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急性心肌梗死后早期应用沙库巴曲缬沙坦钠对心室重构及 TGF-β1/Smad3 信号通路的影响。

Early Application of Sacubitril Valsartan Sodium After Acute Myocardial Infarction and its Influence on Ventricular Remodeling and TGF-β1/Smad3 Signaling Pathway.

出版信息

Altern Ther Health Med. 2024 Aug;30(8):98-103.

Abstract

OBJECTIVE

The objective of this study was to investigate the early application of sacubitril valsartan sodium (LCZ696) following acute myocardial infarction (AMI) and its impact on ventricular remodeling and the TGF-β1/Smad3 signaling pathway in patients.

METHODS

The clinical data of 73 patients with AMI admitted to the hospital from June 2021 to September 2022 were retrospectively analyzed, and the patients were grouped according to the treatment methods, including 36 cases in the control group (conventional drug treatment) and 37 cases in the observation group (conventional drug + LCZ696 treatment). The clinical efficacy, cardiac function parameters [left ventricular ejection fraction (LVEF), left ventricular end-diastolic diameter (LVEDD), stroke volume (SV)], cardiac function biochemical indicators [N-terminal pro-B-type natriuretic peptide (NT-proBNP), galectin 3 (Gal-3), amino-terminal peptide of type III procollagen (PIIINP)], ventricular remodeling indicators [left ventricular posterior wall end-diastolic thickness (PWD), posterior wall end-systolic thickness (PWS), ventricular septal end-systolic thickness (IVSS)], ventricular hydrodynamic parameters [left ventricular flow rate in peak ejection (FRPE), flow reversal rate (FRR), flow reversal interval (FRI)], TGF-β 1/Smad3 signaling pathway-related indicators (TGF-β1, Smad3), quality of life score (SF-36 Quality of Life Scale) and occurrence of adverse reactions were compared between the two groups.

RESULTS

The main findings of the study are as follows: The observation group was significantly better than the control group in many aspects such as overall clinical effectiveness, cardiac function parameters, biochemical indicators, ventricular structure and function, TGF-β1/Smad3 signaling pathway, and quality of life. Specifically, the observation group showed more significant positive effects in terms of improvement of cardiac function, adjustment of biochemical status, and adjustment of ventricular structure and fluid dynamics parameters. These results provide strong support for the application of new therapeutic approaches in the management of cardiovascular disease. After treatment, the total clinical effective rate in the observation group (89.19%) was significantly higher than that in the control group (69.44%) (P < .05). LVEF and SV in the two groups were significantly increased (P < .05), while LVEDD was significantly decreased (P < .05), and there were statistically significant differences in parameters between the two groups (P < .05). The levels of NT-proBNP, Gal-3 and PIIINP in both groups were significantly reduced (P < .05), and the levels in the observation group were significantly lower than those in the control group (P < .05). The PWD, PWS and IVSS in both groups significantly declined (P < .05), and the indicators in the observation group were significantly lower than those in the control group (P < .05). The FRPE and FRR in the two groups were significantly enhanced (P < .05), while the FRI was significantly reduced (P < .05), and the differences in the above parameters between the two groups were statistically significant (P < .05). The levels of TGF-β1 and Smad3 in the two groups were significantly declined (P < .05), and the levels in the observation group were significantly lower than those in the control group (P < .05). During the period from before treatment to 6 months of treatment, the quality of life score in the two groups showed a significant downward trend (P < .05), and the score in the observation group after 3 months to 6 months of treatment was significantly lower than that in the control group (P < .05). During treatment, there was no statistical significance in the total incidence rate of adverse reactions between the two groups (P > .05).

CONCLUSION

Early application of LCZ696 after AMI has a significant efficacy, and it can effectively improve the ventricular remodeling, regulate the expression levels of TGF-β1 and Smad3, inhibit the TGF-β1/Smad3 signaling pathway, promote the improvements of cardiac function and quality of life, and it has good safety and is worthy of clinical promotion and application. The study's key findings have important clinical implications for understanding and managing acute myocardial infarction (AMI). The observation group showed significant improvements in overall clinical efficacy, cardiac function, biochemical status, ventricular structure and function, etc., providing strong evidence for comprehensive treatment of AMI patients. This treatment method is expected to become an important part of the care and treatment strategy for AMI patients, help reduce cardiovascular risk, improve quality of life, and provide new research directions for future AMI treatment.

摘要

目的

本研究旨在探讨急性心肌梗死(AMI)后早期应用沙库比曲缬沙坦钠(LCZ696)及其对患者心室重构和 TGF-β1/Smad3 信号通路的影响。

方法

回顾性分析 2021 年 6 月至 2022 年 9 月我院收治的 73 例 AMI 患者的临床资料,根据治疗方法分组,对照组(常规药物治疗)36 例,观察组(常规药物+LCZ696 治疗)37 例。比较两组临床疗效、心功能参数[左心室射血分数(LVEF)、左心室舒张末期直径(LVEDD)、每搏量(SV)]、心功能生化指标[N 端脑利钠肽前体(NT-proBNP)、半乳糖凝集素 3(Gal-3)、III 型前胶原氨基端肽(PIIINP)]、心室重构指标[左心室后壁舒张末期厚度(PWD)、后壁收缩末期厚度(PWS)、室间隔收缩末期厚度(IVSS)]、心室动力学参数[左心室射血峰值流量(FRPE)、流量反转率(FRR)、流量反转间隔(FRI)]、TGF-β1/Smad3 信号通路相关指标(TGF-β1、Smad3)、生活质量评分(SF-36 生活质量量表)及不良反应发生情况。

结果

主要研究结果如下:观察组在整体临床疗效、心功能参数、生化指标、心室结构和功能、TGF-β1/Smad3 信号通路以及生活质量等方面均明显优于对照组。具体而言,观察组在心功能改善、生化状态调节以及心室结构和流体动力学参数调节方面表现出更显著的积极效果。治疗后观察组总有效率(89.19%)明显高于对照组(69.44%)(P<0.05)。两组 LVEF 和 SV 均明显升高(P<0.05),LVEDD 明显降低(P<0.05),两组间参数比较差异均有统计学意义(P<0.05)。两组 NT-proBNP、Gal-3 和 PIIINP 水平均明显降低(P<0.05),观察组水平明显低于对照组(P<0.05)。两组 PWD、PWS 和 IVSS 均明显下降(P<0.05),观察组指标明显低于对照组(P<0.05)。两组 FRPE 和 FRR 均明显增强(P<0.05),FRI 明显降低(P<0.05),两组上述参数比较差异均有统计学意义(P<0.05)。两组 TGF-β1 和 Smad3 水平均明显下降(P<0.05),观察组水平明显低于对照组(P<0.05)。两组治疗期间生活质量评分均呈下降趋势(P<0.05),观察组治疗后 3 个月至 6 个月评分明显低于对照组(P<0.05)。两组不良反应总发生率比较差异无统计学意义(P>0.05)。

结论

AMI 后早期应用 LCZ696 疗效显著,能有效改善心室重构,调节 TGF-β1/Smad3 表达水平,抑制 TGF-β1/Smad3 信号通路,促进心功能和生活质量改善,且安全性良好,值得临床推广应用。本研究的关键发现对理解和管理急性心肌梗死(AMI)具有重要的临床意义。观察组在整体临床疗效、心功能、生化状态、心室结构和功能等方面均表现出显著改善,为 AMI 患者的综合治疗提供了有力证据。这种治疗方法有望成为 AMI 患者治疗和护理策略的重要组成部分,有助于降低心血管风险,改善生活质量,并为未来的 AMI 治疗提供新的研究方向。

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