Suling Ye, Nina Guo, Jie Li, Jinglin Zhao, Dafei Zong, Lili Wang
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引用次数: 0
摘要
目的:比较早期血管紧张素受体-neprilysin抑制剂(ARNI)与血管紧张素转换酶抑制剂或血管紧张素受体阻滞剂(ACEI/ARB)治疗对急性前壁心肌梗死患者左心室重构和心力衰竭进展的影响。方法:按治疗方法将患者分为ARNI组(n=97)和ACEI/ARB组(n=71)。分析基线特征、心脏超声数据(基线、0-3个月、6-12个月)和主要心脏不良事件(mace)。结果:与ACEI/ARB组相比,ARNI组在左室舒张末期直径和相对壁厚方面表现出更大的改善。亚组分析(目标剂量达到者、急诊再灌注接受者、左室射血分数≥50%的患者)一致显示ARNI治疗有更好的改善。ARNI治疗也显著降低mace风险(HR = 0.392, 95% CI: 0.194-0.791, P = 0.009)。结论:与ACEI/ARB相比,ARNI能增强心肌梗死后心功能的保存,减轻不良心室重构,维持心室几何形状。此外,ARNI与主要心脏不良事件的减少和生存结果的改善有关。
Early Sacubitril/valsartan Therapy Reduces Ventricular Remodeling and Cardiac Events in Patients with Acute Anterior Myocardial Infarction.
Purpose: To compare the effects of early angiotensin receptor-neprilysin inhibitor (ARNI) versus angiotensin-converting enzyme inhibitor or angiotensin receptor blocker (ACEI/ARB) therapy on left ventricular remodeling and heart failure progression in patients with acute anterior wall myocardial infarction.
Methods: Patients were stratified by treatment into ARNI (n=97) and ACEI/ARB (n=71) groups. Baseline characteristics, cardiac ultrasound data (baseline, 0-3 months, 6-12 months), and major adverse cardiac events (MACEs) were analyzed.
Results: The ARNI group demonstrated significantly greater improvements in left ventricular end-diastolic diameter and relative wall thickness versus the ACEI/ARB group. Subgroup analyses (target-dose achievers, emergency reperfusion recipients, left ventricular ejection fraction ≥50% patients) consistently showed better improvements with ARNI. ARNI therapy also significantly reduced MACEs risk (HR = 0.392, 95% CI: 0.194-0.791, P = 0.009).
Conclusion: Compared with ACEI/ARB, ARNI demonstrated enhanced preservation of cardiac function, attenuation of adverse ventricular remodeling, and maintenance of ventricular geometry following myocardial infarction. Additionally, ARNI was associated with a reduction in major adverse cardiac events and improved survival outcomes.
期刊介绍:
The European Journal of Pharmacology publishes research papers covering all aspects of experimental pharmacology with focus on the mechanism of action of structurally identified compounds affecting biological systems.
The scope includes:
Behavioural pharmacology
Neuropharmacology and analgesia
Cardiovascular pharmacology
Pulmonary, gastrointestinal and urogenital pharmacology
Endocrine pharmacology
Immunopharmacology and inflammation
Molecular and cellular pharmacology
Regenerative pharmacology
Biologicals and biotherapeutics
Translational pharmacology
Nutriceutical pharmacology.