Xie Li, Xiao Han, Zhao Maoyu, Tang Si, Qiu Youzhu
Department of Cardiology, The Second Affiliated Hospital, Army Medical University (Third Military Medical University) Chongqing 400037, China.
Am J Cardiovasc Dis. 2024 Feb 20;14(1):21-28. doi: 10.62347/SYIX9692. eCollection 2024.
To evaluate the impact of varying dosages of Spironolactone on the short-term effectiveness and ventricular remodeling indicators in patients with Heart Failure of Ischemic Cardiomyopathy (HFIC).
A cohort of 141 HFIC patients, admitted to our hospital between October 2018 and February 2023, were enrolled for this study. Alongside the standard treatment for Chronic Congestive Heart Failure (CHF), these patients were randomly assigned to either a low-dose (20 mg/d, N=70) or a high-dose (60 mg/d, N=71) Spironolactone group. After four weeks, various parameters were assessed and compared within each group before and after the treatment. These parameters included echocardiographic indices (LVEF, LVESD, LVEDD, LVESV, and LVEDV), New York Heart Association (NYHA) cardiac function classification, ventricular remodeling markers (hs-CRP, TNF-α, NT-pro BNP, Gal-3, MMP-9, and TIMP-4), and the Six Minute Walk Distance (6MWD).
Both low-dose and high-dose Spironolactone significantly improved LVEF and 6MWD in HFIC patients (<0.05), as well as markedly reduced LVESD, LVEDD, LVESV, LVEDV, and NYHA cardiac function grades (<0.05). The high-dose group exhibited the most pronounced improvements (<0.05). High-dose Spironolactone was more effective in improving the clinical and total effective rate compared to the low-dose, significantly reducing treatment inefficacy (<0.05). Both dosages significantly increased serum potassium levels within normal ranges. They also improved the expression of ventricular remodeling markers (hs-CRP, TNF-α, NT-pro BNP, Gal-3, MMP-9, and TIMP-4) in HFIC patients, with the high-dose group showing the most significant results (<0.05).
High-dose Spironolactone (60 mg/d) demonstrates superior efficacy over the low-dose (20 mg/d) in rapidly diminishing ventricular remodeling damage and enhancing cardiac function and clinical symptoms in HFIC patients over a short duration.
评估不同剂量螺内酯对缺血性心肌病心力衰竭(HFIC)患者短期疗效及心室重构指标的影响。
选取2018年10月至2023年2月期间我院收治的141例HFIC患者纳入本研究。在慢性充血性心力衰竭(CHF)标准治疗的基础上,将这些患者随机分为低剂量(20mg/d,n = 70)或高剂量(60mg/d,n = 71)螺内酯组。四周后,对每组治疗前后的各项参数进行评估和比较。这些参数包括超声心动图指标(左心室射血分数、左心室收缩末期内径、左心室舒张末期内径、左心室收缩末期容积和左心室舒张末期容积)、纽约心脏协会(NYHA)心功能分级、心室重构标志物(超敏C反应蛋白、肿瘤坏死因子-α、N末端B型利钠肽原、半乳糖凝集素-3、基质金属蛋白酶-9和金属蛋白酶组织抑制因子-4)以及六分钟步行距离(6MWD)。
低剂量和高剂量螺内酯均能显著改善HFIC患者的左心室射血分数和6MWD(<0.05),并显著降低左心室收缩末期内径、左心室舒张末期内径、左心室收缩末期容积、左心室舒张末期容积和NYHA心功能分级(<0.05)。高剂量组改善最为明显(<0.05)。与低剂量相比,高剂量螺内酯在提高临床有效率和总有效率方面更有效,显著降低治疗无效情况(<0.05)。两种剂量均能使血清钾水平在正常范围内显著升高。它们还改善了HFIC患者心室重构标志物(超敏C反应蛋白、肿瘤坏死因子-α、N末端B型利钠肽原、半乳糖凝集素-3、基质金属蛋白酶-9和金属蛋白酶组织抑制因子-4)的表达,高剂量组效果最为显著(<0.05)。
高剂量螺内酯(60mg/d)在短期内比低剂量(20mg/d)更能有效减轻HFIC患者的心室重构损伤,增强心功能并改善临床症状。