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重症监护病房急性肾损伤的精准管理:现状。

Precision management of acute kidney injury in the intensive care unit: current state of the art.

机构信息

Division of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

Department of Nephrology, Prince of Wales Clinical School, UNSW Medicine, Sydney, NSW, Australia.

出版信息

Intensive Care Med. 2023 Sep;49(9):1049-1061. doi: 10.1007/s00134-023-07171-z. Epub 2023 Aug 8.

Abstract

Acute kidney injury (AKI) is a prototypical example of a common syndrome in critical illness defined by consensus. The consensus definition for AKI, traditionally defined using only serum creatinine and urine output, was needed to standardize the description for epidemiology and to harmonize eligibility for clinical trials. However, AKI is not a simple disease, but rather a complex and multi-factorial syndrome characterized by a wide spectrum of pathobiology. AKI is now recognized to be comprised of numerous sub-phenotypes that can be discriminated through shared features such as etiology, prognosis, or common pathobiological mechanisms of injury and damage. The characterization of sub-phenotypes can serve to enable prognostic enrichment (i.e., identify subsets of patients more likely to share an outcome of interest) and predictive enrichment (identify subsets of patients more likely to respond favorably to a given therapy). Existing and emerging biomarkers will aid in discriminating sub-phenotypes of AKI, facilitate expansion of diagnostic criteria, and be leveraged to realize personalized approaches to management, particularly for recognizing treatment-responsive mechanisms (i.e., endotypes) and targets for intervention (i.e., treatable traits). Specific biomarkers (e.g., serum renin; olfactomedin 4 (OLFM4); interleukin (IL)-9) may further enable identification of pathobiological mechanisms to serve as treatment targets. However, even non-specific biomarkers of kidney injury (e.g., neutrophil gelatinase-associated lipocalin, NGAL; [tissue inhibitor of metalloproteinases 2, TIMP2]·[insulin like growth factor binding protein 7, IGFBP7]; kidney injury molecule 1, KIM-1) can direct greater precision management for specific sub-phenotypes of AKI. This review will summarize these evolving concepts and recent innovations in precision medicine approaches to the syndrome of AKI in critical illness, along with providing examples of how they can be leveraged to guide patient care.

摘要

急性肾损伤(AKI)是一种典型的综合征,在重症疾病中被定义为共识。传统上仅使用血清肌酐和尿量定义 AKI 的共识定义,是为了标准化描述以进行流行病学研究,并协调临床试验的资格。然而,AKI 不是一种简单的疾病,而是一种复杂的多因素综合征,其特点是病理生物学谱广泛。现在已经认识到,AKI 由许多亚表型组成,这些亚表型可以通过共同的特征(如病因、预后或共同的病理生物学损伤和损伤机制)来区分。亚表型的特征可以用于实现预后富集(即,确定更有可能具有共同感兴趣的结果的亚组患者)和预测性富集(确定更有可能对特定治疗反应良好的亚组患者)。现有的和新兴的生物标志物将有助于区分 AKI 的亚表型,促进诊断标准的扩展,并用于实现个性化管理方法,特别是用于识别治疗反应机制(即,内型)和干预目标(即,可治疗特征)。特定的生物标志物(例如,血清肾素;olfactomedin 4(OLFM4);白细胞介素(IL)-9)可能进一步有助于确定作为治疗目标的病理生物学机制。然而,即使是肾脏损伤的非特异性生物标志物(例如,中性粒细胞明胶酶相关脂质运载蛋白,NGAL;[金属蛋白酶抑制剂 2,TIMP2]·[胰岛素样生长因子结合蛋白 7,IGFBP7];肾损伤分子 1,KIM-1)也可以指导 AKI 特定亚表型的更精确管理。这篇综述将总结这些不断发展的概念和重症疾病 AKI 综合征精准医学方法的最新创新,以及提供如何利用这些方法来指导患者护理的示例。

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