脑苷肌肽联合重组人组织型纤溶酶原激活物静脉溶栓对急性缺血性脑卒中患者血清超敏C反应蛋白、胰岛素样生长因子-1水平的影响

段淑娟, 王雁飞

段淑娟, 王雁飞. 脑苷肌肽联合重组人组织型纤溶酶原激活物静脉溶栓对急性缺血性脑卒中患者血清超敏C反应蛋白、胰岛素样生长因子-1水平的影响[J]. 实用临床医药杂志, 2019, 23(20): 11-14. DOI: 10.7619/jcmp.201920003
引用本文: 段淑娟, 王雁飞. 脑苷肌肽联合重组人组织型纤溶酶原激活物静脉溶栓对急性缺血性脑卒中患者血清超敏C反应蛋白、胰岛素样生长因子-1水平的影响[J]. 实用临床医药杂志, 2019, 23(20): 11-14. DOI: 10.7619/jcmp.201920003
DUAN Shujuan, WANG Yanfei. Influence of cerebroside carnosine combined with intravenous thrombolysis with recombinant human tissue plasminogen activator on serum high-sensitivity C reactive protein and insulin-like growth factor-1 levels in patients with acute ischemic stroke[J]. Journal of Clinical Medicine in Practice, 2019, 23(20): 11-14. DOI: 10.7619/jcmp.201920003
Citation: DUAN Shujuan, WANG Yanfei. Influence of cerebroside carnosine combined with intravenous thrombolysis with recombinant human tissue plasminogen activator on serum high-sensitivity C reactive protein and insulin-like growth factor-1 levels in patients with acute ischemic stroke[J]. Journal of Clinical Medicine in Practice, 2019, 23(20): 11-14. DOI: 10.7619/jcmp.201920003

脑苷肌肽联合重组人组织型纤溶酶原激活物静脉溶栓对急性缺血性脑卒中患者血清超敏C反应蛋白、胰岛素样生长因子-1水平的影响

详细信息
    通讯作者:

    王雁飞

  • 中图分类号: R743.3

Influence of cerebroside carnosine combined with intravenous thrombolysis with recombinant human tissue plasminogen activator on serum high-sensitivity C reactive protein and insulin-like growth factor-1 levels in patients with acute ischemic stroke

  • 摘要:
      目的  探讨脑苷肌肽联合重组人组织型纤溶酶原激活物(rt-PA)静脉溶栓对急性缺血性脑卒中患者血清超敏C反应蛋白(hs-CRP)、胰岛素样生长因子-1(IGF-1)水平的影响。
      方法  选取120例急性缺血性脑卒中患者, 随机分为2组各60例。对照组采取rt-PA静脉溶栓治疗,研究组在对照组基础上加用脑苷肌肽注射液。比较2组治疗前及疗程结束后的日常生活能力(ADL)及美国国立卫生研究院卒中量表(NIHSS)评分、临床疗效、血清hs-CRP、IGF-1水平以及不良反应发生率。
      结果  研究组总有效率91.67%, 显著高于对照组71.67%(P < 0.05)。2组疗程结束后NIHSS较治疗前显著降低, ADL较治疗前显著增高,且研究组显著优于对照组(P < 0.05)。疗程结束后, 2组IGF-1水平显著高于治疗前, hs-CRP显著低于治疗前,且研究组显著优于对照组(P < 0.05)。研究组不良反应发生率15.00%, 与对照组11.67%比较无显著差异(P>0.05)。
      结论  应用rt-PA静脉溶栓联合脑苷肌肽注射液治疗急性缺血性脑卒中安全有效,可调节血清hs-CRP、IGF-1水平,改善神经功能及提高日常生活能力,且不会增加不良反应发生率。
    Abstract:
      Objective  To investigate the influence of cerebroside carnosine combined with intravenous thrombolysis with recombinant human tissue plasminogen activator (rt-PA) on serum high-sensitivity C reactive protein (hs-CRP) and insulin-like growth factor-1 (IGF-1) levels in patients with acute ischemic stroke.
      Methods  A total of 120 patients with acute ischemic stroke were selected and randomly divided into two groups, with 60 cases in each group. The control group was treated with rt-PA intravenous thrombolysis, while the study group was treated with cerebroside carnosine injection on the basis of the control group. The scores of Activities of Daily Living (ADL) and National Institutes of Health Stroke Scale (NIHSS), clinical efficacy, serum hs-CRP and IGF-1 levels, and the incidence rate of adverse reactions were compared between the two groups before and after treatment.
      Results  The total effective rate was 91.67% in the study group, which was significantly higher than 71.67% in the control group (P < 0.05). After treatment, the NIHSS score was significantly lower and ADL was significantly higher in both groups, and the scores in study group were significantly better than the control group (P < 0.05). After treatment, the levels of IGF-1 and hs-CRP in both groups were significantly higher than those before treatment, and the level of hs-CRP in the study group was significantly higher than that in the control group (P < 0.05). The incidence rate of adverse reactions in the study group was 15.00%, which showed no significant difference when compared to 11.67% in the control group (P>0.05).
      Conclusion  Application of rt-PA intravenous thrombolysis combined with cerebroside carnosine injection is safe and effective in the treatment of acute ischemic stroke, which can regulate the levels of serum hs-CRP and IGF-1, improve nerve function and daily living ability, and does not increase the incidence rate of adverse reactions.
  • 表  1   2组临床疗效比较[n(%)]

    组别 n 显效 有效 无效 总有效
    研究组 60 29(48.33) 26(43.33) 5(8.33) 55(91.67)*
    对照组 60 21(35.00) 22(36.67) 17(28.33) 43(71.67)
        与对照组比较, *P < 0.05。
    下载: 导出CSV

    表  2   2组NIHSS及ADL评分比较(x±s)  

    组别 n NIHSS ADL
    治疗前 疗程结束后 治疗前 疗程结束后
    研究组 60 20.07±2.01 6.47±0.95*# 40.67±10.10 70.39±7.30*#
    对照组 60 20.23±1.95 8.66±1.11* 41.02±10.29 61.34±6.43*
    NIHSS: 美国国立卫生研究院卒中量表; ADL: 日常生活活动能力量表。与治疗前比较, *P < 0.05; 与对照组比较, #P < 0.05。
    下载: 导出CSV

    表  3   2组血清hs-CRP及IGF-1水平比较(x±s)

    组别 n hs-CRP/(mg/L) IGF-1/(ng/mL)
    治疗前 疗程结束后 治疗前 疗程结束后
    研究组 60 12.34±3.41 3.19±0.87*# 32.86±4.14 56.15±5.69*#
    对照组 60 12.53±3.53 4.64±1.01* 33.20±4.24 45.26±5.11*
    hs-CRP: 超敏C反应蛋白; IGF-1: 胰岛素样生长因子-1。与治疗前比较, *P < 0.05; 与对照组比较, #P < 0.05。
    下载: 导出CSV

    表  4   2组不良反应发生情况比较[n(%)]

    组别 n 呕吐 转氨酶增高 皮疹 恶心 总计
    研究组 60 3(5.00) 3(5.00) 1(1.67) 2(3.33) 9(15.00)
    对照组 60 1(1.67) 1(1.67) 2(3.33) 3(5.00) 7(11.67)
    下载: 导出CSV
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出版历程
  • 收稿日期:  2019-08-11
  • 录用日期:  2019-09-24
  • 网络出版日期:  2021-02-28
  • 发布日期:  2019-10-27

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