Understanding acute kidney injury in cirrhosis: Current perspective.

IF 2.5 Q2 GASTROENTEROLOGY & HEPATOLOGY
Sayan Malakar, Sumit Rungta, Arghya Samanta, Umair Shamsul Hoda, Piyush Mishra, Gaurav Pande, Akash Roy, Suprabhat Giri, Praveer Rai, Samir Mohindra, Uday C Ghoshal
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Abstract

Acute kidney injury (AKI) is present in 30%-40% of hospitalized patients with cirrhosis. Its incidence is higher in patients with severe alcoholic hepatitis, spontaneous bacterial peritonitis, and acute-on-chronic-liver failure (ACLF). Kidney injury is an important landmark event in the natural history of cirrhosis as it is associated with higher mortality. Overwhelming systemic vasodilation, cardiac dysfunction, hypoperfusion, endotoxemia, and direct nephrotoxicity predispose patients with cirrhosis to kidney injury. Infection is present in 25% of patients with decompensated cirrhosis and 35%-40% of patients with ACLF. Advanced cirrhosis with portal hypertension leads to a sluggish portal flow, leading to increased gut congestion, altered gut permeability and bacterial translocations. They drive infection and endotoxemia in such patients. Pathogen-associated molecular patterns activate inflammatory cascades, which leads to further deterioration in hemodynamics and reduced glomerular filtration rate. Infections and pro-inflammatory cytokines like interleukin 6 (IL-6), IL-1, and tumor necrosis factor alpha may directly cause kidney parenchymal injury. The combined effect of dysfunctional albumin and systemic and splanchnic vasodilatation leads to low effective blood volume, activating the renin-angiotensin-aldosterone system. This causes renal vasoconstriction, water retention, and ascites, which progresses to hepatorenal physiology and AKI development. Vasoconstriction and volume expansion effectively improve arterial blood volume and systemic hemodynamics, thereby improving renal blood flow. It is of paramount importance to predict, detect, and treat AKI in its early state, as progressive renal dysfunction is invariably associated with higher mortality in patients with decompensated cirrhosis and ACLF. This comprehensive review will focus on the recent evolving concepts of the pathophysiology, diagnosis, and management of AKI in patients with cirrhosis.

理解肝硬化急性肾损伤:当前观点。
30%-40%的肝硬化住院患者存在急性肾损伤(AKI)。在严重酒精性肝炎、自发性细菌性腹膜炎和急性慢性肝衰竭(ACLF)患者中发病率较高。肾损伤是肝硬化自然史上一个重要的里程碑事件,因为它与较高的死亡率相关。压倒性的全身性血管扩张、心功能障碍、低灌注、内毒素血症和直接肾毒性使肝硬化患者易发生肾损伤。25%的失代偿性肝硬化患者和35%-40%的ACLF患者存在感染。晚期肝硬化合并门静脉高压症导致门静脉血流缓慢,导致肠道充血增加,肠道通透性改变和细菌易位。它们在这些患者中引起感染和内毒素血症。病原体相关的分子模式激活炎症级联反应,导致血流动力学进一步恶化和肾小球滤过率降低。感染和白细胞介素6 (IL-6)、IL-1、肿瘤坏死因子α等促炎因子可直接引起肾实质损伤。功能失调的白蛋白与全身和内脏血管扩张的共同作用导致有效血容量低,激活肾素-血管紧张素-醛固酮系统。这会导致肾血管收缩、水潴留和腹水,进而发展为肝肾生理和AKI的发展。血管收缩和体积扩张有效改善动脉血容量和全身血流动力学,从而改善肾血流量。早期预测、检测和治疗AKI是至关重要的,因为进行性肾功能障碍总是与失代偿性肝硬化和ACLF患者的高死亡率相关。这篇全面的综述将集中在肝硬化患者AKI的病理生理学、诊断和管理的最新发展概念。
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来源期刊
World Journal of Hepatology
World Journal of Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
4.10
自引率
4.20%
发文量
172
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