急性肾损伤期间允许性氮质血症可使肾脏更快恢复,减少肾纤维化:一项假设和临床发展计划

Lakhmir S Chawla
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引用次数: 0

摘要

急性肾损伤(AKI)的临床前模型一致表明,尿毒症环境可促进肾脏恢复并减少肾脏纤维化。同样,在多项研究和多个物种中都观察到单核细胞/巨噬细胞浸润、补体水平以及损伤肾脏中的其他炎症标志物明显减少。从本质上讲,降低肾脏清除率具有令人惊讶的反直觉效果,是治疗 AKI 的有效方法。在这篇《透视》中,作者提出了一个假设,描述了为什么尿毒症环境对肾脏有保护作用,并建议进行 "允许性氮质血症 "临床试验,以改善严重 AKI 重症患者的肾脏恢复和长期肾脏预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Permissive azotemia during acute kidney injury enables more rapid renal recovery and less renal fibrosis: a hypothesis and clinical development plan.

Permissive azotemia during acute kidney injury enables more rapid renal recovery and less renal fibrosis: a hypothesis and clinical development plan.

Permissive azotemia during acute kidney injury enables more rapid renal recovery and less renal fibrosis: a hypothesis and clinical development plan.

Preclinical models of acute kidney injury (AKI) consistently demonstrate that a uremic milieu enhances renal recovery and decreases kidney fibrosis. Similarly, significant decreases in monocyte/macrophage infiltration, complement levels, and other markers of inflammation in the injured kidney are observed across multiple studies and species. In essence, decreased renal clearance has the surprising and counterintuitive effect of being an effective treatment for AKI. In this Perspective, the author suggests a hypothesis describing why the uremic milieu is kidney protective and proposes a clinical trial of 'permissive azotemia' to improve renal recovery and long-term renal outcomes in critically ill patients with severe AKI.

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