{"title":"Shenmai injection in treating chemotherapy-related cardiotoxicity of breast cancer: a systematic review and meta-analysis","authors":"Ming Feng , Hong Huang , Chang Yao","doi":"10.1016/j.hermed.2024.100936","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>Shenmai injection (SMI) is an established treatment for cardiac diseases, and we performed to evaluate the efficacy of SMI combined with chemotherapy drugs for the treatment of chemotherapy-induced cardiotoxicity.</div></div><div><h3>Methods</h3><div>The primary outcome was abnormal electrocardiogram (ECG), left ventricular ejection fraction (LVEF) and E/A. The secondary outcomes included myocardial injury biomarkers (creatine kinase [CK], creatine kinase MB [CK-MB], and cardiac troponin I [cTnI]) and lipid peroxide markers (superoxide dismutase [SOD], glutathione [GSH], and malondialdehyde [MAD]).</div></div><div><h3>Results</h3><div>Studies indicated that SMI combined with chemotherapy drugs has advantages over chemotherapy drugs alone in reducing the incidence of abnormal ECG (ST-T: RR = 0.613, 95% CI [0.437, 0.862], <em>P</em> = 0.005; extrasystole: RR = 0.527, 95% CI [0.349, 0.798], <em>P</em> = 0.002). Myocardial injury biomarkers in the experimental group were lower than those in the control group (CK: SMD = –2.614, 95% CI [–3.156, –2.071], <em>P</em> = 0.000; CK-MB: SMD = –6.882, 95% CI [–8.982, –4.782], <em>P</em> = 0.000; cTnI: SMD = –3.610, 95% CI [–4.949, –2.271], <em>P</em> = 0.000). Ultrasonic cardiogram analysis showed that the experimental group had a higher LVEF and E/A than the control group (LVEF: SMD = 1.572, 95% CI [1.176, 1.969], <em>P</em> = 0.000; E/A: SMD = 0.280, 95% CI [0.153, 0.407], <em>P</em> = 0.000). Lipid peroxide meta-analysis showed that the experimental group had higher SOD and GSH levels (SOD: weighted mean difference (WMD) = 39.783, 95% CI (32.524, 47.042), <em>P</em> = 0.000; GSH: WMD = 32.960, 95% CI [26.055, 39.865], <em>P</em> = 0.000), and lower malondialdehyde (MDA) (WMD = –4.962, 95% CI [–6.041, –3.883], <em>P</em> = 0.000).</div></div><div><h3>Conclusion</h3><div>SMI is effective in reducing cardiac injury and the incidence of cardiotoxicity.</div></div>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2210803324000939","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
Abstract
Objective
Shenmai injection (SMI) is an established treatment for cardiac diseases, and we performed to evaluate the efficacy of SMI combined with chemotherapy drugs for the treatment of chemotherapy-induced cardiotoxicity.
Methods
The primary outcome was abnormal electrocardiogram (ECG), left ventricular ejection fraction (LVEF) and E/A. The secondary outcomes included myocardial injury biomarkers (creatine kinase [CK], creatine kinase MB [CK-MB], and cardiac troponin I [cTnI]) and lipid peroxide markers (superoxide dismutase [SOD], glutathione [GSH], and malondialdehyde [MAD]).
Results
Studies indicated that SMI combined with chemotherapy drugs has advantages over chemotherapy drugs alone in reducing the incidence of abnormal ECG (ST-T: RR = 0.613, 95% CI [0.437, 0.862], P = 0.005; extrasystole: RR = 0.527, 95% CI [0.349, 0.798], P = 0.002). Myocardial injury biomarkers in the experimental group were lower than those in the control group (CK: SMD = –2.614, 95% CI [–3.156, –2.071], P = 0.000; CK-MB: SMD = –6.882, 95% CI [–8.982, –4.782], P = 0.000; cTnI: SMD = –3.610, 95% CI [–4.949, –2.271], P = 0.000). Ultrasonic cardiogram analysis showed that the experimental group had a higher LVEF and E/A than the control group (LVEF: SMD = 1.572, 95% CI [1.176, 1.969], P = 0.000; E/A: SMD = 0.280, 95% CI [0.153, 0.407], P = 0.000). Lipid peroxide meta-analysis showed that the experimental group had higher SOD and GSH levels (SOD: weighted mean difference (WMD) = 39.783, 95% CI (32.524, 47.042), P = 0.000; GSH: WMD = 32.960, 95% CI [26.055, 39.865], P = 0.000), and lower malondialdehyde (MDA) (WMD = –4.962, 95% CI [–6.041, –3.883], P = 0.000).
Conclusion
SMI is effective in reducing cardiac injury and the incidence of cardiotoxicity.
方法 主要结果是心电图(ECG)异常、左室射血分数(LVEF)和E/A。次要结果包括心肌损伤生物标志物(肌酸激酶[CK]、肌酸激酶MB[CK-MB]和心肌肌钙蛋白I[cTnI])和过氧化脂质标志物(超氧化物歧化酶[SOD]、谷胱甘肽[GSH]和丙二醛[MAD])。结果研究表明,SMI联合化疗药物在降低异常心电图(ST-T:RR=0.613,95% CI [0.437,0.862],P=0.005;期外收缩:RR=0.527,95% CI [0.349,0.798],P=0.002)。实验组心肌损伤生物标志物低于对照组(CK:SMD = -2.614,95% CI [-3.156,-2.071],P = 0.000;CK-MB:SMD = -6.882,95% CI [-8.982,-4.782],P = 0.000;cTnI:SMD = -3.610,95% CI [-4.949,-2.271],P = 0.000)。超声心动图分析显示,实验组的 LVEF 和 E/A 均高于对照组(LVEF:SMD=1.572,95% CI [1.176,1.969],P=0.000;E/A:SMD=0.280,95% CI [0.153,0.407],P=0.000)。过氧化脂质荟萃分析表明,实验组的 SOD 和 GSH 水平更高(SOD:加权平均差(WMD)= 39.783,95% CI [32.524,47.042],P = 0.000;GSH:WMD = 32.960,95% CI [26.结论SMI能有效降低心脏损伤和心脏毒性的发生率。