Zheng Qun, Zhuang Zhuang, Wang Zi-Hao, Deng Li-Hui, Jin Wang-Jun, Huang Zi-Jun, Zheng Guo-Qing, Wang Yan
Department of Rheumatism and Immunity, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Department of Cardiology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Oxid Med Cell Longev. 2020 Nov 2;2020:1560353. doi: 10.1155/2020/1560353. eCollection 2020.
Astragalus membranaceus (AM) is a traditional Chinese medicine, which possesses a variety of biological activities in the cardiovascular systems. We conducted a clinical and preclinical systematic review of 28 randomized clinical control studies with 2522 participants and 16 animal studies with 634 animals to evaluate the efficacy, safety, and possible mechanisms of AM for viral myocarditis (VM). The search strategies were performed in 7 databases from inception to January 2020. Application of the Cochrane Collaboration's tool 7-item checklist, SYRCLE's tool 10-item checklist, and Rev-Man 5.3 software to analyze the risk of bias of studies and data. The results show the score of clinical study quality ranged from 3 to 7 points with an average of 3.32, and the score of animal study quality ranged from 2 to 5 points with an average of 3. In clinical study, AM significantly reduced serum myocardial enzymes and cardiac troponin I levels and improved the clinical treatment efficiency in VM patients compared with the control group ( < 0.05). There was no significant difference in the incidence of adverse reactions ( > 0.05). Significant increase of the survival rate and decrease of the cardiac cardiology score, cardiac enzymes, and cardiac troponin I were compared with the placebo group in animal studies ( < 0.05). The possible mechanisms of AM are largely through antivirus and antivirus receptors, anti-inflammatory, antioxidation, antiapoptotic, antifibrosis, and reducing cardiac calcium load. In conclusion, the findings suggested that AM is a cardioprotection candidate drug for VM.
黄芪是一种传统中药,在心血管系统中具有多种生物活性。我们对28项随机临床对照研究(涉及2522名参与者)和16项动物研究(涉及634只动物)进行了临床和临床前系统评价,以评估黄芪治疗病毒性心肌炎(VM)的疗效、安全性及可能机制。检索策略在7个数据库中从建库至2020年1月实施。应用Cochrane协作网工具的7项清单、SYRCLE工具的10项清单以及Rev-Man 5.3软件分析研究和数据的偏倚风险。结果显示,临床研究质量得分在3至7分之间,平均为3.32分;动物研究质量得分在2至5分之间,平均为3分。在临床研究中,与对照组相比,黄芪显著降低了VM患者的血清心肌酶和心肌肌钙蛋白I水平,并提高了临床治疗有效率(<0.05)。不良反应发生率无显著差异(>0.05)。在动物研究中,与安慰剂组相比,黄芪显著提高了生存率,降低了心脏评分、心肌酶和心肌肌钙蛋白I水平(<0.05)。黄芪的可能机制主要是通过抗病毒及其受体、抗炎、抗氧化、抗凋亡、抗纤维化以及减轻心脏钙负荷。总之,研究结果表明黄芪是VM的一种心脏保护候选药物。