Fourth Department of Liver Disease, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Department of Microbiology and Infectious Disease Center, School of Basic Medical Sciences, Peking University, Beijing, China.
Gut Liver. 2024 Nov 15;18(6):934-948. doi: 10.5009/gnl240038. Epub 2024 Aug 29.
Ascites is the most common complication in patients with decompensated cirrhosis. This condition results in a severely impaired quality of life, excessive healthcare use, recurrent hospitalizations and significant morbidity and mortality. While loop diuretics and mineralocorticoid receptor antagonists are commonly employed for symptom relief, our understanding of their impact on survival remains limited. A comprehensive understanding of the underlying pathophysiological mechanism of ascites is crucial for its optimal management. The renin-angiotensin-aldosterone system (RAAS) is increasingly believed to play a pivotal role in the formation of cirrhotic ascites, as RAAS overactivation leads to a reduction in urine sodium excretion then a decrease in the ability of the kidneys to excrete water. In this review, the authors provide an overview of the pathogenesis of cirrhotic ascites, the challenges associated with current pharmacologic treatments, and the previous attempts to modulate the RAAS, followed by a description of some emerging targeted RAAS agents with the potential to be used to treat ascites.
腹水是失代偿期肝硬化患者最常见的并发症。这种情况导致生活质量严重受损、医疗保健过度使用、反复住院以及发病率和死亡率显著增加。虽然螺内酯和盐皮质激素受体拮抗剂常用于缓解症状,但我们对其对生存的影响的了解仍然有限。腹水的最佳管理需要对其潜在的病理生理机制有全面的了解。肾素-血管紧张素-醛固酮系统(RAAS)在肝硬化腹水的形成中被认为起着关键作用,因为 RAAS 的过度激活导致尿钠排泄减少,随后肾脏排出水分的能力下降。在这篇综述中,作者概述了肝硬化腹水的发病机制、当前药物治疗相关的挑战以及以前对 RAAS 的调节尝试,随后描述了一些新兴的靶向 RAAS 药物,这些药物有可能用于治疗腹水。