Wu Yang, Li Tianli, Li Pochen, Peng HsuanChieh, Gao Ang, Wang Jisheng, Zhu Haiyan, Wang Xian
Department of Cardiology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
National Integrated Traditional and Western Medicine Center for Cardiovascular Disease, China-Japan Friendship Hospital, Beijing, China.
Front Pharmacol. 2024 Feb 6;14:1338975. doi: 10.3389/fphar.2023.1338975. eCollection 2023.
This study aims to evaluate the clinical and preclinical efficacy of SMI in treating CHF, and to summarize the relevant mechanisms of action in order to provide evidence for its role in CHF treatment. A systematic computerized search of eight databases and three registry systems was performed, with the time frame spanning from the inception of the databases to 30 June 2023. Strict procedures were used for data extraction, quality assessment, and data analysis. The methodological quality of the included studies was assessed using RoB-2 and SYRCLE tools. Statistical analysis was performed using Rev Man 5.4 software, using either fixed-effects or random-effects models. A total of 25 clinical trials (including test group 1,367 patients, control group 1,338 patients) and 11 animal studies (including 201 animals) were included in this review. The meta-analysis of clinical studies showed that SMI can improve cardiac function indicators (LVEF, LVFS, LVEDV, LVESV, LVEDD, LVESD) ( < 0.00001), reduce BNP/NT-proBNP levels ( < 0.01), and improve inflammatory markers (hs-CRP, TNF-α, IL-6) ( < 0.00001) and endothelin (ET) levels ( < 0.0001). In animal studies, SMI demonstrated improved cardiac function (LVEF, LVFS) ( < 0.05), and improved heart failure markers (NT-proBNP, < 0.05) when compared to control groups. This study represents the first meta-analysis which includes both preclinical and clinical studies on SMI. Clinical and animal studies have shown that SMI can improve cardiac function in CHF patients through its anti-apoptotic effects, antioxidant activities, anti-inflammatory effects, and improvement of myocardial metabolism. This study has certain limitations in terms of literature quality, quantity, and follow-up time. Therefore, the conclusions drawn from this study may require further validation through larger-scale, high-quality RCT trials.
本研究旨在评估参麦注射液(SMI)治疗慢性心力衰竭(CHF)的临床和临床前疗效,并总结其相关作用机制,为其在CHF治疗中的作用提供依据。对八个数据库和三个注册系统进行了系统的计算机检索,时间范围从数据库建立至2023年6月30日。采用严格的程序进行数据提取、质量评估和数据分析。使用RoB-2和SYRCLE工具评估纳入研究的方法学质量。使用Rev Man 5.4软件进行统计分析,采用固定效应或随机效应模型。本综述共纳入25项临床试验(试验组1367例患者,对照组1338例患者)和11项动物研究(包括201只动物)。临床研究的荟萃分析表明,SMI可改善心功能指标(左心室射血分数、左心室短轴缩短率、左心室舒张末期容积、左心室收缩末期容积、左心室舒张末期内径、左心室收缩末期内径)(P<0.00001),降低脑钠肽/氨基末端脑钠肽前体水平(P<0.01),并改善炎症标志物(高敏C反应蛋白、肿瘤坏死因子-α、白细胞介素-6)(P<0.00001)和内皮素(ET)水平(P<0.0001)。在动物研究中,与对照组相比,SMI显示出改善的心功能(左心室射血分数、左心室短轴缩短率)(P<0.05),以及改善的心力衰竭标志物(氨基末端脑钠肽前体,P<0.05)。本研究是第一项纳入SMI临床前和临床研究的荟萃分析。临床和动物研究表明,SMI可通过其抗凋亡作用、抗氧化活性、抗炎作用和改善心肌代谢来改善CHF患者的心功能。本研究在文献质量、数量和随访时间方面存在一定局限性。因此,本研究得出的结论可能需要通过更大规模、高质量的随机对照试验进一步验证。