依洛尤单抗和阿利西尤单抗治疗急性冠状动脉综合征的网状meta分析

    Treatment of Evolocumab and Alirocumab on Acute Coronary Syndrome: A Network Meta-analysis

    • 摘要:
      目的  评价依洛尤单抗和阿利西尤单抗治疗急性冠状动脉综合征(acute coronary syndrome,ACS)的有效性、安全性。
      方法 检索国内外公开发表的依洛尤单抗和阿利西尤单抗治疗ACS的随机对照试验(randomized controlled trials,RCT),检索时限从建库至2023年6月,应用Stata 15软件进行网状meta分析比较两药之间的有效性和安全性。
      结果 共纳入22个RCT,包括22339例患者。试验组药物为他汀类药物联合依洛尤单抗或阿利西尤单抗任意1种,对照组为单用他汀类药物或联合安慰剂。有效性方面,在他汀类药物的基础上,依洛尤单抗和阿利西尤单抗在降低LDL-C、TG、TC、hs-CRP水平以及改善HDL-C代谢方面,两者均无显著差异。安全性方面,两药的心血管不良事件发生率均无显著性差异。
      结论 在ACS患者中,他汀联合依洛尤单抗或阿利西尤单抗治疗可明显改善脂质代谢,减少心血管不良事件的发生。两药之间的有效性和安全性比较差异无统计学意义。但本结论仍需大量多中心、大样本的RCT予以验证。

       

      Abstract:
      OBJECTIVE  To evaluate the efficacy and safety of evolocumab and alirocumab on the treatment of acute coronary syndrome(ACS).
      METHODS  Retrieve randomized controlled trials(RCTs) of evolocumab and alirocumab for the treatment of ACS that have been publicly published both domestically and internationally, with a search period from database establishment to June 2023. Used Stata 15 software to conduct a network meta-analysis to compare the efficacy and safety of evolocumab and alirocumab.
      RESULTS  A total of 22 RCTs, involving 22339 patients were included. The drugs in the experimental group included statins combined with either evolocumab or alirocumab, and the control group was statins or statins combined with placebo. In terms of effectiveness, on the basis of statins, there was no significant difference in the reduction of LDL-C, TG, TC, hs-CRP levels and improvement of HDL-C metabolism between evolocumab and alirocumab. In terms of safety, there was no significant difference in the incidence of cardiovascular adverse events between the two drugs.
      CONCLUSION  In the ACS population, statin combined with evolocumab or alirocumab significantly improve lipid metabolism and reduce the incidence of adverse cardiovascular events. There is no significant difference in the incidence of efficacy and safety between the evolocumab or alirocumab. However, this conclusion still needs to be validated through a large number of multicenter and large sample RCTs.

       

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