Asif Midhat, Malik Fatima, Khan Abdul Salar, Zainab Saadia, Ali Muhammad, Shah Ibrahim, Ahmad Mughal Muhammad, Avinash Fnu, Kirshan Kumar Sanjay
Medicine, Khawaja Muhammad Safdar Medical College, Sialkot, PAK.
Obstetrics and Gynecology, Combined Military Hospital, Sialkot, PAK.
Cureus. 2024 Dec 16;16(12):e75786. doi: 10.7759/cureus.75786. eCollection 2024 Dec.
Background Heart failure (HF) is commonly managed by addressing water and sodium (Na) balance, with arterial circulation playing a major role in influencing renal Na and water excretion. Recently, chloride (Cl) has been recognized as an important factor in HF, associated with volume regulation and its modulation of renin-angiotensin-aldosterone system (RAAS) activity through macula densa signaling, which impacts Na retention and neurohormonal activation. Acetazolamide, a carbonic anhydrase inhibitor, can enhance decongestion in HF by increasing urinary Na and Cl excretion when added to loop diuretics, a mechanism supported by prior studies demonstrating improved urine output and decongestion. Objective This study investigates the neurohormonal effects of acetazolamide in acute HF, focusing on its ability to enhance decongestion, reduce neurohormonal activation (e.g., renin and aldosterone), and modulate RAAS markers. Methods In this prospective, single-center observational study, 80 patients with acute HF were enrolled and divided into two groups: a case group (n=40) receiving acetazolamide with standard therapy and a control group (n=40) on standard therapy alone. Patients were matched based on clinical characteristics to reduce selection bias. Baseline characteristics, neurohormonal profiles, including plasma renin activity (PRA) and aldosterone, electrolyte levels, and clinical outcomes were compared. Results The acetazolamide group exhibited higher urinary Cl excretion (108.9±25.3 mEq/L vs. 79.2±22.7 mEq/L; p<0.001) and reduced PRA and aldosterone levels (1.3±0.4 ng/mL/h and 88±21 pg/mL) compared to controls (1.7±0.6 ng/mL/h and 128±29 pg/mL; p=0.002 and p=0.006, respectively). These reductions in PRA and aldosterone are significant as they correlate with improved volume status and reduced neurohormonal stress, which are critical components in HF management. Improved clinical outcomes included a greater percentage of patients becoming symptom-free within 72 hours (77.5% vs. 52.5%; p=0.018) and shorter hospitalization (5.6±1.4 days vs. 7.1±1.7 days; p=0.028). Conclusion Acetazolamide in addition to standard therapy enhances decongestion and reduces neurohormonal activation in acute HF, suggesting its dual benefit in fluid management and neurohormonal modulation. Further research is needed to confirm these benefits, assess long-term effects, and overcome limitations, including the study's single-center observational design.
心力衰竭(HF)的治疗通常侧重于调节水钠平衡,动脉循环在影响肾脏钠和水排泄方面起主要作用。最近,氯离子(Cl)被认为是心力衰竭中的一个重要因素,它与容量调节以及通过致密斑信号对肾素-血管紧张素-醛固酮系统(RAAS)活性的调节有关,这会影响钠潴留和神经激素激活。乙酰唑胺是一种碳酸酐酶抑制剂,当添加到袢利尿剂中时,可通过增加尿钠和氯排泄来增强心力衰竭的消肿作用,先前的研究支持这一机制,这些研究表明尿量增加和消肿效果改善。
本研究调查乙酰唑胺在急性心力衰竭中的神经激素作用,重点关注其增强消肿、降低神经激素激活(如肾素和醛固酮)以及调节RAAS标志物的能力。
在这项前瞻性单中心观察性研究中,80例急性心力衰竭患者入组并分为两组:病例组(n = 40)接受乙酰唑胺联合标准治疗,对照组(n = 40)仅接受标准治疗。根据临床特征进行患者匹配以减少选择偏倚。比较基线特征、神经激素谱,包括血浆肾素活性(PRA)和醛固酮、电解质水平及临床结局。
与对照组相比,乙酰唑胺组尿氯排泄更高(108.9±25.3 mEq/L对79.2±22.7 mEq/L;p<0.001),PRA和醛固酮水平降低(分别为1.3±0.4 ng/mL/h和88±21 pg/mL)(对照组分别为1.7±0.6 ng/mL/h和128±29 pg/mL;p = 0.002和p = 0.006)。PRA和醛固酮的这些降低具有重要意义,因为它们与容量状态改善和神经激素应激降低相关,而这是心力衰竭管理中的关键组成部分。改善的临床结局包括72小时内无症状患者的百分比更高(77.5%对52.5%;p = 0.018)以及住院时间更短(5.6±1.4天对7.1±1.7天;p = 0.028)。
乙酰唑胺联合标准治疗可增强急性心力衰竭的消肿作用并降低神经激素激活,表明其在液体管理和神经激素调节方面具有双重益处。需要进一步研究以证实这些益处、评估长期影响并克服局限性,包括本研究的单中心观察性设计。