was determined using ELISA at 48 h and on day 21 after IS and once in 60 healthy volunteers. Results Serum level of hs-CRP was substantially higher in all patients with IS than in healthy controls at 48 h and day 21 after IS (all p 0.5). Multivariate analysis showed that hs-CRP levels (at 48 h and day 21) were independently predictive of 90-day major adverse neurological event (MANE) (defined as recurrent stroke, NIHSS≥8, or death) (all p Conclusion EPO therapy which was independently predictive of freedom from 90-day MANE did not alter the crucial role of hs-CRP levels measured at 48 h and 21-day in predicting unfavorable clinical outcome after IS.
机译:背景和目的目前,尚无急性缺血性卒中(IS)后最佳时间点的数据,在该时间点高敏C反应蛋白(hs-CRP)水平最能预测不良结果。我们测试了以下假设:急性期(IS后48小时)和恢复期(IS后21天)的hs-CRP水平对于预测急性IS后90天的临床结局同样重要。我们进一步评估了抗炎药促红细胞生成素(EPO)对急性IS后hs-CRP水平的影响。方法前瞻性将总共160例患者随机分为两组,分别在急性IS后48 h和72 h接受EPO治疗(第1组,n = 80)(每次5,000 IU,皮下注射)或安慰剂(第2组,n = 80)。在60例健康志愿者中,在IS后48小时和第21天使用ELISA测定hs-CRP的血清水平。结果在IS后48小时和21天,所有IS患者的hs-CRP水平均显着高于健康对照者(均P = 0.5)。多变量分析显示,hs-CRP水平(在第48小时和第21天)独立预测90天的主要不良神经事件(MANE)(定义为复发性中风,NIHSS≥8或死亡)(所有p结论可以独立预测90天MANE的自由度不会改变在48h和21天测量的hs-CRP水平在预测IS术后不良临床预后中的关键作用。

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