A multicenter, randomized, double-blind, placebo-controlled trial to evaluate the effect of Tongmai Yangxin pill on ventricular remodeling in acute anterior STEMI patients after primary PCI.

IF 6.7 1区 医学 Q1 CHEMISTRY, MEDICINAL Phytomedicine Pub Date : 2024-10-17 DOI:10.1016/j.phymed.2024.156133
Yongxia Wang, Xinlu Wang, Jianru Wang, Chunjie Li, Guoan Zhao, Chaoyang Zheng, Xiaochi Shi, Xiaolong Wang, Ke Wang, Wei Wu, Zhenpeng Zhang, Hengliang Liu, Hao Zhou, Fei Lin, Xiaofen Ruan, Jia Zhao, Shichao Wang, Xingyuan Li, Shanshan Nie, Xiaohui Li, Jinyu Huang, Heng Sun, Linping Pian, Wei Xing, Bin Li, Rui Yu, Zuoying Xing, Yankun Song, Yutian Luo, Duolao Wang, Yanming Xie, Junhua Zhang, Mingjun Zhu
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Abstract

Background: Acute ST-segment elevation myocardial infarction (STEMI) is a severe form of coronary heart disease and a leading cause of mortality and morbidity. This can mainly be ascribed to adverse ventricular remodeling (VR). However, the efficacy of existing treatment strategies for STEMI is not entirely satisfactory. Tongmai Yangxin Pill (TMYX), a patented traditional Chinese medicine (TCM), has been approved for treating various cardiovascular diseases.

Purpose: The purpose was to assess the effect of TMYX on VR in acute STEMI patients undergoing primary percutaneous coronary intervention (PPCI).

Study design: A multicenter, randomized, double-blinded, and placebo-controlled trial conducted across 11 hospitals in China.

Method: A total of 270 patients with acute anterior STEMI, undergoing PPCI within 10 days of symptom onset were enrolled and randomly assigned to receive either a placebo or TMYX, in addition to guideline-directed treatments for STEMI. The primary endpoint was a change in left ventricular end-diastolic volume index (LVEDVI) at 12 weeks.

Result: Among the 270 randomized patients, 218 (TMYX: 109 and placebo: 109) were included in the per-protocol analysis. At 4 and 12 weeks, TXMY significantly improved LVEDVI than the placebo group ([-2.17(-9.24, 8.28) vs. 3.76(-2.38, 11.48), p < 0.05] and [-1.17 (-12.19, 12.88) vs. 4.46 (-2.89, 11.99), p < 0.05]). Changes in left ventricular end-diastolic volume (LVEDV) at 4 weeks were superior in the TMYX group than the placebo group (-4.37 (-17, 13.99) vs. 7.41 (-4.56, 21.79), p < 0.05). Cardiac magnetic resonance imaging (CMRI) showed that left ventricular ejection fraction (LVEF) was significantly greater in the TMYX group than in the placebo group at 4 weeks. There were no statistically significant differences between groups for left ventricular end-systolic volume (LVESV), left ventricular end-systolic volume index (LVESVI), 6 min walking distance (6MWD), and major adverse cardiac and cerebrovascular events (MACCEs) (p > 0.05).

Conclusion: TMYX, as an adjunctive therapy in addition to STEMI guideline-directed treatments, significantly delayed VR in patients with acute anterior STEMI undergoing PPCI within 10 days of symptom onset.

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一项多中心、随机、双盲、安慰剂对照试验,评估通麦养心丸对初级 PCI 后急性前 STEMI 患者心室重构的影响。
背景:急性 ST 段抬高型心肌梗死(STEMI)是冠心病的一种严重形式,也是导致死亡和发病的主要原因。这主要归因于不良的心室重塑(VR)。然而,现有的 STEMI 治疗策略的疗效并不完全令人满意。通脉养心丸(TMYX)是一种专利中药,已被批准用于治疗各种心血管疾病。研究目的:旨在评估通脉养心丸对接受经皮冠状动脉介入治疗(PPCI)的急性 STEMI 患者心室重构的影响:研究设计:一项在中国11家医院开展的多中心、随机、双盲和安慰剂对照试验:共纳入 270 名急性前 STEMI 患者,他们在症状出现后 10 天内接受了 PPCI,除了接受 STEMI 指南指导的治疗外,还被随机分配接受安慰剂或 TMYX。主要终点是12周时左心室舒张末期容积指数(LVEDVI)的变化:结果:在270名随机患者中,218名(TMYX:109名,安慰剂:109名)纳入了按协议分析。在4周和12周时,TXMY对LVEDVI的改善明显优于安慰剂组([-2.17(-9.24, 8.28) vs. 3.76(-2.38, 11.48),p < 0.05]和[-1.17 (-12.19, 12.88) vs. 4.46 (-2.89, 11.99),p < 0.05])。4周时左心室舒张末期容积(LVEDV)的变化,TMYX组优于安慰剂组(-4.37(-17,13.99)vs 7.41(-4.56,21.79),P <0.05)。心脏磁共振成像(CMRI)显示,4周时,TMYX组的左心室射血分数(LVEF)明显高于安慰剂组。在左心室收缩末期容积(LVESV)、左心室收缩末期容积指数(LVESVI)、6 分钟步行距离(6MWD)和主要心脑血管不良事件(MACCEs)方面,组间差异无统计学意义(P > 0.05):结论:TMYX 作为 STEMI 指南指导疗法的辅助疗法,可显著延迟在症状出现后 10 天内接受 PPCI 的急性前 STEMI 患者的 VR。
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来源期刊
Phytomedicine
Phytomedicine 医学-药学
CiteScore
10.30
自引率
5.10%
发文量
670
审稿时长
91 days
期刊介绍: Phytomedicine is a therapy-oriented journal that publishes innovative studies on the efficacy, safety, quality, and mechanisms of action of specified plant extracts, phytopharmaceuticals, and their isolated constituents. This includes clinical, pharmacological, pharmacokinetic, and toxicological studies of herbal medicinal products, preparations, and purified compounds with defined and consistent quality, ensuring reproducible pharmacological activity. Founded in 1994, Phytomedicine aims to focus and stimulate research in this field and establish internationally accepted scientific standards for pharmacological studies, proof of clinical efficacy, and safety of phytomedicines.
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